Academic Journal

Epigenetic dynamics of cellular senescence: From mechanistic insights to precision senotherapy.

Λεπτομέρειες βιβλιογραφικής εγγραφής
Τίτλος: Epigenetic dynamics of cellular senescence: From mechanistic insights to precision senotherapy.
Συγγραφείς: Hu X; Department of Nephrology, Institute of Kidney Diseases, West China Hospital of Sichuan University, Chengdu, Sichuan 610041, China.; West China School of Medicine, Sichuan University, Chengdu, Sichuan 610041, China., Lai W; Department of Nephrology, The Key Laboratory for the Prevention and Treatment of Kidney Disease of Chongqing, Chongqing Clinical Research Center of Kidney and Urology Diseases, Xinqiao Hospital, Army Medical University (Third Military Medical University), Chongqing 400037, China., Liu M; Department of Anesthesiology, Air Force Hospital of Western Theater Command, PLA, Chengdu, Sichuan 610011, China., Wang B; Department of Nephrology, Institute of Kidney Diseases, West China Hospital of Sichuan University, Chengdu, Sichuan 610041, China.; West China School of Medicine, Sichuan University, Chengdu, Sichuan 610041, China.
Πηγή: Chinese medical journal [Chin Med J (Engl)] 2026 Jul 05; Vol. 139 (13), pp. 1913-1942. Date of Electronic Publication: 2026 Mar 17.
Τύπος έκδοσης: Journal Article; Review
Γλώσσα: English
Στοιχεία περιοδικού: Publisher: Chinese Medical Association ; produced by Wolters Kluwer Country of Publication: China NLM ID: 7513795 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 2542-5641 (Electronic) Linking ISSN: 03666999 NLM ISO Abbreviation: Chin Med J (Engl) Subsets: MEDLINE
Imprint Name(s): Publication: <2015- > : Beijing : Chinese Medical Association ; produced by Wolters Kluwer
Original Publication: Peking, Chinese Medical Assn.
Ιατρικοί όροι (MeSH): Cellular Senescence*/genetics , Cellular Senescence*/physiology , Epigenesis, Genetic*/genetics , Senotherapeutics*, DNA Methylation/genetics ; Humans ; Animals
Περίληψη: Abstract: Cellular senescence functions as a pivotal stress response with dual roles; it serves as a barrier against early tumorigenesis while paradoxically driving late-stage tumor progression and the pathogenesis of many other age-related diseases, including cardiovascular, neurodegenerative, metabolic, and fibrotic disorders. This review comprehensively elucidates how the senescent phenotype is orchestrated by a dynamic epigenetic landscape. We detail how dysregulation in chromatin remodeling (e.g., heterochromatin loss), histone modifications, DNA methylation, and the epitranscriptome rewrites genome architecture to govern the initiation and maintenance of the senescent phenotype within these specific disease contexts. Crucially, we highlight the profound heterogeneity of senescence across different pathologies, contrasting its detrimental role in driving tissue degeneration in organs like the lung and kidney against its context-dependent beneficial effects, such as limiting fibrosis in the liver. Furthermore, we evaluate the translational potential of epigenetic drugs-categorized by targets such as DNA methyltransferases (DNMTs), histone methyltransferases (HMTs), and histone deacetylases (HDACs)-as dual-purpose therapeutics. Unlike genetic mutations, epigenetic alterations are reversible. We discuss strategies to either enforce senescence barriers for cancer suppression (pro-senescence) or reverse epigenetic aging signatures for tissue rejuvenation (anti-senescence). This review proposes a roadmap for leveraging epigenetic plasticity, offering a precision medicine approach to target specific senescent cell populations and extend health span.
(Copyright © 2026 The Chinese Medical Association, produced by Wolters Kluwer, Inc. under the CC-BY-NC-ND license.)
References: Burdusel D, Doeppner TR, Surugiu R, Hermann DM, Olaru DG, Popa-Wagner A. The intersection of epigenetics and senolytics in mechanisms of aging and therapeutic approaches. Biomolecules 2024;15:18. doi: 10.3390/biom15010018. (PMID: 10.3390/biom15010018)
Shi M, Li H, Liang R, Lin H, Tang Q. The transcription factor STAT3 and aging: An intermediate medium. Biogerontology 2025;26:55. doi: 10.1007/s10522-025-10193-3. (PMID: 10.1007/s10522-025-10193-3)
de Magalhães JP. Cellular senescence in normal physiology. Science 2024;384:1300-1301. doi: 10.1126/science.adj7050. (PMID: 10.1126/science.adj7050)
Huna A, Massemin A, Makulyte G, Flaman JM, Martin N, Bernard D. Regulation of cell function and identity by cellular senescence. J Cell Biol 2024;223:e202401112. doi: 10.1083/jcb.202401112. (PMID: 10.1083/jcb.202401112)
Di Micco R, Krizhanovsky V, Baker D, d’Adda di Fagagna F. Cellular senescence in ageing: From mechanisms to therapeutic opportunities. Nat Rev Mol Cell Biol 2021;22:75-95. doi: 10.1038/s41580-020-00314-w. (PMID: 10.1038/s41580-020-00314-w)
Zhou L, Ma B, Ruscetti M. Cellular senescence offers distinct immunological vulnerabilities in cancer. Trends in Cancer 2025;11:334-350. doi: 10.1016/j.trecan.2024.11.010. (PMID: 10.1016/j.trecan.2024.11.010)
Yang JH, Hayano M, Griffin PT, Amorim JA, Bonkowski MS, Apostolides JK, et al. Loss of epigenetic information as a cause of mammalian aging. Cell 2023;186:305-326. doi: 10.1016/j.cell.2022.12.027. (PMID: 10.1016/j.cell.2022.12.027)
Hayflick L, Moorhead PS. The serial cultivation of human diploid cell strains. Exp Cell Res 1961;25:585-621. doi: 10.1016/0014-4827(61)90192-6. (PMID: 10.1016/0014-4827(61)90192-6)
Harley CB, Futcher AB, Greider CW. Telomeres shorten during ageing of human fibroblasts. Nature 1990;345:458-460. doi: 10.1038/345458a0. (PMID: 10.1038/345458a0)
Chen Q, Fischer A, Reagan JD, Yan LJ, Ames BN. Oxidative DNA damage and senescence of human diploid fibroblast cells. Proc Natl Acad Sci USA 1995;92:4337-4341. doi: 10.1073/pnas.92.10.4337. (PMID: 10.1073/pnas.92.10.4337)
Serrano M, Lin AW, McCurrach ME, Beach D, Lowe SW. Oncogenic ras provokes premature cell senescence associated with accumulation of p53 and p16INK4a. Cell 1997;88:593-602. doi: 10.1016/s0092-8674(00)81902-9. (PMID: 10.1016/s0092-8674(00)81902-9)
Wang B, Han J, Elisseeff JH, Demaria M. The senescence-associated secretory phenotype and its physiological and pathological implications. Nat Rev Mol Cell Biol 2024;25:958-978. doi: 10.1038/s41580-024-00727-x. (PMID: 10.1038/s41580-024-00727-x)
Dimri GP, Lee X, Basile G, Acosta M, Scott G, Roskelley C, et al. A biomarker that identifies senescent human cells in culture and in aging skin in vivo . Proc Natl Acad Sci U S A 1995;92:9363-9367. doi: 10.1073/pnas.92.20.9363. (PMID: 10.1073/pnas.92.20.9363)
Narita M, Nũnez S, Heard E, Narita M, Lin AW, Hearn SA, et al. Rb-mediated heterochromatin formation and silencing of E2F target genes during cellular senescence. Cell 2003;113:703-716. doi: 10.1016/s0092-8674(03)00401-x. (PMID: 10.1016/s0092-8674(03)00401-x)
Bodnar AG, Ouellette M, Frolkis M, Holt SE, Chiu CP, Morin GB, et al. Extension of life-span by introduction of telomerase into normal human cells. Science 1998;279:349-352. doi: 10.1126/science.279.5349.349. (PMID: 10.1126/science.279.5349.349)
Smith JR, Pereira-Smith OM. Replicative senescence: Implications for in vivo aging and tumor suppression. Science 1996;273:63-67. doi: 10.1126/science.273.5271.63. (PMID: 10.1126/science.273.5271.63)
López-Otín C, Blasco MA, Partridge L, Serrano M, Kroemer G. The hallmarks of aging. Cell 2013;153:1194-1217. doi: 10.1016/j.cell.2013.05.039. (PMID: 10.1016/j.cell.2013.05.039)
Zhu Y, Tchkonia T, Pirtskhalava T, Gower AC, Ding H, Giorgadze N, et al. The Achilles’ heel of senescent cells: From transcriptome to senolytic drugs. Aging Cell 2015;14:644-658. doi: 10.1111/acel.12344. (PMID: 10.1111/acel.12344)
Chang J, Wang Y, Shao L, Laberge RM, Demaria M, Campisi J, et al. Clearance of senescent cells by ABT263 rejuvenates aged hematopoietic stem cells in mice. Nat Med 2016;22:78-83. doi: 10.1038/nm.4010. (PMID: 10.1038/nm.4010)
Xu M, Pirtskhalava T, Farr JN, Weigand BM, Palmer AK, Weivoda MM, et al. Senolytics improve physical function and increase lifespan in old age. Nat Med 2018;24:1246-1256. doi: 10.1038/s41591-018-0092-9. (PMID: 10.1038/s41591-018-0092-9)
Justice JN, Nambiar AM, Tchkonia T, LeBrasseur NK, Pascual R, Hashmi SK, et al. Senolytics in idiopathic pulmonary fibrosis: Results from a first-in-human, open-label, pilot study. EBioMedicine 2019;40:554-563. doi: 10.1016/j.ebiom.2018.12.052. (PMID: 10.1016/j.ebiom.2018.12.052)
Coppé JP, Patil CK, Rodier F, Sun Y, Muñoz DP, Goldstein J, et al. Senescence-associated secretory phenotypes reveal cell-nonautonomous functions of oncogenic RAS and the p53 tumor suppressor. PLoS Biol 2008;6:2853-2868. doi: 10.1371/journal.pbio.0060301. (PMID: 10.1371/journal.pbio.0060301)
Kuilman T, Michaloglou C, Vredeveld LCW, Douma S, van Doorn R, Desmet CJ, et al. Oncogene-induced senescence relayed by an interleukin-dependent inflammatory network. Cell 2008;133:1019-1031. doi: 10.1016/j.cell.2008.03.039. (PMID: 10.1016/j.cell.2008.03.039)
Acosta JC, O’Loghlen A, Banito A, Guijarro MV, Augert A, Raguz S, et al. Chemokine signaling via the CXCR2 receptor reinforces senescence. Cell 2008;133:1006-1018. doi: 10.1016/j.cell.2008.03.038. (PMID: 10.1016/j.cell.2008.03.038)
Short S, Fielder E, Miwa S, von Zglinicki T. Senolytics and senostatics as adjuvant tumour therapy. EBioMedicine 2019;41:683-692. doi: 10.1016/j.ebiom.2019.01.056. (PMID: 10.1016/j.ebiom.2019.01.056)
Kim NW, Piatyszek MA, Prowse KR, Harley CB, West MD, Ho PL, et al. Specific association of human telomerase activity with immortal cells and cancer. Science 1994;266:2011-2015. doi: 10.1126/science.7605428. (PMID: 10.1126/science.7605428)
Braig M, Lee S, Loddenkemper C, Rudolph C, Peters AH, Schlegelberger B, et al. Oncogene-induced senescence as an initial barrier in lymphoma development. Nature 2005;436:660-665. doi: 10.1038/nature03841. (PMID: 10.1038/nature03841)
Michaloglou C, Vredeveld LC, Soengas MS, Denoyelle C, Kuilman T, van der Horst CMAM, et al. BRAFE600-associated senescence-like cell cycle arrest of human naevi. Nature 2005;436:720-724. doi: 10.1038/nature03890. (PMID: 10.1038/nature03890)
Halazonetis TD, Gorgoulis VG, Bartek J. An oncogene-induced DNA damage model for cancer development. Science 2008;319:1352-1355. doi: 10.1126/science.1140735. (PMID: 10.1126/science.1140735)
Hanahan D. Hallmarks of Cancer: New dimensions. Cancer Discov 2022;12:31-46. doi: 10.1158/2159-8290.CD-21-1059. (PMID: 10.1158/2159-8290.CD-21-1059)
Zhang L, Pitcher LE, Yousefzadeh MJ, Niedernhofer LJ, Robbins PD, Zhu Y. Cellular senescence: A key therapeutic target in aging and diseases. J Clin Invest 2022;132:e158450. doi: 10.1172/JCI158450. (PMID: 10.1172/JCI158450)
Huang W, Hickson LJ, Eirin A, Kirkland JL, Lerman LO. Cellular senescence: The good, the bad and the unknown. Nat Rev Nephrol 2022;18:611-627. doi: 10.1038/s41581-022-00601-z. (PMID: 10.1038/s41581-022-00601-z)
Wu Z, Qu J, Liu GH. Roles of chromatin and genome instability in cellular senescence and their relevance to ageing and related diseases. Nat Rev Mol Cell Biol 2024;25:979-1000. doi: 10.1038/s41580-024-00775-3. (PMID: 10.1038/s41580-024-00775-3)
Petr MA, Tulika T, Carmona-Marin LM, Scheibye-Knudsen M. Protecting the Aging Genome. Trends Cell Biol 2020;30:117-132. doi: 10.1016/j.tcb.2019.12.001. (PMID: 10.1016/j.tcb.2019.12.001)
Ullah A, Arif M, Waqas M, Hasnain M, Saira A, Tariq R, et al. Exploring the role of chemicals and environmental factors for cancer proliferation. Open Access Library Journal 2024;11:1-19. doi: 10.4236/oalib.1112607. (PMID: 10.4236/oalib.1112607)
Lee JH, Paull TT. Cellular functions of the protein kinase ATM and their relevance to human disease. Nat Rev Mol Cell Biol 2021;22:796-814. doi: 10.1038/s41580-021-00394-2. (PMID: 10.1038/s41580-021-00394-2)
Kumari R, Jat P. Mechanisms of cellular senescence: Cell cycle arrest and senescence associated secretory phenotype. Front Cell Dev Biol 2021;9:645593. doi: 10.3389/fcell.2021.645593. (PMID: 10.3389/fcell.2021.645593)
Feng T, Xie F, Lee L, Lin Z, Tu Y, Lyu Y, et al. Cellular senescence in cancer: From mechanism paradoxes to precision therapeutics. Mol Cancer 2025;24:213. doi: 10.1186/s12943-025-02419-2. (PMID: 10.1186/s12943-025-02419-2)
Safwan-Zaiter H, Wagner N, Wagner KD. P16INK4A-more than a senescence marker. Life (Basel) 2022;12:1332. doi: 10.3390/life12091332. (PMID: 10.3390/life12091332)
Mehdizadeh M, Aguilar M, Thorin E, Ferbeyre G, Nattel S. The role of cellular senescence in cardiac disease: Basic biology and clinical relevance. Nat Rev Cardiol 2022;19:250-264. doi: 10.1038/s41569-021-00624-2. (PMID: 10.1038/s41569-021-00624-2)
Zhao S, Qiao Z, Pfeifer R, Pape HC, Mao K, Tang H, et al. Modulation of fracture healing by senescence-associated secretory phenotype (SASP): A narrative review of the current literature. Eur J Med Res 2024;29:38. doi: 10.1186/s40001-023-01604-7. (PMID: 10.1186/s40001-023-01604-7)
Kolesnichenko M, Mikuda N, Höpken UE, Kärgel E, Uyar B, Tufan AB, et al. Transcriptional repression of NFKBIA triggers constitutive IKK- and proteasome-independent p65/RelA activation in senescence. EMBO J 2021;40:e104296. doi: 10.15252/embj.2019104296. (PMID: 10.15252/embj.2019104296)
Takahashi A, Loo TM, Okada R, Kamachi F, Watanabe Y, Wakita M, et al. Downregulation of cytoplasmic DNases is implicated in cytoplasmic DNA accumulation and SASP in senescent cells. Nat Commun 2018;9:1249. doi: 10.1038/s41467-018-03555-8. (PMID: 10.1038/s41467-018-03555-8)
Victorelli S, Salmonowicz H, Chapman J, Martini H, Vizioli MG, Riley JS, et al. Apoptotic stress causes mtDNA release during senescence and drives the SASP. Nature 2023;622:627-636. doi: 10.1038/s41586-023-06621-4. (PMID: 10.1038/s41586-023-06621-4)
Zhang X, Zhuang M, Zhang H, Zhu Y, Yang J, Wu X, et al. Melatonin-mediated cGAS-STING signal in senescent macrophages promote TNBC chemotherapy resistance and drive the SASP. J Biol Chem 2025;301:108438. doi: 10.1016/j.jbc.2025.108438. (PMID: 10.1016/j.jbc.2025.108438)
Hao W, Shan W, Wan F, Luo J, Niu Y, Zhou J, et al. Canagliflozin delays aging of HUVECs induced by palmitic acid via the ROS/p38/JNK pathway. Antioxidants (Basel) 2023;12:838. doi: 10.3390/antiox12040838. (PMID: 10.3390/antiox12040838)
Mazzucco AE, Smogorzewska A, Kang C, Luo J, Schlabach MR, Xu Q, et al. Genetic interrogation of replicative senescence uncovers a dual role for USP28 in coordinating the p53 and GATA4 branches of the senescence program. Genes Dev 2017;31:1933-1938. doi: 10.1101/gad.304857.117. (PMID: 10.1101/gad.304857.117)
Herranz N, Gallage S, Mellone M, Wuestefeld T, Klotz S, Hanley CJ, et al. mTOR regulates MAPKAPK2 translation to control the senescence-associated secretory phenotype. Nat Cell Biol 2015;17:1205-1217. doi: 10.1038/ncb3225. (PMID: 10.1038/ncb3225)
Laberge RM, Sun Y, Orjalo AV, Patil CK, Freund A, Zhou L, et al. MTOR regulates the pro-tumorigenic senescence-associated secretory phenotype by promoting IL1A translation. Nat Cell Biol 2015;17:1049-1061. doi: 10.1038/ncb3195. (PMID: 10.1038/ncb3195)
Ito Y, Hoare M, Narita M. Spatial and temporal control of senescence. Trends Cell Biol 2017;27:820-832. doi: 10.1016/j.tcb.2017.07.004. (PMID: 10.1016/j.tcb.2017.07.004)
Suryadevara V, Hudgins AD, Rajesh A, Pappalardo A, Karpova A, Dey AK, et al. SenNet recommendations for detecting senescent cells in different tissues. Nat Rev Mol Cell Biol 2024;25:1001-1023. doi: 10.1038/s41580-024-00738-8. (PMID: 10.1038/s41580-024-00738-8)
Marescal O, Cheeseman IM. Cellular mechanisms and regulation of quiescence. Dev Cell 2020;55:259-271. doi: 10.1016/j.devcel.2020.09.029. (PMID: 10.1016/j.devcel.2020.09.029)
Triana-Martínez F, Loza MI, Domínguez E. Beyond tumor suppression: Senescence in cancer stemness and tumor dormancy. Cells 2020;9:346. doi: 10.3390/cells9020346. (PMID: 10.3390/cells9020346)
Reimann M, Lee S, Schmitt CA. Cellular senescence: Neither irreversible nor reversible. J Exp Med 2024;221:e20232136. doi: 10.1084/jem.20232136. (PMID: 10.1084/jem.20232136)
Chen HA, Ho YJ, Mezzadra R, Adrover JM, Smolkin R, Zhu C, et al. Senescence rewires microenvironment sensing to facilitate antitumor immunity. Cancer Discov 2023;13:432-453. doi: 10.1158/2159-8290.CD-22-0528. (PMID: 10.1158/2159-8290.CD-22-0528)
Martínez-Zamudio RI, Stefa A, Nabuco Leva Ferreira Freitas JA, Vasilopoulos T, Simpson M, Doré G, et al. Escape from oncogene-induced senescence is controlled by POU2F2 and memorized by chromatin scars. Cell Genom 2023;3:100293. doi: 10.1016/j.xgen.2023.100293. (PMID: 10.1016/j.xgen.2023.100293)
Carozzi F, Confortini M, Dalla Palma P, Del Mistro A, Gillio-Tos A, De Marco L, et al. Use of p16-INK4A overexpression to increase the specificity of human papillomavirus testing: A nested substudy of the NTCC randomised controlled trial. Lancet Oncol 2008;9:937-945. doi: 10.1016/S1470-2045(08)70208-0. (PMID: 10.1016/S1470-2045(08)70208-0)
Yu Q, Walters HE, Pasquini G, Pal Singh S, Lachnit M, Oliveira CR, et al. Cellular senescence promotes progenitor cell expansion during axolotl limb regeneration. Dev Cell 2023;58:2416-2427.e7. doi: 10.1016/j.devcel.2023.09.009. (PMID: 10.1016/j.devcel.2023.09.009)
Utikal J, Polo JM, Stadtfeld M, Maherali N, Kulalert W, Walsh RM, et al. Immortalization eliminates a roadblock during cellular reprogramming into iPS cells. Nature 2009;460:1145-1148. doi: 10.1038/nature08285. (PMID: 10.1038/nature08285)
Gonzalez-Meljem JM, Haston S, Carreno G, Apps JR, Pozzi S, Stache C, et al. Stem cell senescence drives age-attenuated induction of pituitary tumours in mouse models of paediatric craniopharyngioma. Nat Commun 2017;8:1819. doi: 10.1038/s41467-017-01992-5. (PMID: 10.1038/s41467-017-01992-5)
Wallis R, Mizen H, Bishop CL. The bright and dark side of extracellular vesicles in the senescence-associated secretory phenotype. Mech Ageing Dev 2020;189:111263. doi: 10.1016/j.mad.2020.111263. (PMID: 10.1016/j.mad.2020.111263)
Takasugi M, Okada R, Takahashi A, Virya Chen D, Watanabe S, Hara E. Small extracellular vesicles secreted from senescent cells promote cancer cell proliferation through EphA2. Nat Commun 2017;8:15729. doi: 10.1038/ncomms15728. (PMID: 10.1038/ncomms15728)
Chaib S, Tchkonia T, Kirkland JL. Cellular senescence and senolytics: The path to the clinic. Nat Med 2022;28:1556-1568. doi: 10.1038/s41591-022-01923-y. (PMID: 10.1038/s41591-022-01923-y)
Feng X, Wang L, Zhou R, Zhou R, Chen L, Peng H, et al. Senescent immune cells accumulation promotes brown adipose tissue dysfunction during aging. Nat Commun 2023;14:3208. doi: 10.1038/s41467-023-38842-6. (PMID: 10.1038/s41467-023-38842-6)
Acosta JC, Banito A, Wuestefeld T, Georgilis A, Janich P, Morton JP, et al. A complex secretory program orchestrated by the inflammasome controls paracrine senescence. Nat Cell Biol 2013;15:978-990. doi: 10.1038/ncb2784. (PMID: 10.1038/ncb2784)
Storer M, Mas A, Robert-Moreno A, Pecoraro M, Ortells MC, Di Giacomo V, et al. Senescence is a developmental mechanism that contributes to embryonic growth and patterning. Cell 2013;155:1119-1130. doi: 10.1016/j.cell.2013.10.041. (PMID: 10.1016/j.cell.2013.10.041)
Demaria M, Ohtani N, Youssef SA, Rodier F, Toussaint W, Mitchell JR, et al. An essential role for senescent cells in optimal wound healing through secretion of PDGF-AA. Dev Cell 2014;31:722-733. doi: 10.1016/j.devcel.2014.11.012. (PMID: 10.1016/j.devcel.2014.11.012)
Veldhoen M, Hocking RJ, Atkins CJ, Locksley RM, Stockinger B. TGFbeta in the context of an inflammatory cytokine milieu supports de novo differentiation of IL-17-producing T cells. Immunity 2006;24:179-189. doi: 10.1016/j.immuni.2006.01.001. (PMID: 10.1016/j.immuni.2006.01.001)
Massagué J, Sheppard D. TGF-β signaling in health and disease. Cell 2023;186:4007-4037. doi: 10.1016/j.cell.2023.07.036. (PMID: 10.1016/j.cell.2023.07.036)
Wang AP, Yang F, Tian Y, Su JH, Gu Q, Chen W, et al. Pulmonary artery smooth muscle cell senescence promotes the proliferation of PASMCs by paracrine IL-6 in hypoxia-induced pulmonary hypertension. Front Physiol 2021;12:656139. doi: 10.3389/fphys.2021.656139. (PMID: 10.3389/fphys.2021.656139)
Sturmlechner I, Zhang C, Sine CC, van Deursen EJ, Jeganathan KB, Hamada N, et al. p21 produces a bioactive secretome that places stressed cells under immunosurveillance. Science 2021;374:eabb3420. doi: 10.1126/science.abb3420. (PMID: 10.1126/science.abb3420)
Trastus LA, d’Adda di Fagagna F. The complex interplay between aging and cancer. Nat Aging 2025;5:350-365. doi: 10.1038/s43587-025-00827-z. (PMID: 10.1038/s43587-025-00827-z)
Li X, Li C, Zhang W, Wang Y, Qian P, Huang H. Inflammation and aging: Signaling pathways and intervention therapies. Signal Transduct Target Ther 2023;8:239. doi: 10.1038/s41392-023-01502-8. (PMID: 10.1038/s41392-023-01502-8)
Liu X, Gu Y, Kumar S, Amin S, Guo Q, Wang J, et al. Oxylipin-PPARγ-initiated adipocyte senescence propagates secondary senescence in the bone marrow. Cell Metab 2023;35:667-684.e6. doi: 10.1016/j.cmet.2023.03.005. (PMID: 10.1016/j.cmet.2023.03.005)
Khalilgharibi N, Mao Y. To form and function: On the role of basement membrane mechanics in tissue development, homeostasis and disease. Open Biol 2021;11:200360. doi: 10.1098/rsob.200360. (PMID: 10.1098/rsob.200360)
Amor C, Fernández-Maestre I, Chowdhury S, Ho YJ, Nadella S, Graham C, et al. Prophylactic and long-lasting efficacy of senolytic CAR T cells against age-related metabolic dysfunction. Nat Aging 2024;4:336-349. doi: 10.1038/s43587-023-00560-5. (PMID: 10.1038/s43587-023-00560-5)
Chen C, Xu ZQ, Zong YP, Ou BC, Shen XH, Feng H, et al. CXCL5 induces tumor angiogenesis via enhancing the expression of FOXD1 mediated by the AKT/NF-κB pathway in colorectal cancer. Cell Death Dis 2019;10:178. doi: 10.1038/s41419-019-1431-6. (PMID: 10.1038/s41419-019-1431-6)
Chambers ES, Vukmanovic-Stejic M, Shih BB, Trahair H, Subramanian P, Devine OP, et al. Recruitment of inflammatory monocytes by senescent fibroblasts inhibits antigen-specific tissue immunity during human aging. Nat Aging 2021;1:101-113. doi: 10.1038/s43587-020-00010-6. (PMID: 10.1038/s43587-020-00010-6)
Eggert T, Wolter K, Ji J, Ma C, Yevsa T, Klotz S, et al. Distinct functions of senescence-associated immune responses in liver tumor surveillance and tumor progression. Cancer Cell 2016;30:533-547. doi: 10.1016/j.ccell.2016.09.003. (PMID: 10.1016/j.ccell.2016.09.003)
Basisty N, Kale A, Jeon OH, Kuehnemann C, Payne T, Rao C, et al. A proteomic atlas of senescence-associated secretomes for aging biomarker development. PLoS Biol 2020;18:e3000599. doi: 10.1371/journal.pbio.3000599. (PMID: 10.1371/journal.pbio.3000599)
Curnock R, Yalci K, Palmfeldt J, Jäättelä M, Liu B, Carroll B. TFEB-dependent lysosome biogenesis is required for senescence. EMBO J 2023;42:e111241. doi: 10.15252/embj.2022111241. (PMID: 10.15252/embj.2022111241)
Feng B, Chu F, Bi A, Huang X, Fang Y, Liu M, et al. Fidelity-oriented fluorescence imaging probes for beta-galactosidase: From accurate diagnosis to precise treatment. Biotechnol Adv 2023;68:108244. doi: 10.1016/j.biotechadv.2023.108244. (PMID: 10.1016/j.biotechadv.2023.108244)
Rovira M, Sereda R, Pladevall-Morera D, Ramponi V, Marin I, Maus M, et al. The lysosomal proteome of senescent cells contributes to the senescence secretome. Aging Cell 2022;21:e13707. doi: 10.1111/acel.13707. (PMID: 10.1111/acel.13707)
Nacarelli T, Sell C. Targeting metabolism in cellular senescence, a role for intervention. Mol Cell Endocrinol 2017;455:83-92. doi: 10.1016/j.mce.2016.08.049. (PMID: 10.1016/j.mce.2016.08.049)
Hernandez-Segura A, Nehme J, Demaria M. Hallmarks of cellular senescence. Trends Cell Biol 2018;28:436-453. doi: 10.1016/j.tcb.2018.02.001. (PMID: 10.1016/j.tcb.2018.02.001)
Yu B, Ma J, Li J, Wang D, Wang Z, Wang S. Mitochondrial phosphatase PGAM5 modulates cellular senescence by regulating mitochondrial dynamics. Nat Commun 2020;11:2549. doi: 10.1038/s41467-020-16312-7. (PMID: 10.1038/s41467-020-16312-7)
Park JT, Lee YS, Cho KA, Park SC. Adjustment of the lysosomal-mitochondrial axis for control of cellular senescence. Ageing Res Rev 2018;47:176-182. doi: 10.1016/j.arr.2018.08.003. (PMID: 10.1016/j.arr.2018.08.003)
Strycharz J, Drzewoski J, Szemraj J, Sliwinska A. Is p53 involved in tissue-specific insulin resistance formation? Oxid Med Cell Longev 2017;2017:9270549. doi: 10.1155/2017/9270549. (PMID: 10.1155/2017/9270549)
Li X, Chen M, Chen X, He X, Li X, Wei H, et al. TRAP1 drives smooth muscle cell senescence and promotes atherosclerosis via HDAC3-primed histone H4 lysine 12 lactylation. Eur Heart J 2024;45:4219-4235. doi: 10.1093/eurheartj/ehae379. (PMID: 10.1093/eurheartj/ehae379)
Liu L, Hao Z, Yang X, Li Y, Wang S, Li L. Metabolic reprogramming in T cell senescence: A novel strategy for cancer immunotherapy. Cell Death Discov 2025;11:161. doi: 10.1038/s41420-025-02468-y. (PMID: 10.1038/s41420-025-02468-y)
Wiley CD, Campisi J. The metabolic roots of senescence: Mechanisms and opportunities for intervention. Nat Metab 2021;3:1290-1301. doi: 10.1038/s42255-021-00483-8. (PMID: 10.1038/s42255-021-00483-8)
Liu B, Peng Z, Zhang H, Zhang N, Liu Z, Xia Z, et al. Regulation of cellular senescence in tumor progression and therapeutic targeting: Mechanisms and pathways. Mol Cancer 2025;24:106. doi: 10.1186/s12943-025-02284-z. (PMID: 10.1186/s12943-025-02284-z)
Felgentreff K, Baumann U, Klemann C, Schuetz C, Viemann D, Wetzke M, et al. Biomarkers of DNA damage response enable flow cytometry-based diagnostic to identify inborn DNA repair defects in primary immunodeficiencies. J Clin Immunol 2022;42:286-298. doi: 10.1007/s10875-021-01156-7. (PMID: 10.1007/s10875-021-01156-7)
Höhn A, Weber D, Jung T, Ott C, Hugo M, Kochlik B, et al. Happily (n)ever after: Aging in the context of oxidative stress, proteostasis loss and cellular senescence. Redox Biol 2017;11:482-501. doi: 10.1016/j.redox.2016.12.001. (PMID: 10.1016/j.redox.2016.12.001)
Myrianthopoulos V, Evangelou K, Vasileiou PVS, Cooks T, Vassilakopoulos TP, Pangalis GA, et al. Senescence and senotherapeutics: A new field in cancer therapy. Pharmacol Ther 2019;193:31-49. doi: 10.1016/j.pharmthera.2018.08.006. (PMID: 10.1016/j.pharmthera.2018.08.006)
Montague-Cardoso K. Cellular proteostasis decline in human senescence. Commun Biol 2021;4:17. doi: 10.1038/s42003-020-01578-w. (PMID: 10.1038/s42003-020-01578-w)
Ogrodnik M, Miwa S, Tchkonia T, Tiniakos D, Wilson CL, Lahat A, et al. Cellular senescence drives age-dependent hepatic steatosis. Nat Commun 2017;8:15691. doi: 10.1038/ncomms15691. (PMID: 10.1038/ncomms15691)
Haney MS, Pálovics R, Munson CN, Long C, Johansson PK, Yip O, et al. APOE4/4 is linked to damaging lipid droplets in Alzheimer’s disease microglia. Nature 2024;628:154-161. doi: 10.1038/s41586-024-07185-7. (PMID: 10.1038/s41586-024-07185-7)
Bailey AP, Koster G, Guillermier C, Hirst EMA, MacRae JI, Lechene CP, et al. Antioxidant role for lipid droplets in a stem cell niche of drosophila. Cell 2015;163:340-353. doi: 10.1016/j.cell.2015.09.020. (PMID: 10.1016/j.cell.2015.09.020)
Baar MP, Brandt RMC, Putavet DA, Klein JDD, Derks KWJ, Bourgeois BRM, et al. Targeted apoptosis of senescent cells restores tissue homeostasis in response to chemotoxicity and aging. Cell 2017;169:132-147.e16. doi: 10.1016/j.cell.2017.02.031. (PMID: 10.1016/j.cell.2017.02.031)
Yosef R, Pilpel N, Tokarsky-Amiel R, Biran A, Ovadya Y, Cohen S, et al. Directed elimination of senescent cells by inhibition of BCL-W and BCL-XL. Nature communications 2016;7. doi: 10.1038/ncomms11190. (PMID: 10.1038/ncomms11190)
Boise LH, González-García M, Postema CE, Ding L, Lindsten T, Turka LA, et al. Bcl-x, a bcl-2-related gene that functions as a dominant regulator of apoptotic cell death. Cell 1993;74:597-608. doi: 10.1016/0092-8674(93)90508-n. (PMID: 10.1016/0092-8674(93)90508-n)
Gadecka A, Nowak N, Bulanda E, Janiszewska D, Dudkowska M, Sikora E, et al. The senolytic cocktail, dasatinib and quercetin, impacts the chromatin structure of both young and senescent vascular smooth muscle cells. Geroscience 2025;47:3907-3925. doi: 10.1007/s11357-024-01504-6. (PMID: 10.1007/s11357-024-01504-6)
Rad AN, Grillari J. Current senolytics: Mode of action, efficacy and limitations, and their future. Mech Ageing Dev 2024;217:111888. doi: 10.1016/j.mad.2023.111888. (PMID: 10.1016/j.mad.2023.111888)
Liu Y, Hou Q, Wang R, Liu Y, Cheng Z. FOXO4-D-Retro-Inverso targets extracellular matrix production in fibroblasts and ameliorates bleomycin-induced pulmonary fibrosis in mice. Naunyn Schmiedebergs Arch Pharmacol 2023;396:2393-2403. doi: 10.1007/s00210-023-02452-2. (PMID: 10.1007/s00210-023-02452-2)
Xu X, Lou Z, Li J, Liang F, Yu Y, Wu M. Inhibition of Hsp90 alleviates necroptosis and inflammation in lung epithelial cells during pulmonary ischemia-reperfusion injury. Clin Exp Pharmacol Physiol 2025;52:e70037. doi: 10.1111/1440-1681.70037. (PMID: 10.1111/1440-1681.70037)
Agha-Mir-Salim D, Bhayadia R, Heckl D, Klusmann JH. Evaluation of Navitoclax (ABT-263) as a promising Therapy for Pediatric Acute Myeloid Leukemia. In: Klinische Pädiatrie, Vol 236. Georg Thieme Verlag KG; 2024:1.
Saliev T, Singh PB. Targeting Senescence: A review of senolytics and senomorphics in anti-aging interventions. Biomolecules 2025;15:860. doi: 10.3390/biom15060860. (PMID: 10.3390/biom15060860)
Amor C, Feucht J, Leibold J, Ho YJ, Zhu C, Alonso-Curbelo D, et al. Senolytic CAR T cells reverse senescence-associated pathologies. Nature 2020;583:127-132. doi: 10.1038/s41586-020-2403-9. (PMID: 10.1038/s41586-020-2403-9)
Ivanov A, Pawlikowski J, Manoharan I, van Tuyn J, Nelson DM, Rai TS, et al. Lysosome-mediated processing of chromatin in senescence. J Cell Biol 2013;202:129-143. doi: 10.1083/jcb.201212110. (PMID: 10.1083/jcb.201212110)
Bell O, Burton A, Dean C, Gasser SM, Torres-Padilla ME. Heterochromatin definition and function. Nat Rev Mol Cell Biol 2023;24:691-694. doi: 10.1038/s41580-023-00599-7. (PMID: 10.1038/s41580-023-00599-7)
Zhu X, Chen Z, Shen W, Huang G, Sedivy JM, Wang H, et al. Inflammation, epigenetics, and metabolism converge to cell senescence and ageing: The regulation and intervention. Signal Transduct Target Ther 2021;6:245. doi: 10.1038/s41392-021-00646-9. (PMID: 10.1038/s41392-021-00646-9)
Lee JH, Kim EW, Croteau DL, Bohr VA. Heterochromatin: An epigenetic point of view in aging. Exp Mol Med 2020;52:1466-1474. doi: 10.1038/s12276-020-00497-4. (PMID: 10.1038/s12276-020-00497-4)
Sati S, Bonev B, Szabo Q, Jost D, Bensadoun P, Serra F, et al. 4D genome rewiring during oncogene-induced and replicative senescence. Mol Cell 2020;78:522-538.e9. doi: 10.1016/j.molcel.2020.03.007. (PMID: 10.1016/j.molcel.2020.03.007)
Sharpless NE, Sherr CJ. Forging a signature of in vivo senescence. Nat Rev Cancer 2015;15:397-408. doi: 10.1038/nrc3960. (PMID: 10.1038/nrc3960)
Yao W, Hu X, Wang X. Crossing epigenetic frontiers: The intersection of novel histone modifications and diseases. Signal Transduct Target Ther 2024;9:232. doi: 10.1038/s41392-024-01918-w. (PMID: 10.1038/s41392-024-01918-w)
Wang Y, Yuan Q, Xie L. Histone modifications in aging: The underlying mechanisms and implications. Curr Stem Cell Res Ther 2018;13:125-135. doi: 10.2174/1574888X12666170817141921. (PMID: 10.2174/1574888X12666170817141921)
Willnow P, Teleman AA. Nuclear position and local acetyl-CoA production regulate chromatin state. Nature 2024;630:466-474. doi: 10.1038/s41586-024-07471-4. (PMID: 10.1038/s41586-024-07471-4)
Sahu RK, Dhakshnamoorthy J, Jain S, Folco HD, Wheeler D, Grewal S. Nucleosome remodeler exclusion by histone deacetylation enforces heterochromatic silencing and epigenetic inheritance. Mol Cell 2024;84:3175-3191.e8. doi: 10.1016/j.molcel.2024.07.006. (PMID: 10.1016/j.molcel.2024.07.006)
Di Giorgio E, Paluvai H, Dalla E, Ranzino L, Renzini A, Moresi V, et al. HDAC4 degradation during senescence unleashes an epigenetic program driven by AP-1/p300 at selected enhancers and super-enhancers. Genome Biol 2021;22:129. doi: 10.1186/s13059-021-02340-z. (PMID: 10.1186/s13059-021-02340-z)
Sen P, Lan Y, Li CY, Sidoli S, Donahue G, Dou Z, et al. Histone acetyltransferase p300 induces de novo super-enhancers to drive cellular senescence. Mol Cell 2019;73:684-698.e8. doi: 10.1016/j.molcel.2019.01.021. (PMID: 10.1016/j.molcel.2019.01.021)
Jambhekar A, Dhall A, Shi Y. Roles and regulation of histone methylation in animal development. Nat Rev Mol Cell Biol 2019;20:625-641. doi: 10.1038/s41580-019-0151-1. (PMID: 10.1038/s41580-019-0151-1)
Liu X, Liu Z, Wu Z, Ren J, Fan Y, Sun L, et al. Resurrection of endogenous retroviruses during aging reinforces senescence. Cell 2023;186:287-304.e26. doi: 10.1016/j.cell.2022.12.017. (PMID: 10.1016/j.cell.2022.12.017)
Ito T, Teo YV, Evans SA, Neretti N, Sedivy JM. Regulation of cellular senescence by polycomb chromatin modifiers through distinct DNA damage- and histone methylation-dependent pathways. Cell Rep 2018;22:3480-3492. doi: 10.1016/j.celrep.2018.03.002. (PMID: 10.1016/j.celrep.2018.03.002)
Barradas M, Anderton E, Acosta JC, Li S, Banito A, Rodriguez-Niedenführ M, et al. Histone demethylase JMJD3 contributes to epigenetic control of INK4a/ARF by oncogenic RAS. Genes Dev 2009;23:1177-1182. doi: 10.1101/gad.511109. (PMID: 10.1101/gad.511109)
Clapier CR, Cairns BR. The biology of chromatin remodeling complexes. Annu Rev Biochem 2009;78:273-304. doi: 10.1146/annurev.biochem.77.062706.153223. (PMID: 10.1146/annurev.biochem.77.062706.153223)
Liu Z, Ji Q, Ren J, Yan P, Wu Z, Wang S, et al. Large-scale chromatin reorganization reactivates placenta-specific genes that drive cellular aging. Dev Cell 2022;57:1347-1368.e12. doi: 10.1016/j.devcel.2022.05.004. (PMID: 10.1016/j.devcel.2022.05.004)
Jones MJ, Goodman SJ, Kobor MS. DNA methylation and healthy human aging. Aging Cell 2015;14:924-932. doi: 10.1111/acel.12349. (PMID: 10.1111/acel.12349)
Mauceri D. Role of epigenetic mechanisms in chronic pain. Cells 2022;11:2613. doi: 10.3390/cells11162613. (PMID: 10.3390/cells11162613)
Chandramouly G. Gadd45 in DNA demethylation and DNA repair. Adv Exp Med Biol 2022;1360:55-67. doi: 10.1007/978-3-030-94804-7_4. (PMID: 10.1007/978-3-030-94804-7_4)
Xu GL, Bochtler M. Reversal of nucleobase methylation by dioxygenases. Nat Chem Biol 2020;16:1160-1169. doi: 10.1038/s41589-020-00675-5. (PMID: 10.1038/s41589-020-00675-5)
Gulmez Karaca K, Brito DVC, Oliveira AMM. MeCP2: A critical regulator of chromatin in neurodevelopment and adult brain function. Int J Mol Sci 2019;20:4577. doi: 10.3390/ijms20184577. (PMID: 10.3390/ijms20184577)
Parry A, Rulands S, Reik W. Active turnover of DNA methylation during cell fate decisions. Nat Rev Genet 2021;22:59-66. doi: 10.1038/s41576-020-00287-8. (PMID: 10.1038/s41576-020-00287-8)
Baccarelli AA, Ordovás J. Epigenetics of early cardiometabolic disease: Mechanisms and precision medicine. Circ Res 2023;132:1648-1662. doi: 10.1161/CIRCRESAHA.123.322135. (PMID: 10.1161/CIRCRESAHA.123.322135)
Sakaki M, Ebihara Y, Okamura K, Nakabayashi K, Igarashi A, Matsumoto K, et al. Potential roles of DNA methylation in the initiation and establishment of replicative senescence revealed by array-based methylome and transcriptome analyses. PLoS One 2017;12:e0171431. doi: 10.1371/journal.pone.0171431. (PMID: 10.1371/journal.pone.0171431)
Zhu B, Gong Y, Yan G, Wang D, Wang Q, Qiao Y, et al. Atorvastatin treatment modulates p16 promoter methylation to regulate p16 expression. FEBS J 2017;284:1868-1881. doi: 10.1111/febs.14087. (PMID: 10.1111/febs.14087)
Fan Y, Lv X, Chen Z, Peng Y, Zhang M. m6A methylation: Critical roles in aging and neurological diseases. Front Mol Neurosci 2023;16:1102147. doi: 10.3389/fnmol.2023.1102147. (PMID: 10.3389/fnmol.2023.1102147)
Gao P, Yao F, Pang J, Yin K, Zhu X. m 6A methylation in cellular senescence of age-associated diseases. Acta Biochim Biophys Sin (Shanghai) 2023;55:1168-1183. doi: 10.3724/abbs.2023107. (PMID: 10.3724/abbs.2023107)
Wagner A, Schosserer M. The epitranscriptome in ageing and stress resistance: A systematic review. Ageing Res Rev 2022;81:101700. doi: 10.1016/j.arr.2022.101700. (PMID: 10.1016/j.arr.2022.101700)
Chen LL, Kim VN. Small and long non-coding RNAs: Past, present, and future. Cell 2024;187:6451-6485. doi: 10.1016/j.cell.2024.10.024. (PMID: 10.1016/j.cell.2024.10.024)
Potter ML, Hill WD, Isales CM, Hamrick MW, Fulzele S. MicroRNAs are critical regulators of senescence and aging in mesenchymal stem cells. Bone 2021;142:115679. doi: 10.1016/j.bone.2020.115679. (PMID: 10.1016/j.bone.2020.115679)
Ferrer J, Dimitrova N. Transcription regulation by long non-coding RNAs: Mechanisms and disease relevance. Nat Rev Mol Cell Biol 2024;25:396-415. doi: 10.1038/s41580-023-00694-9. (PMID: 10.1038/s41580-023-00694-9)
Hu C, Zhang X, Teng T, Ma ZG, Tang QZ. Cellular senescence in cardiovascular diseases: A systematic review. Aging Dis 2022;13:103-128. doi: 10.14336/AD.2021.0927. (PMID: 10.14336/AD.2021.0927)
Johmura Y, Yamanaka T, Omori S, Wang TW, Sugiura Y, Matsumoto M, et al. Senolysis by glutaminolysis inhibition ameliorates various age-associated disorders. Science 2021;371:265-270. doi: 10.1126/science.abb5916. (PMID: 10.1126/science.abb5916)
You Y, Chen X, Chen Y, Pang J, Chen Q, Liu Q, et al. Epigenetic modulation of Drp1-mediated mitochondrial fission by inhibition of S-adenosylhomocysteine hydrolase promotes vascular senescence and atherosclerosis. Redox Biol 2023;65:102828. doi: 10.1016/j.redox.2023.102828. (PMID: 10.1016/j.redox.2023.102828)
Stojanović SD, Fiedler J, Bauersachs J, Thum T, Sedding DG. Senescence-induced inflammation: An important player and key therapeutic target in atherosclerosis. Eur Heart J 2020;41:2983-2996. doi: 10.1093/eurheartj/ehz919. (PMID: 10.1093/eurheartj/ehz919)
Borén J, Chapman MJ, Krauss RM, Packard CJ, Bentzon JF, Binder CJ, et al. Low-density lipoproteins cause atherosclerotic cardiovascular disease: Pathophysiological, genetic, and therapeutic insights: a consensus statement from the European Atherosclerosis Society Consensus Panel. Eur Heart J 2020;41:2313-2330. doi: 10.1093/eurheartj/ehz962. (PMID: 10.1093/eurheartj/ehz962)
Childs BG, Baker DJ, Wijshake T, Conover CA, Campisi J, van Deursen JM. Senescent intimal foam cells are deleterious at all stages of atherosclerosis. Science 2016;354:472-477. doi: 10.1126/science.aaf6659. (PMID: 10.1126/science.aaf6659)
Aschacher T, Geisler D, Lenz V, Aschacher O, Winkler B, Schaefer AK, et al. Impacts of telomeric length, chronic hypoxia, senescence, and senescence-associated secretory phenotype on the development of thoracic aortic aneurysm. Int J Mol Sci 2022;23:15498. doi: 10.3390/ijms232415498. (PMID: 10.3390/ijms232415498)
Chen MS, Lee RT, Garbern JC. Senescence mechanisms and targets in the heart. Cardiovasc Res 2022;118:1173-1187. doi: 10.1093/cvr/cvab161. (PMID: 10.1093/cvr/cvab161)
Bloom SI, Islam MT, Lesniewski LA, Donato AJ. Mechanisms and consequences of endothelial cell senescence. Nat Rev Cardiol 2023;20:38-51. doi: 10.1038/s41569-022-00739-0. (PMID: 10.1038/s41569-022-00739-0)
Grootaert MOJ, Finigan A, Figg NL, Uryga AK, Bennett MR. SIRT6 protects smooth muscle cells from senescence and reduces atherosclerosis. Circ Res 2021;128:474-491. doi: 10.1161/CIRCRESAHA.120.318353. (PMID: 10.1161/CIRCRESAHA.120.318353)
Jaiswal S, Natarajan P, Silver AJ, Gibson CJ, Bick AG, Shvartz E, et al. Clonal hematopoiesis and risk of atherosclerotic cardiovascular disease. N Engl J Med 2017;377:111-121. doi: 10.1056/NEJMoa1701719. (PMID: 10.1056/NEJMoa1701719)
Sano S, Oshima K, Wang Y, Katanasaka Y, Sano M, Walsh K. CRISPR-mediated gene editing to assess the roles of Tet2 and Dnmt3a in clonal hematopoiesis and cardiovascular disease. Circ Res 2018;123:335-341. doi: 10.1161/CIRCRESAHA.118.313225. (PMID: 10.1161/CIRCRESAHA.118.313225)
Libby P. The changing landscape of atherosclerosis. Nature 2021;592:524-533. doi: 10.1038/s41586-021-03392-8. (PMID: 10.1038/s41586-021-03392-8)
Childs BG, Zhang C, Shuja F, Sturmlechner I, Trewartha S, Fierro Velasco R, et al. Senescent cells suppress innate smooth muscle cell repair functions in atherosclerosis. Nat Aging 2021;1:698-714. doi: 10.1038/s43587-021-00089-5. (PMID: 10.1038/s43587-021-00089-5)
Karnewar S, Karnewar V, Shankman LS, Owens GK. Treatment of advanced atherosclerotic mice with ABT-263 reduced indices of plaque stability and increased mortality. JCI Insight 2024;9:e173863. doi: 10.1172/jci.insight.173863. (PMID: 10.1172/jci.insight.173863)
Tang X, Li PH, Chen HZ. Cardiomyocyte senescence and cellular communications within myocardial microenvironments. Front Endocrinol (Lausanne) 2020;11:280. doi: 10.3389/fendo.2020.00280. (PMID: 10.3389/fendo.2020.00280)
El-Nachef D, Oyama K, Wu YY, Freeman M, Zhang Y, MacLellan WR. Repressive histone methylation regulates cardiac myocyte cell cycle exit. J Mol Cell Cardiol 2018;121:1-12. doi: 10.1016/j.yjmcc.2018.05.013. (PMID: 10.1016/j.yjmcc.2018.05.013)
Saito Y, Yamamoto S, Chikenji TS. Role of cellular senescence in inflammation and regeneration. Inflamm Regen 2024;44:28. doi: 10.1186/s41232-024-00342-5. (PMID: 10.1186/s41232-024-00342-5)
Liu M, Yu Z, He Z, Zhou Z, Liu J, Liu L, et al. Blocking nuclear receptor Nr4a3 unlocks the senescence barrier to promote direct cardiac reprogramming. Sci Adv 2025;11:eadz4847. doi: 10.1126/sciadv.adz4847. (PMID: 10.1126/sciadv.adz4847)
Xu P, Wang M, Song WM, Wang Q, Yuan GC, Sudmant PH, et al. The landscape of human tissue and cell type specific expression and co-regulation of senescence genes. Mol Neurodegener 2022;17:5. doi: 10.1186/s13024-021-00507-7. (PMID: 10.1186/s13024-021-00507-7)
de Mera-Rodríguez JA, Álvarez-Hernán G, Gañán Y, Santos-Almeida A, Martín-Partido G, Rodríguez-León J, et al. Endogenous pH 6.0 β-galactosidase activity is linked to neuronal differentiation in the olfactory epithelium. Cells 2022;11:298. doi: 10.3390/cells11020298. (PMID: 10.3390/cells11020298)
Chou SM, Yen YH, Yuan F, Zhang SC, Chong CM. Neuronal senescence in the aged brain. Aging Dis 2023;14:1618-1632. doi: 10.14336/AD.2023.0214. (PMID: 10.14336/AD.2023.0214)
Ristori S, Bertoni G, Bientinesi E, Monti D. The role of nutraceuticals and functional foods in mitigating cellular senescence and its related aspects: A key strategy for delaying or preventing aging and neurodegenerative disorders. Nutrients 2025;17:1837. doi: 10.3390/nu17111837. (PMID: 10.3390/nu17111837)
Liddelow SA, Olsen ML, Sofroniew MV. Reactive astrocytes and emerging roles in central nervous system (CNS) disorders. Cold Spring Harb Perspect Biol 2024;16:a041356. doi: 10.1101/cshperspect.a041356. (PMID: 10.1101/cshperspect.a041356)
Dehkordi SK, Walker J, Sah E, Bennett E, Atrian F, Frost B, et al. Profiling senescent cells in human brains reveals neurons with CDKN2D/p19 and tau neuropathology. Nat Aging 2021;1:1107-1116. doi: 10.1038/s43587-021-00142-3. (PMID: 10.1038/s43587-021-00142-3)
Moh C, Kubiak JZ, Bajic VP, Zhu X, Smith MA, Lee HG. Cell cycle deregulation in the neurons of Alzheimer’s disease. Results Probl Cell Differ 2011;53:565-576. doi: 10.1007/978-3-642-19065-0_23. (PMID: 10.1007/978-3-642-19065-0_23)
Wu D, Sun JKL, Chow KHM. Neuronal cell cycle reentry events in the aging brain are more prevalent in neurodegeneration and lead to cellular senescence. PLoS Biol 2024;22:e3002559. doi: 10.1371/journal.pbio.3002559. (PMID: 10.1371/journal.pbio.3002559)
Ng PY, Zhang C, Li H, Baker DJ. Senescent microglia represent a subset of disease-associated microglia in P301S mice. J Alzheimers Dis 2023;95:493-507. doi: 10.3233/JAD-230109. (PMID: 10.3233/JAD-230109)
Ungerleider K, Beck JA, Lissa D, Joruiz S, Horikawa I, Harris CC. Δ133p53α protects human astrocytes from amyloid-beta induced senescence and neurotoxicity. Neuroscience 2022;498:190-202. doi: 10.1016/j.neuroscience.2022.06.004. (PMID: 10.1016/j.neuroscience.2022.06.004)
Huang Y, Liu B, Sinha SC, Amin S, Gan L. Mechanism and therapeutic potential of targeting cGAS-STING signaling in neurological disorders. Mol Neurodegener 2023;18:79. doi: 10.1186/s13024-023-00672-x. (PMID: 10.1186/s13024-023-00672-x)
Heneka MT, Kummer MP, Latz E. Innate immune activation in neurodegenerative disease. Nat Rev Immunol 2014;14:463-477. doi: 10.1038/nri3705. (PMID: 10.1038/nri3705)
Bae EJ, Choi M, Kim JT, Kim DK, Jung MK, Kim C, et al. TNF-α promotes α-synuclein propagation through stimulation of senescence-associated lysosomal exocytosis. Exp Mol Med 2022;54:788-800. doi: 10.1038/s12276-022-00789-x. (PMID: 10.1038/s12276-022-00789-x)
Russo T, Kolisnyk B, B S A, Plessis-Belair J, Kim TW, Martin J, et al. The SATB1-MIR22-GBA axis mediates glucocerebroside accumulation inducing a cellular senescence-like phenotype in dopaminergic neurons. Aging Cell 2024;23:e14077. doi: 10.1111/acel.14077. (PMID: 10.1111/acel.14077)
Jiang Q, Liu J, Huang S, Wang XY, Chen X, Liu GH, et al. Antiageing strategy for neurodegenerative diseases: From mechanisms to clinical advances. Signal Transduct Target Ther 2025;10:76. doi: 10.1038/s41392-025-02145-7. (PMID: 10.1038/s41392-025-02145-7)
Bellelli F, Angioni D, Arosio B, Vellas B, De Souto Barreto P. Hallmarks of aging and Alzheimer’s disease pathogenesis: Paving the route for new therapeutic targets. Ageing Res Rev 2025;106:102699. doi: 10.1016/j.arr.2025.102699. (PMID: 10.1016/j.arr.2025.102699)
Basova LV, Bortell N, Conti B, Fox HS, Milner R, Marcondes MCG. Age-associated changes in microglia activation and Sirtuin-1- chromatin binding patterns. Aging (Albany NY) 2022;14:8205-8220. doi: 10.18632/aging.204329. (PMID: 10.18632/aging.204329)
Nativio R, Lan Y, Donahue G, Sidoli S, Berson A, Srinivasan AR, et al. An integrated multi-omics approach identifies epigenetic alterations associated with Alzheimer’s disease. Nat Genet 2020;52:1024-1035. doi: 10.1038/s41588-020-0696-0. (PMID: 10.1038/s41588-020-0696-0)
Peleg S, Sananbenesi F, Zovoilis A, Burkhardt S, Bahari-Javan S, Agis-Balboa RC, et al. Altered histone acetylation is associated with age-dependent memory impairment in mice. Science 2010;328:753-756. doi: 10.1126/science.1186088. (PMID: 10.1126/science.1186088)
Min SW, Chen X, Tracy TE, Li Y, Zhou Y, Wang C, et al. Critical role of acetylation in tau-mediated neurodegeneration and cognitive deficits. Nat Med 2015;21:1154-1162. doi: 10.1038/nm.3951. (PMID: 10.1038/nm.3951)
Karabag D, Heneka MT, Ising C. The putative contribution of cellular senescence to driving tauopathies. Trends Immunol 2024;45:837-848. doi: 10.1016/j.it.2024.08.006. (PMID: 10.1016/j.it.2024.08.006)
Lytrivi M, Castell AL, Poitout V, Cnop M. Recent insights into mechanisms of β-cell lipo- and glucolipotoxicity in type 2 diabetes. J Mol Biol 2020;432:1514-1534. doi: 10.1016/j.jmb.2019.09.016. (PMID: 10.1016/j.jmb.2019.09.016)
Avrahami D, Li C, Zhang J, Schug J, Avrahami R, Rao S, et al. Aging-dependent demethylation of regulatory elements correlates with chromatin state and improved β cell function. Cell Metab 2015;22:619-632. doi: 10.1016/j.cmet.2015.07.025. (PMID: 10.1016/j.cmet.2015.07.025)
De Jesus DF, Zhang Z, Kahraman S, Brown NK, Chen M, Hu J, et al. m6A mRNA methylation regulates human β-cell biology in physiological states and in type 2 diabetes. Nat Metab 2019;1:765-774. doi: 10.1038/s42255-019-0089-9. (PMID: 10.1038/s42255-019-0089-9)
Wilinski D, Dus M. N6-adenosine methylation controls the translation of insulin mRNA. Nat Struct Mol Biol 2023;30:1260-1264. doi: 10.1038/s41594-023-01048-x. (PMID: 10.1038/s41594-023-01048-x)
Callender LA, Carroll EC, Garrod-Ketchley C, Schroth J, Bystrom J, Berryman V, et al. Altered nutrient uptake causes mitochondrial dysfunction in senescent CD8+ EMRA T cells during type 2 diabetes. Front Aging 2021;2:681428. doi: 10.3389/fragi.2021.681428. (PMID: 10.3389/fragi.2021.681428)
Lee YH, Kim SR, Han DH, Yu HT, Han YD, Kim JH, et al. Senescent T cells predict the development of hyperglycemia in humans. Diabetes 2019;68:156-162. doi: 10.2337/db17-1218. (PMID: 10.2337/db17-1218)
Yi HS, Kim SY, Kim JT, Lee YS, Moon JS, Kim M, et al. T-cell senescence contributes to abnormal glucose homeostasis in humans and mice. Cell Death Dis 2019;10:249. doi: 10.1038/s41419-019-1494-4. (PMID: 10.1038/s41419-019-1494-4)
Guo C, Li X, Fan Z, Zhang J, Chen M. Progress in the study of the role of C5a-induced tubular cell senescence in the progression of diabetic kidney disease. Ann Med 2025;57:2561232. doi: 10.1080/07853890.2025.2561232. (PMID: 10.1080/07853890.2025.2561232)
Liebisch M, Wolf G. AGE-induced suppression of EZH2 mediates injury of podocytes by reducing H3K27me3. Am J Nephrol 2020;51:676-692. doi: 10.1159/000510140. (PMID: 10.1159/000510140)
Chen J, He J, Wang X, Bai L, Yang X, Chen J, et al. Glis1 inhibits RTEC cellular senescence and renal fibrosis by downregulating histone lactylation in DKD. Life Sci 2025;361:123293. doi: 10.1016/j.lfs.2024.123293. (PMID: 10.1016/j.lfs.2024.123293)
Pouw RB, Ricklin D. Tipping the balance: Intricate roles of the complement system in disease and therapy. Semin Immunopathol 2021;43:757-771. doi: 10.1007/s00281-021-00892-7. (PMID: 10.1007/s00281-021-00892-7)
Palmer AK, Xu M, Zhu Y, Pirtskhalava T, Weivoda MM, Hachfeld CM, et al. Targeting senescent cells alleviates obesity-induced metabolic dysfunction. Aging Cell 2019;18:e12950. doi: 10.1111/acel.12950. (PMID: 10.1111/acel.12950)
Prattichizzo F, de Candia P, Ceriello A. Diabetes and kidney disease: Emphasis on treatment with SGLT-2 inhibitors and GLP-1 receptor agonists. Metabolism 2021;120:154799. doi: 10.1016/j.metabol.2021.154799. (PMID: 10.1016/j.metabol.2021.154799)
Al-Dabet MM, Shahzad K, Elwakiel A, Sulaj A, Kopf S, Bock F, et al. Reversal of the renal hyperglycemic memory in diabetic kidney disease by targeting sustained tubular p21 expression. Nat Commun 2022;13:5062. doi: 10.1038/s41467-022-32477-9. (PMID: 10.1038/s41467-022-32477-9)
Natarajan R. Epigenetic mechanisms in diabetic vascular complications and metabolic memory: The 2020 Edwin Bierman Award Lecture. Diabetes 2021;70:328-337. doi: 10.2337/dbi20-0030. (PMID: 10.2337/dbi20-0030)
Nebbioso M, Lambiase A, Armentano M, Tucciarone G, Sacchetti M, Greco A, et al. Diabetic retinopathy, oxidative stress, and sirtuins: An in depth look in enzymatic patterns and new therapeutic horizons. Surv Ophthalmol 2022;67:168-183. doi: 10.1016/j.survophthal.2021.04.003. (PMID: 10.1016/j.survophthal.2021.04.003)
Kim Y, Kang M, Mamo MG, Adisasmita M, Huch M, Choi D. Liver organoids: Current advances and future applications for hepatology. Clin Mol Hepatol 2025;31:S327-S348. doi: 10.3350/cmh.2024.1040. (PMID: 10.3350/cmh.2024.1040)
Ramanathan R, Ali AH, Ibdah JA. Mitochondrial dysfunction plays central role in nonalcoholic fatty liver disease. Int J Mol Sci 2022;23:7280. doi: 10.3390/ijms23137280. (PMID: 10.3390/ijms23137280)
Dabravolski SA, Bezsonov EE, Orekhov AN. The role of mitochondria dysfunction and hepatic senescence in NAFLD development and progression. Biomed Pharmacother 2021;142:112041. doi: 10.1016/j.biopha.2021.112041. (PMID: 10.1016/j.biopha.2021.112041)
Chen J, Li G, He X, Chen X, Chen Z, Liu D, et al. ELMO1 ameliorates intestinal epithelial cellular senescence via SIRT1/p65 signaling in inflammatory bowel disease-related fibrosis. Gastroenterol Rep (Oxf) 2024;12:goae045. doi: 10.1093/gastro/goae045. (PMID: 10.1093/gastro/goae045)
Zhang CY, Tan XH, Yang HH, Jin L, Hong JR, Zhou Y, et al. COX-2/sEH dual inhibitor alleviates hepatocyte senescence in NAFLD mice by restoring autophagy through Sirt1/PI3K/AKT/mTOR. Int J Mol Sci 2022;23:8267. doi: 10.3390/ijms23158267. (PMID: 10.3390/ijms23158267)
Kaji K, Factor VM, Andersen JB, Durkin ME, Tomokuni A, Marquardt JU, et al. DNMT1 is a required genomic regulator for murine liver histogenesis and regeneration. Hepatology 2016;64:582-598. doi: 10.1002/hep.28563. (PMID: 10.1002/hep.28563)
Palma R, Pronio A, Romeo M, Scognamiglio F, Ventriglia L, Ormando VM, et al. The role of insulin resistance in fueling NAFLD pathogenesis: From molecular mechanisms to clinical implications. J Clin Med 2022;11:3649. doi: 10.3390/jcm11133649. (PMID: 10.3390/jcm11133649)
Barazzoni R, Gortan Cappellari G, Ragni M, Nisoli E. Insulin resistance in obesity: An overview of fundamental alterations. Eat Weight Disord 2018;23:149-157. doi: 10.1007/s40519-018-0481-6. (PMID: 10.1007/s40519-018-0481-6)
Zhao M, Wang L, Wang M, Zhou S, Lu Y, Cui H, et al. Targeting fibrosis, mechanisms and cilinical trials. Signal Transduct Target Ther 2022;7:206. doi: 10.1038/s41392-022-01070-3. (PMID: 10.1038/s41392-022-01070-3)
Yamashita N, Kramann R. Mechanisms of kidney fibrosis and routes towards therapy. Trends Endocrinol Metab 2024;35:31-48. doi: 10.1016/j.tem.2023.09.001. (PMID: 10.1016/j.tem.2023.09.001)
DePianto DJ, Heiden J, Morshead KB, Sun KH, Modrusan Z, Teng G, et al. Molecular mapping of interstitial lung disease reveals a phenotypically distinct senescent basal epithelial cell population. JCI Insight 2021;6:e143626. doi: 10.1172/jci.insight.143626. (PMID: 10.1172/jci.insight.143626)
Tian Y, Li H, Qiu T, Dai J, Zhang Y, Chen J, et al. Loss of PTEN induces lung fibrosis via alveolar epithelial cell senescence depending on NF-κB activation. Aging Cell 2019;18:e12858. doi: 10.1111/acel.12858. (PMID: 10.1111/acel.12858)
Lehmann M, Korfei M, Mutze K, Klee S, Skronska-Wasek W, Alsafadi HN, et al. Senolytic drugs target alveolar epithelial cell function and attenuate experimental lung fibrosis ex vivo . Eur Respir J 2017;50:1602367. doi: 10.1183/13993003.02367-2016. (PMID: 10.1183/13993003.02367-2016)
Schafer MJ, White TA, Iijima K, Haak AJ, Ligresti G, Atkinson EJ, et al. Cellular senescence mediates fibrotic pulmonary disease. Nat Commun 2017;8:14532. doi: 10.1038/ncomms14532. (PMID: 10.1038/ncomms14532)
Hohmann MS, Habiel DM, Coelho AL, Verri WA, Hogaboam CM. Quercetin enhances ligand-induced apoptosis in senescent idiopathic pulmonary fibrosis fibroblasts and reduces lung fibrosis in vivo . Am J Respir Cell Mol Biol 2019;60:28-40. doi: 10.1165/rcmb.2017-0289OC. (PMID: 10.1165/rcmb.2017-0289OC)
Cui H, Ge J, Xie N, Banerjee S, Zhou Y, Antony VB, et al. miR-34a inhibits lung fibrosis by inducing lung fibroblast senescence. Am J Respir Cell Mol Biol 2017;56:168-178. doi: 10.1165/rcmb.2016-0163OC. (PMID: 10.1165/rcmb.2016-0163OC)
Zhu Y, Anastasiadis ZP, Espindola Netto JM, Evans T, Tchkonia T, et al. Past and future directions for research on cellular senescence. Cold Spring Harb Perspect Med 2024;14:a041205. doi: 10.1101/cshperspect.a041205. (PMID: 10.1101/cshperspect.a041205)
Vats A, Chaturvedi P. The Regenerative power of stem cells: Treating bleomycin-induced lung fibrosis. Stem Cells Cloning 2023;16:43-59. doi: 10.2147/SCCAA.S419474. (PMID: 10.2147/SCCAA.S419474)
Shi L, Han Q, Hong Y, Li W, Gong G, Cui J, et al. Inhibition of miR-199a-5p rejuvenates aged mesenchymal stem cells derived from patients with idiopathic pulmonary fibrosis and improves their therapeutic efficacy in experimental pulmonary fibrosis. Stem Cell Res Ther 2021;12:147. doi: 10.1186/s13287-021-02215-x. (PMID: 10.1186/s13287-021-02215-x)
Zhou J, Chen H, Wang Q, Chen S, Wang R, Wang Z, et al. Sirt1 overexpression improves senescence-associated pulmonary fibrosis induced by vitamin D deficiency through downregulating IL-11 transcription. Aging Cell 2022;21:e13680. doi: 10.1111/acel.13680. (PMID: 10.1111/acel.13680)
Tilman G, Bouzin C, Aydin S, Tamirou F, Galant C, Coulie PG, et al. High p16INK4a, a marker of cellular senescence, is associated with renal injury, impairment and outcome in lupus nephritis. RMD Open 2021;7:e001844. doi: 10.1136/rmdopen-2021-001844. (PMID: 10.1136/rmdopen-2021-001844)
Gong W, Luo C, Peng F, Xiao J, Zeng Y, Yin B, et al. Brahma-related gene-1 promotes tubular senescence and renal fibrosis through Wnt/β-catenin/autophagy axis. Clin Sci (Lond) 2021;135:1873-1895. doi: 10.1042/CS20210447. (PMID: 10.1042/CS20210447)
Li S, Livingston MJ, Ma Z, Hu X, Wen L, Ding HF, et al. Tubular cell senescence promotes maladaptive kidney repair and chronic kidney disease after cisplatin nephrotoxicity. JCI Insight 2023;8:e166643. doi: 10.1172/jci.insight.166643. (PMID: 10.1172/jci.insight.166643)
Zhang JQ, Li YY, Zhang XY, Tian ZH, Liu C, Wang ST, et al. Cellular senescence of renal tubular epithelial cells in renal fibrosis. Front Endocrinol (Lausanne) 2023;14:1085605. doi: 10.3389/fendo.2023.1085605. (PMID: 10.3389/fendo.2023.1085605)
Bao Y, Shan Q, Lu K, Yang Q, Liang Y, Kuang H, et al. Renal tubular epithelial cell quality control mechanisms as therapeutic targets in renal fibrosis. J Pharm Anal 2024;14:100933. doi: 10.1016/j.jpha.2024.01.001. (PMID: 10.1016/j.jpha.2024.01.001)
Schunk SJ, Floege J, Fliser D, Speer T. WNT-β-catenin signalling-a versatile player in kidney injury and repair. Nat Rev Nephrol 2021;17:172-184. doi: 10.1038/s41581-020-00343-w. (PMID: 10.1038/s41581-020-00343-w)
Hassan N, Shehatou G, Kenawy HI, Said E. Dasatinib mitigates renal fibrosis in a rat model of UUO via inhibition of Src/STAT-3/NF-κB signaling. Environ Toxicol Pharmacol 2021;84:103625. doi: 10.1016/j.etap.2021.103625. (PMID: 10.1016/j.etap.2021.103625)
Castellano G, Franzin R, Sallustio F, Stasi A, Banelli B, Romani M, et al. Complement component C5a induces aberrant epigenetic modifications in renal tubular epithelial cells accelerating senescence by Wnt4/βcatenin signaling after ischemia/reperfusion injury. Aging (Albany NY) 2019;11:4382-4406. doi: 10.18632/aging.102059. (PMID: 10.18632/aging.102059)
Yin Q, Tang TT, Lu XY, Ni WJ, Yin D, Zhang YL, et al. Macrophage-derived exosomes promote telomere fragility and senescence in tubular epithelial cells by delivering miR-155. Cell Commun Signal 2024;22:357. doi: 10.1186/s12964-024-01708-5. (PMID: 10.1186/s12964-024-01708-5)
Pan C, Wang X, Fan Z, Mao W, Shi Y, Wu Y, et al. Polystyrene microplastics facilitate renal fibrosis through accelerating tubular epithelial cell senescence. Food Chem Toxicol 2024;191:114888. doi: 10.1016/j.fct.2024.114888. (PMID: 10.1016/j.fct.2024.114888)
Zhang XT, Wang G, Ye LF, Pu Y, Li RT, Liang J, et al. Baicalin reversal of DNA hypermethylation-associated Klotho suppression ameliorates renal injury in type 1 diabetic mouse model. Cell Cycle 2020;19:3329-3347. doi: 10.1080/15384101.2020.1843815. (PMID: 10.1080/15384101.2020.1843815)
Zhang X, Li L, Tan H, Hong X, Yuan Q, Hou FF, et al. Klotho-derived peptide 1 inhibits cellular senescence in the fibrotic kidney by restoring Klotho expression via posttranscriptional regulation. Theranostics 2024;14:420-435. doi: 10.7150/thno.89105. (PMID: 10.7150/thno.89105)
Kim H, Yu MR, Lee H, Kwon SH, Jeon JS, Han DC, et al. Metformin inhibits chronic kidney disease-induced DNA damage and senescence of mesenchymal stem cells. Aging Cell 2021;20:e13317. doi: 10.1111/acel.13317. (PMID: 10.1111/acel.13317)
Wang Y, Wang Y, Yang M, Ma X. Implication of cellular senescence in the progression of chronic kidney disease and the treatment potencies. Biomed Pharmacother 2021;135:111191. doi: 10.1016/j.biopha.2020.111191. (PMID: 10.1016/j.biopha.2020.111191)
Zhang Y, Gong C, Tao L, Zhai J, Huang F, Zhang S. Involvement of SIRT1-mediated aging in liver diseases. Front Cell Dev Biol 2025;13:1548015. doi: 10.3389/fcell.2025.1548015. (PMID: 10.3389/fcell.2025.1548015)
Kamm DR, McCommis KS. Hepatic stellate cells in physiology and pathology. J Physiol 2022;600:1825-1837. doi: 10.1113/JP281061. (PMID: 10.1113/JP281061)
Zhang M, Serna-Salas S, Damba T, Borghesan M, Demaria M, Moshage H. Hepatic stellate cell senescence in liver fibrosis: Characteristics, mechanisms and perspectives. Mechanisms of Ageing and Development 2021;199:111572. doi: 10.1016/j.mad.2021.111572. (PMID: 10.1016/j.mad.2021.111572)
Lujambio A, Akkari L, Simon J, Grace D, Tschaharganeh DF, Bolden JE, et al. Non-cell-autonomous tumor suppression by p53. Cell 2013;153:449-460. doi: 10.1016/j.cell.2013.03.020. (PMID: 10.1016/j.cell.2013.03.020)
Jiang Y, Xiang C, Zhong F, Zhang Y, Wang L, Zhao Y, et al. Histone H3K27 methyltransferase EZH2 and demethylase JMJD3 regulate hepatic stellate cells activation and liver fibrosis. Theranostics 2021;11:361-378. doi: 10.7150/thno.46360. (PMID: 10.7150/thno.46360)
Chen L, Liang B, Xia S, Wang F, Li Z, Shao J, et al. Emodin promotes hepatic stellate cell senescence and alleviates liver fibrosis via a nuclear receptor (Nur77)-mediated epigenetic regulation of glutaminase 1. Br J Pharmacol 2023;180:2577-2598. doi: 10.1111/bph.16156. (PMID: 10.1111/bph.16156)
Selman M, López-Otín C, Pardo A. Age-driven developmental drift in the pathogenesis of idiopathic pulmonary fibrosis. Eur Respir J 2016;48:538-552. doi: 10.1183/13993003.00398-2016. (PMID: 10.1183/13993003.00398-2016)
Yao C, Guan X, Carraro G, Parimon T, Liu X, Huang G, et al. Senescence of alveolar type 2 cells drives progressive pulmonary fibrosis. Am J Respir Crit Care Med 2021;203:707-717. doi: 10.1164/rccm.202004-1274OC. (PMID: 10.1164/rccm.202004-1274OC)
Colucci M, Sarill M, Maddalena M, Valdata A, Troiani M, Massarotti M, et al. Senescence in cancer. Cancer Cell 2025;43:1204-1226. doi: 10.1016/j.ccell.2025.05.015. (PMID: 10.1016/j.ccell.2025.05.015)
Kolodkin-Gal D, Roitman L, Ovadya Y, Azazmeh N, Assouline B, Schlesinger Y, et al. Senolytic elimination of Cox2-expressing senescent cells inhibits the growth of premalignant pancreatic lesions. Gut 2022;71:345-355. doi: 10.1136/gutjnl-2020-321112. (PMID: 10.1136/gutjnl-2020-321112)
Schmitt CA, Wang B, Demaria M. Senescence and cancer-role and therapeutic opportunities. Nat Rev Clin Oncol 2022;19:619-636. doi: 10.1038/s41571-022-00668-4. (PMID: 10.1038/s41571-022-00668-4)
Yamamoto K, Tateishi K, Kudo Y, Sato T, Yamamoto S, Miyabayashi K, et al. Loss of histone demethylase KDM6B enhances aggressiveness of pancreatic cancer through downregulation of C/EBPα. Carcinogenesis 2014;35:2404-2414. doi: 10.1093/carcin/bgu136. (PMID: 10.1093/carcin/bgu136)
Kaneko S, Li X. X chromosome protects against bladder cancer in females via a KDM6A-dependent epigenetic mechanism. Sci Adv 2018;4:eaar5598. doi: 10.1126/sciadv.aar5598. (PMID: 10.1126/sciadv.aar5598)
Chibaya L, Murphy KC, DeMarco KD, Gopalan S, Liu H, Parikh CN, et al. EZH2 inhibition remodels the inflammatory senescence-associated secretory phenotype to potentiate pancreatic cancer immune surveillance. Nat Cancer 2023;4:872-892. doi: 10.1038/s43018-023-00553-8. (PMID: 10.1038/s43018-023-00553-8)
Ruscetti M, Leibold J, Bott MJ, Fennell M, Kulick A, Salgado NR, et al. NK cell-mediated cytotoxicity contributes to tumor control by a cytostatic drug combination. Science 2018;362:1416-1422. doi: 10.1126/science.aas9090. (PMID: 10.1126/science.aas9090)
Li L, Hao S, Gao M, Liu J, Xu X, Huang J, et al. HDAC3 inhibition promotes antitumor immunity by enhancing CXCL10-mediated chemotaxis and recruiting of immune cells. Cancer Immunol Res 2023;11:657-673. doi: 10.1158/2326-6066.CIR-22-0317. (PMID: 10.1158/2326-6066.CIR-22-0317)
Zhang X, Li P, Gan Y, Xiang S, Gu L, Zhou J, et al. Driving effect of P16 methylation on telomerase reverse transcriptase-mediated immortalization and transformation of normal human fibroblasts. Chin Med J 2025;138:332-342. doi: 10.1097/CM9.0000000000003004. (PMID: 10.1097/CM9.0000000000003004)
Cui C, Gan Y, Gu L, Wilson J, Liu Z, Zhang B, et al. P16-specific DNA methylation by engineered zinc finger methyltransferase inactivates gene transcription and promotes cancer metastasis. Genome Biol 2015;16:252. doi: 10.1186/s13059-015-0819-6. (PMID: 10.1186/s13059-015-0819-6)
Lee DD, Leão R, Komosa M, Gallo M, Zhang CH, Lipman T, et al. DNA hypermethylation within TERT promoter upregulates TERT expression in cancer. J Clin Invest 2019;129:1801. doi: 10.1172/JCI121303. (PMID: 10.1172/JCI121303)
Chen D, Wang J, Li Y, Xu C, Fanzheng M, Zhang P, et al. LncRNA NEAT1 suppresses cellular senescence in hepatocellular carcinoma via KIF11-dependent repression of CDKN2A. Clin Transl Med 2023;13:e1418. doi: 10.1002/ctm2.1418. (PMID: 10.1002/ctm2.1418)
Meguro S, Johmura Y, Wang TW, Kawakami S, Tanimoto S, Omori S, et al. Preexisting senescent fibroblasts in the aged bladder create a tumor-permissive niche through CXCL12 secretion. Nat Aging 2024;4:1582-1597. doi: 10.1038/s43587-024-00704-1. (PMID: 10.1038/s43587-024-00704-1)
Wang L, Lankhorst L, Bernards R. Exploiting senescence for the treatment of cancer. Nat Rev Cancer 2022;22:340-355. doi: 10.1038/s41568-022-00450-9. (PMID: 10.1038/s41568-022-00450-9)
Toso A, Revandkar A, Di Mitri D, Guccini I, Proietti M, Sarti M, et al. Enhancing chemotherapy efficacy in Pten-deficient prostate tumors by activating the senescence-associated antitumor immunity. Cell Rep 2014;9:75-89. doi: 10.1016/j.celrep.2014.08.044. (PMID: 10.1016/j.celrep.2014.08.044)
Lai P, Liu L, Bancaro N, Troiani M, Calì B, Li Y, et al. Mitochondrial DNA released by senescent tumor cells enhances PMN-MDSC-driven immunosuppression through the cGAS-STING pathway. Immunity 2025;58:811-825.e7. doi: 10.1016/j.immuni.2025.03.005. (PMID: 10.1016/j.immuni.2025.03.005)
Ruhland MK, Loza AJ, Capietto AH, Luo X, Knolhoff BL, Flanagan KC, et al. Stromal senescence establishes an immunosuppressive microenvironment that drives tumorigenesis. Nat Commun 2016;7:11762. doi: 10.1038/ncomms11762. (PMID: 10.1038/ncomms11762)
Chen Z, Zhou J, Wu Y, Chen F, Li J, Tao L, et al. METTL3 promotes cellular senescence of colorectal cancer via modulation of CDKN2B transcription and mRNA stability. Oncogene 2024;43:976-991. doi: 10.1038/s41388-024-02956-y. (PMID: 10.1038/s41388-024-02956-y)
Shen H, Chen Y, Xu M, Zhou J, Huang C, Wang Z, et al. Cellular senescence gene TACC3 associated with colorectal cancer risk via genetic and DNA methylated alteration. Arch Toxicol 2024;98:1499-1513. doi: 10.1007/s00204-024-03702-9. (PMID: 10.1007/s00204-024-03702-9)
Li J, Kluiver J, Osinga J, Westers H, van Werkhoven MB, Seelen MA, et al. Functional studies on primary tubular epithelial cells indicate a tumor suppressor role of SETD2 in clear cell renal cell carcinoma. Neoplasia 2016;18:339-346. doi: 10.1016/j.neo.2016.04.005. (PMID: 10.1016/j.neo.2016.04.005)
Abramenkovs A, Hariri M, Spiegelberg D, Nilsson S, Stenerlöw B. Ra-223 induces clustered DNA damage and inhibits cell survival in several prostate cancer cell lines. Transl Oncol 2022;26:101543. doi: 10.1016/j.tranon.2022.101543. (PMID: 10.1016/j.tranon.2022.101543)
Laranjeira ABA, Hollingshead MG, Nguyen D, Kinders RJ, Doroshow JH, Yang SX. DNA damage, demethylation and anticancer activity of DNA methyltransferase (DNMT) inhibitors. Sci Rep 2023;13:5964. doi: 10.1038/s41598-023-32509-4. (PMID: 10.1038/s41598-023-32509-4)
Berdasco M, Esteller M. Clinical epigenetics: seizing opportunities for translation. Nat Rev Genet 2019;20:109-127. doi: 10.1038/s41576-018-0074-2. (PMID: 10.1038/s41576-018-0074-2)
Bates SE. Epigenetic therapies for cancer. N Engl J Med 2020;383:650-663. doi: 10.1056/NEJMra1805035. (PMID: 10.1056/NEJMra1805035)
Wang P, Xiao R, Chen J, Guan P, Heng HL, Liu L, et al. PARP inhibitor augments anti-tumor efficacy of DNMT inhibitor by inducing senescence in cholangiocarcinoma. Int J Biol Sci 2025;21:3649-3665. doi: 10.7150/ijbs.110947. (PMID: 10.7150/ijbs.110947)
Sharma D, Bhartiya D. Aged mice ovaries harbor stem cells and germ cell nests but fail to form follicles. J Ovarian Res 2022;15:37. doi: 10.1186/s13048-022-00968-4. (PMID: 10.1186/s13048-022-00968-4)
Campisi M, Cannella L, Visioli F, Pavanello S. A systematic review of food-derived DNA methyltransferase modulators: Mechanistic insights and perspectives for healthy aging. Adv Nutr 2025;16:100521. doi: 10.1016/j.advnut.2025.100521. (PMID: 10.1016/j.advnut.2025.100521)
Falckenhayn C, Bienkowska A, Söhle J, Wegner K, Raddatz G, Kristof B, et al. Identification of dihydromyricetin as a natural DNA methylation inhibitor with rejuvenating activity in human skin. Front Aging 2024;4:1258184. doi: 10.3389/fragi.2023.1258184. (PMID: 10.3389/fragi.2023.1258184)
Pereira B, Correia FP, Alves IA, Costa M, Gameiro M, Martins AP, et al. Epigenetic reprogramming as a key to reverse ageing and increase longevity. Ageing Res Rev 2024;95:102204. doi: 10.1016/j.arr.2024.102204. (PMID: 10.1016/j.arr.2024.102204)
Wang C, Wang Y, Gu Y, Zhu Y, Yin R, Li Y, et al. SPI1 facilitates microfracture-mediated cartilage regeneration in the elderly by enhancing bone marrow stromal cells ctemness. J Tissue Eng 2025;16:20417314241311073. doi: 10.1177/20417314241311073. (PMID: 10.1177/20417314241311073)
Li Q, Zhai Y, Man X, Zhang S, An X. Inhibition of DNA methyltransferase by RG108 promotes pluripotency-related character of porcine bone marrow mesenchymal stem cells. Cell Reprogram 2020;22:82-89. doi: 10.1089/cell.2019.0060. (PMID: 10.1089/cell.2019.0060)
Roato I, Baima G, Orrico C, Mosca Balma A, Alotto D, Romano F, et al. Senescent markers expressed by periodontal ligament-derived stem cells (PDLSCs) harvested from patients with periodontitis can be rejuvenated by RG108. Biomedicines 2023;11:2535. doi: 10.3390/biomedicines11092535. (PMID: 10.3390/biomedicines11092535)
Govarthanan K, Gupta PK, Ramasamy D, Kumar P, Mahadevan S, Verma RS. DNA methylation microarray uncovers a permissive methylome for cardiomyocyte differentiation in human mesenchymal stem cells. Genomics 2020;112:1384-1395. doi: 10.1016/j.ygeno.2019.08.007. (PMID: 10.1016/j.ygeno.2019.08.007)
Duda M, Samiec M. Can Molecular attributes of mammalian granulosa cells and ovarian putative stem cells predestine them to be a promising tool for tissue engineering and regenerative medicine? Int J Mol Sci 2025;26:10667. doi: 10.3390/ijms262110667. (PMID: 10.3390/ijms262110667)
Farag A, Koung Ngeun S, Kaneda M, Aboubakr M, Tanaka R. Optimizing cardiomyocyte differentiation: Comparative analysis of bone marrow and adipose-derived mesenchymal stem cells in rats using 5-Azacytidine and low-dose FGF and IGF treatment. Biomedicines 2024;12:1923. doi: 10.3390/biomedicines12081923. (PMID: 10.3390/biomedicines12081923)
Morschhauser F, Tilly H, Chaidos A, McKay P, Phillips T, Assouline S, et al. Tazemetostat for patients with relapsed or refractory follicular lymphoma: An open-label, single-arm, multicentre, phase 2 trial. Lancet Oncol 2020;21:1433-1442. doi: 10.1016/S1470-2045(20)30441-1. (PMID: 10.1016/S1470-2045(20)30441-1)
Lavudi K, Nuguri SM, Olverson Z, Dhanabalan AK, Patnaik S, Kokkanti RR. Targeting the retinoic acid signaling pathway as a modern precision therapy against cancers. Front Cell Dev Biol 2023;11:1254612. doi: 10.3389/fcell.2023.1254612. (PMID: 10.3389/fcell.2023.1254612)
Mushtaq M, Liaño-Pons J, Wang J, Alzrigat M, Yuan Y, Ruiz-Pérez MV, et al. EZH2 inhibition sensitizes retinoic acid-driven senescence in synovial sarcoma. Cell Death Dis 2024;15:836. doi: 10.1038/s41419-024-07176-6. (PMID: 10.1038/s41419-024-07176-6)
Eich ML, Athar M, Ferguson JE, Varambally S. EZH2-targeted therapies in cancer: Hype or a reality. Cancer Res 2020;80:5449-5458. doi: 10.1158/0008-5472.CAN-20-2147. (PMID: 10.1158/0008-5472.CAN-20-2147)
Yasuda T, Koiwa M, Yonemura A, Miyake K, Kariya R, Kubota S, et al. Inflammation-driven senescence-associated secretory phenotype in cancer-associated fibroblasts enhances peritoneal dissemination. Cell Rep 2021;34:108779. doi: 10.1016/j.celrep.2021.108779. (PMID: 10.1016/j.celrep.2021.108779)
Chhabra Y, Fane ME, Pramod S, Hüser L, Zabransky DJ, Wang V, et al. Sex-dependent effects in the aged melanoma tumor microenvironment influence invasion and resistance to targeted therapy. Cell 2024;187:6016-6034.e25. doi: 10.1016/j.cell.2024.08.013. (PMID: 10.1016/j.cell.2024.08.013)
Horitani K, Iwasaki M, Kishimoto H, Wada K, Nakano M, Park H, et al. Repetitive spikes of glucose and lipid induce senescence-like phenotypes of bone marrow stem cells through H3K27me3 demethylase-mediated epigenetic regulation. Am J Physiol Heart Circ Physiol 2021;321:H920-932. doi: 10.1152/ajpheart.00261.2021. (PMID: 10.1152/ajpheart.00261.2021)
Li S, Li Q, Xiang H, Wang C, Zhu Q, Ruan D, et al. H2S donor SPRC ameliorates cardiac aging by suppression of JMJD3, a histone demethylase. Antioxid Redox Signal 2025;42:301-320. doi: 10.1089/ars.2024.0605. (PMID: 10.1089/ars.2024.0605)
Huang Y, Zhang H, Wang L, Tang C, Qin X, Wu X, et al. JMJD3 acts in tandem with KLF4 to facilitate reprogramming to pluripotency. Nat Commun 2020;11:5061. doi: 10.1038/s41467-020-18900-z. (PMID: 10.1038/s41467-020-18900-z)
Nakata Y, Ueda T, Sera Y, Koizumi M, Imamura K, Kanai A, et al. JMJD3-mediated senescence is required to overcome stress-induced hematopoietic defects. EMBO Rep 2025;26:3831-3855. doi: 10.1038/s44319-025-00502-9. (PMID: 10.1038/s44319-025-00502-9)
Guillermo ARR, Chocian K, Gavriilidis G, Vandamme J, Salcini AE, Mellor J, et al. H3K27 modifiers regulate lifespan in C. elegans in a context-dependent manner. BMC Biol 2021;19:59. doi: 10.1186/s12915-021-00984-8. (PMID: 10.1186/s12915-021-00984-8)
Li G, Ma L, He S, Luo R, Wang B, Zhang W, et al. WTAP-mediated m6A modification of lncRNA NORAD promotes intervertebral disc degeneration. Nat Commun 2022;13:1469. doi: 10.1038/s41467-022-28990-6. (PMID: 10.1038/s41467-022-28990-6)
Wu O, Jin Y, Zhang Z, Zhou H, Xu W, Chen L, et al. KMT2A regulates the autophagy-GATA4 axis through METTL3-mediated m6A modification of ATG4a to promote NPCs senescence and IVDD progression. Bone Res 2024;12:67. doi: 10.1038/s41413-024-00373-1. (PMID: 10.1038/s41413-024-00373-1)
Shi MQ, Xu Y, Fu X, Pan DS, Lu XP, Xiao Y, et al. Advances in targeting histone deacetylase for treatment of solid tumors. J Hematol Oncol 2024;17:37. doi: 10.1186/s13045-024-01551-8. (PMID: 10.1186/s13045-024-01551-8)
Whittaker SJ, Demierre MF, Kim EJ, Rook AH, Lerner A, Duvic M, et al. Final results from a multicenter, international, pivotal study of romidepsin in refractory cutaneous T-cell lymphoma. J Clin Oncol 2010;28:4485-4491. doi: 10.1200/JCO.2010.28.9066. (PMID: 10.1200/JCO.2010.28.9066)
O’Connor OA, Horwitz S, Masszi T, Van Hoof A, Brown P, Doorduijn J, et al. Belinostat in patients with relapsed or refractory peripheral T-Cell lymphoma: Results of the pivotal phase II BELIEF (CLN-19) study. J Clin Oncol 2015;33:2492-2499. doi: 10.1200/JCO.2014.59.2782. (PMID: 10.1200/JCO.2014.59.2782)
San-Miguel JF, Hungria VTM, Yoon SS, Beksac M, Dimopoulos MA, Elghandour A, et al. Overall survival of patients with relapsed multiple myeloma treated with panobinostat or placebo plus bortezomib and dexamethasone (the PANORAMA 1 trial): A randomised, placebo-controlled, phase 3 trial. Lancet Haematol 2016;3:e506-515. doi: 10.1016/S2352-3026(16)30147-8. (PMID: 10.1016/S2352-3026(16)30147-8)
Mabe NW, Perry JA, Malone CF, Stegmaier K. Pharmacological targeting of the cancer epigenome. Nat Cancer 2024;5:844-865. doi: 10.1038/s43018-024-00777-2. (PMID: 10.1038/s43018-024-00777-2)
McIntyre RL, Daniels EG, Molenaars M, Houtkooper RH, Janssens GE. From molecular promise to preclinical results: HDAC inhibitors in the race for healthy aging drugs. EMBO Mol Med 2019;11:e9854. doi: 10.15252/emmm.201809854. (PMID: 10.15252/emmm.201809854)
Krishnan V, Chow MZY, Wang Z, Zhang L, Liu B, Liu X, et al. Histone H4 lysine 16 hypoacetylation is associated with defective DNA repair and premature senescence in Zmpste24-deficient mice. Proc Natl Acad Sci U S A 2011;108:12325-12330. doi: 10.1073/pnas.1102789108. (PMID: 10.1073/pnas.1102789108)
Al-Mansour F, Alraddadi A, He B, Saleh A, Poblocka M, Alzahrani W, et al. Characterization of the HDAC/PI3K inhibitor CUDC-907 as a novel senolytic. Aging (Albany NY) 2023;15:2373-2394. doi: 10.18632/aging.204616. (PMID: 10.18632/aging.204616)
Wang T, Li X, Sun SL. EX527, a Sirt-1 inhibitor, induces apoptosis in glioma via activating the p53 signaling pathway. Anticancer Drugs 2020;31:19-26. doi: 10.1097/CAD.0000000000000824. (PMID: 10.1097/CAD.0000000000000824)
Abdulkhaliq AA, Alasiri G, Khan J, Ajoolabady A, Tuomilehto J, Henninger N, et al. SIRT1 in aging and diseases. J Cell Biochem 2025;126:e70069. doi: 10.1002/jcb.70069. (PMID: 10.1002/jcb.70069)
Dong W, Zhang K, Gong Z, Luo T, Li J, Wang X, et al. N-acetylcysteine delayed cadmium-induced chronic kidney injury by activating the sirtuin 1-P53 signaling pathway. Chem Biol Interact 2023;369:110299. doi: 10.1016/j.cbi.2022.110299. (PMID: 10.1016/j.cbi.2022.110299)
Moraes DS, Moreira DC, Andrade J, Santos S. Sirtuins, brain and cognition: A review of resveratrol effects. IBRO Rep 2020;9:46-51. doi: 10.1016/j.ibror.2020.06.004. (PMID: 10.1016/j.ibror.2020.06.004)
Leite JA, Ghirotto B, Targhetta VP, de Lima J, Câmara N. Sirtuins as pharmacological targets in neurodegenerative and neuropsychiatric disorders. Br J Pharmacol 2022;179:1496-1511. doi: 10.1111/bph.15570. (PMID: 10.1111/bph.15570)
Tai S, Zhou Y, Fu L, Ding H, Zhou Y, Yin Z, et al. Dapagliflozin impedes endothelial cell senescence by activating the SIRT1 signaling pathway in type 2 diabetes. Heliyon 2023;9:e19152. doi: 10.1016/j.heliyon.2023.e19152. (PMID: 10.1016/j.heliyon.2023.e19152)
Wang H, Sun Y, Pi C, Yu X, Gao X, Zhang C, et al. Nicotinamide mononucleotide supplementation improves mitochondrial dysfunction and rescues cellular senescence by NAD+/Sirt3 pathway in mesenchymal stem cells. Int J Mol Sci 2022;23:14739. doi: 10.3390/ijms232314739. (PMID: 10.3390/ijms232314739)
Takahashi K, Yamanaka S. Induction of pluripotent stem cells from mouse embryonic and adult fibroblast cultures by defined factors. Cell 2006;126:663-676. doi: 10.1016/j.cell.2006.07.024. (PMID: 10.1016/j.cell.2006.07.024)
Lu YR, Tian X, Sinclair DA. The information theory of aging. Nat Aging 2023;3:1486-1499. doi: 10.1038/s43587-023-00527-6. (PMID: 10.1038/s43587-023-00527-6)
Ocampo A, Reddy P, Martinez-Redondo P, Platero-Luengo A, Hatanaka F, Hishida T, et al. In vivo amelioration of age-associated hallmarks by partial reprogramming. Cell 2016;167:1719-1733. doi: 10.1016/j.cell.2016.11.052. (PMID: 10.1016/j.cell.2016.11.052)
Lu Y, Brommer B, Tian X, Krishnan A, Meer M, Wang C, et al. Reprogramming to recover youthful epigenetic information and restore vision. Nature 2020;588:124-129. doi: 10.1038/s41586-020-2975-4. (PMID: 10.1038/s41586-020-2975-4)
Yang JH, Petty CA, Dixon-McDougall T, Lopez MV, Tyshkovskiy A, Maybury-Lewis S, et al. Chemically induced reprogramming to reverse cellular aging. Aging (Albany NY) 2023;15:5966-5989. doi: 10.18632/aging.204896. (PMID: 10.18632/aging.204896)
Ladewig J, Mertens J, Kesavan J, Doerr J, Poppe D, Glaue F, et al. Small molecules enable highly efficient neuronal conversion of human fibroblasts. Nat Methods 2012;9:575–578. doi: 10.1038/nmeth.1972. (PMID: 10.1038/nmeth.1972)
Contributed Indexing: Keywords: Age-related diseases; Cellular senescence; Epigenomics; Senolytics; Senomorphics
Substance Nomenclature: 0 (Senotherapeutics)
Entry Date(s): Date Created: 20260318 Date Completed: 20260705 Latest Revision: 20260726
Update Code: 20260726
PubMed Central ID: PMC13331420
DOI: 10.1097/CM9.0000000000004042
PMID: 41850873
Βάση Δεδομένων: MEDLINE
Περιγραφή
ISSN:2542-5641
DOI:10.1097/CM9.0000000000004042