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    Academic Journal

    Πηγή: Obstetrics, Gynecology and Reproduction; Vol 17, No 4 (2023); 420-432 ; Акушерство, Гинекология и Репродукция; Vol 17, No 4 (2023); 420-432 ; 2500-3194 ; 2313-7347

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Circulating cell-free DNA in plasma of never smokers with advanced lung adenocarcinoma receiving gefitinib or standard chemotherapy as first-line therapy circulating DNA in prognosis of advanced NSCLC. Clin Cancer Res. 2011;17(15):5179–87. https://doi.org/10.1158/1078-0432.CCR-11-0400.; Demers M., Krause D.S., Schatzberg D. et al. Cancers predispose neutrophils to release extracellular DNA traps that contribute to cancerassociated thrombosis. Proc Natl Acad Sci U S A. 2012;109(32):13076– 81. https://doi.org/10.1073/pnas.1200419109.; Cools-Lartigue J., Spicer J., Najmeh S., Ferri L. Neutrophil extracellular traps in cancer progression. Cell Mol Life Sci. 2014;71(21):4179–94. https://doi.org/10.1007/s00018-014-1683-3.; Holdenrieder S., Stieber P., von Pawel J. et al. Circulating nucleosomes predict the response to chemotherapy in patients with advanced non–small cell lung cancer. 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Neutrophil extracellular traps in immunity and disease. Nat Rev Immunol. 2018;18(2):134. https://doi.org/10.1038/nri.2017.105.; Huang H., Zhang H., Onuma A.E., Tsung A. Neutrophil elastase and neutrophil extracellular traps in the tumor microenvironment. Adv Exp Med Biol. 2020;1263:13–23. https://doi.org/10.1007/978-3-030-44518-8_2.; Garley M., Jabłońska E., Dąbrowska D. NETs in cancer. Tumor Biol. 2016;37(11):14355–61. https://doi.org/10.1007/s13277-016-5328-z.; Bianchi M., Niemiec M.J., Siler U. et al. Restoration of anti-Aspergillus defense by neutrophil extracellular traps in human chronic granulomatous disease after gene therapy is calprotectin-dependent. J Allergy Clin Immunol. 2011;127(5):1243–52.e7. https://doi.org/10.1016/j.jaci.2011.01.021.; Wang S., Li Y., Xing C. et al. Tumor microenvironment in chemoresistance, metastasis and immunotherapy of pancreatic cancer. Am J Cancer Res. 2020;10(7):1937–53.; Hedrick C.C., Malanchi I. Neutrophils in cancer: heterogeneous and multifaceted. Nat Rev Immunol. 2022;22(3):173–87. https://doi.org/10.1038/s41577-021-00571-6.; Kan M., Imaoka H., Watanabe K. et al. Chemotherapy-induced neutropenia as a prognostic factor in patients with pancreatic cancer treated with gemcitabine plus nab-paclitaxel: a retrospective cohort study. Cancer Chemother Pharmacol. 2020;86(2):203–10. https://doi.org/10.1007/s00280-020-04110-3.; Kasi P.M., Grothey A. Chemotherapy-induced neutropenia as a prognostic and predictive marker of outcomes in solid-tumor patients. Drugs. 2018;78(7):737–45. https://doi.org/10.1007/s40265-018-0909-3; Zhang Y., Guoqiang L., Sun M., Lu X. Targeting and exploitation of tumorassociated neutrophils to enhance immunotherapy and drug delivery for cancer treatment. Cancer Biol Med. 2020;17(1):32–43. https://doi.org/10.20892/j.issn.2095-3941.2019.0372.; Vossenaar E.R., Zendman A.J., van Venrooij W.J., Pruijn G.J. PAD, a growing family of citrullinating enzymes: genes, features and involvement in disease. Bioessays. 2003;25(11):1106–18. https://doi.org/10.1002/bies.10357.; Hensen S.M., Pruijn G.J. Methods for the detection of peptidylarginine deiminase (PAD) activity and protein citrullination. Mol Cel Proteomics. 2014;13(2):388–96. https://doi.org/10.1074/mcp.R113.033746.; van Beers J.J., Zendman A.J., Raijmakers R. et al. Peptidylarginine deiminase expression and activity in PAD2 knock-out and PAD4-low mice. Biochimie. 2013;95(2):299–308. https://doi.org/10.1016/j.biochi.2012.09.029.; Lewis H.D., Liddle J., Coote J.E. et al. Inhibition of PAD4 activity is sufficient to disrupt mouse and human NET formation. Nat Chem Biol. 2015;11(3):189–91. https://doi.org/10.1038/nchembio.1735.; Martinod K., Demers M., Fuchs T.A. et al. Neutrophil histone modification by peptidylarginine deiminase 4 is critical for deep vein thrombosis in mice. Proc Natl Acad Sci U S A. 2013;110(21):8674–9. https://doi.org/10.1073/pnas.1301059110.; Lysov Z., Dwivedi D.J., Gould T.J., Liaw P.C. Procoagulant effects of lung cancer chemotherapy: impact on microparticles and cell-free DNA. Blood Coagul Fibrinolysis. 2017;28(1):72–82. https://doi.org/10.1097/MBC.0000000000000546.; Lysov Z., Swystun L.L., Kuruvilla S. et al. Lung cancer chemotherapy agents increase procoagulant activity via protein disulfide isomerasedependent tissue factor decryption. Blood Coagul Fibrinolysis. 2015;26(1):36–45. https://doi.org/10.1097/MBC.0000000000000145.; Wang H.-J., Huang H., Chuang Y.-C., Huang H.-C. Paclitaxel induces up-regulation of tissue factor in human aortic endothelial cells. Int Immunopharmacol. 2009;9(1):144–7. https://doi.org/10.1016/j.intimp.2008.10.003.; Hakkim A., Fürnrohr B.G., Amann K. et al. Impairment of neutrophil extracellular trap degradation is associated with lupus nephritis. Proc Natl Acad Sci U S A. 2010;107(21):9813–18. https://doi.org/10.1073/pnas.0909927107.; Farrera C., Fadeel B. Macrophage clearance of neutrophil extracellular traps is a silent process. J Immunol. 2013;191(5):2647–56. https://doi.org/10.4049/jimmunol.1300436; Stoetzer O.J., Fersching D.M., Salat C. et al. Prediction of response to neoadjuvant chemotherapy in breast cancer patients by circulating apoptotic biomarkers nucleosomes, DNAse, cytokeratin-18 fragments and survivin. Cancer Lett. 2013;336(1):140–8. https://doi.org/10.1016/j.canlet.2013.04.013.; Longstaff C., Varjú I., Sótonyi P. et al. Mechanical stability and fibrinolytic resistance of clots containing fibrin, DNA, and histones. J Biol Chem. 2013;288(10):6946–56. https://doi.org/10.1074/jbc.M112.404301.; Varjú I., Longstaff C., Szabó L. et al. DNA, histones and neutrophil extracellular traps exert anti-fibrinolytic effects in a plasma environment. Thromb Haemost. 2015;113(6):1289–98. https://doi.org/10.1160/TH14-08-0669.; Fuchs T.A., Brill A., Duerschmied D. et al. Extracellular DNA traps promote thrombosis. Proc Natl Acad Sci U S A. 2010;107(36):15880–5. https://doi.org/10.1073/pnas.1005743107.; Schiff P.B., Fant J., Horwitz S.B. Promotion of microtubule assembly in vitro by taxol. Nature. 1979;277(5698):665–7. https://doi.org/10.1038/277665a0.; Nogales E., Grayer Wolf S., Khan I.A. et al. Structure of tubulin at 6.5 Å and location of the taxol-binding site. Nature. 1995;375(6530):424–7. https://doi.org/10.1038/375424a0.; Nogales E. Structural insights into microtubule function. Annu Rev Biochem. 2000;69:277–302. https://doi.org/10.1146/annurev.biochem.69.1.277.; Schiff P.B., Horwitz S.B. Taxol stabilizes microtubules in mouse fibroblast cells. Proc Natl Acad Sci U S A. 1980;77(3):1561–5. https://doi.org/10.1073/pnas.77.3.1561.; Marupudi N.I., Han J.E., Li K.W. et al. Paclitaxel: a review of adverse toxicities and novel delivery strategies. Expert Opin Drug Saf. 2007;6(5):609–21. https://doi.org/10.1517/14740338.6.5.609.; Knox R.J., Friedlos F., Lydall D.A., Roberts J.J. Mechanism of cytotoxicity of anticancer platinum drugs: evidence that cis-diamminedichloroplatinum (II) and cis-diammine-(1,1-cyclobutanedicarboxylato) platinum (II) differ only in the kinetics of their interaction with DNA. Cancer Res.1986;46(4 Pt):1972–9.; Zhang Y., Chandra V., Riquelme Sanchez E. et al. Interleukin-17-induced neutrophil extracellular traps mediate resistance to checkpoint blockade in pancreatic cancer. J Exp Med. 2020;217(12):e20190354. https://doi.org/10.1084/jem.20190354.; Teijeira Á., Garasa S., Gato M. et al. CXCR1 and CXCR2 chemokine receptor agonists produced by tumors induce neutrophil extracellular traps that interfere with immune cytotoxicity. Immunity. 2020;52(5):856– 71.e8. https://doi.org/10.1016/j.immuni.2020.03.001.; Zhu T., Zou X., Yang C. et al. 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    Academic Journal

    Πηγή: Modern Rheumatology Journal; Том 10, № 3 (2016); 52-61 ; Современная ревматология; Том 10, № 3 (2016); 52-61 ; 2310-158X ; 1996-7012 ; 10.14412/1996-7012-2016-3

    Περιγραφή αρχείου: application/pdf

    Relation: https://mrj.ima-press.net/mrj/article/view/702/683; Smolen JS, Aletaha D, Bijlsma JW, et al. Treating rheumatoid arthritis to target: recommendations of an international task force. Ann Rheum Dis. 2010 Apr;69(4):631-7. doi:10.1136/ard.2009.123919. Epub 2010 Mar 9.; Каратеев ДЕ, Лучихина ЕЛ. Современная стратегия терапии ревматоидного артрита. Русский медицинский журнал. 2012;20(30):1504-9. [Karateev DE, Luchikhina EL. Modern strategy of therapy of rheumatoid arthritis. Russkii meditsinskii zhurnal. 2012;20(30):1504- 9. (In Russ.)].; Ермакова ЮА, Каратеев ДЕ, Лучихина ЕЛ, Демидова НВ. Динамика активности болезни, функционального статуса и рентгенологических изменений при раннем ревматоидном артрите: результаты 5-летнего наблюдения в рамках российской программы РАДИКАЛ. Научно-практическая ревматология. 2015;53(1):17-23. [Ermakova YuA, Karateev DE, Luchikhina EL, Demidova NV. Trends in disease activity, functional status, and radiographic changes in early rheumatoid arthritis: results of a 5-year follow-up within the russian RADIKAL program. Nauchno-prakticheskaya revmatologiya = Rheumatology Science and Practice. 2015;53(1):17-23. (In Russ.)]. doi:10.14412/1995-4484-2015- 17-23.; Каратеев ДЕ, Лучихина ЕЛ, Демидова НВ и др. Первое российское стратегическое исследование фармакотерапии ревматоидного артрита (РЕМАРКА): результаты лечения 130 больных в течение 12 месяцев. Научно-практическая ревматология. 2014;52(6):607-14. [Karateev DE, Luchikhina EL, Demidova NV, et al. The first russian strategic study of pharmacotherapy for rheumatoid arthritis (REMARCA TRIAL): results of 12-month treatment in 130 patients. Nauchno-prakticheskaya revmatologiya = Rheumatology Science and Practice. 2014;52(6):607-14. (In Russ.)]. doi:10.14412/1995- 4484-2014-607-614.; Каратеев ДЕ. Острые вопросы стратегии лечения ревматоидного артрита. Современная ревматология. 2015;9(1):84-92. [Karateev DE. Treatment strategy for rheumatoid arthritis: hot topics. Sovremennaya revmatologiya = Modern Rheumatology Journal. 2015;9(1):84-92. (In Russ.)]. doi:10.14412/1996-7012-2015-1-84-92.; Лучихина ЕЛ. Прогнозирование и длительное поддержание низкой активности заболевания на фоне терапии генно-инженерными биологическими препаратами при ревматоидном артрите. Современная ревматология. 2014;8(2):66-70. [Luchikhina EL. The prediction and longterm maintenance of low disease activity during therapy with disease modifying antiinflammatory drugs for rheumatoid arthritis. Sovremennaya revmatologiya = Modern Rheumatology Journal. 2014;8(2):66-70. (In Russ.)]. doi:10.14412/1996-7012-2014- 2-66-70; Каратеев ДЕ. Насколько Реально длительное сохранение лечебного эффекта ингибиторов ФНО-альфа? Фокус на иммуногенность. Современная ревматология. 2014;8(2):35-40. [Karateev DE. How real is the long-lasting effect of tumor necrosis factor α inhibitors? Focus on immunogenicity. Sovremennaya revmatologiya = Modern Rheumatology Journal. 2014;8(2):35-40. (In Russ.)]. doi:10.14412/1996-7012-2014-2-35-40.; Каратеев ДЕ. Новое направление в патогенетической терапии ревматоидного артрита: первый ингибитор Янус-киназ тофацитиниб. Современная ревматология. 2014;8(1):39-44. [Karateev DE. A new trend in pathogenetic treatment of rheumatoid arthritis: tofacitinib, the first inhibitor of Janus kinase. Sovremennaya revmatologiya = Modern Rheumatology Journal. 2014;8(1): 39-44. (In Russ.)]. doi:10.14412/1996-7012- 2014-1-39-44.; Насонов ЕЛ. Новые подходы к фармакотерапии ревматоидного артрита: тофацитиниб. Научно-практическая ревматология. 2014;52(2):209-21. [Nasonov EL. New approaches to pharmacotherapy of rheumatoid arthritis: Tofacitinib. Nauchnoprakticheskaya revmatologiya = Rheumatology Science and Practice. 2014;52(2):209-21. (In Russ.)]. doi:10.14412/1995-4484-2014- 209-221.; Fleischmann R, Kremer J, Cush J, et al. Placebo-controlled trial of tofacitinib monotherapy in rheumatoid arthritis. N Engl J Med. 2012 Aug 9;367(6):495-507.; Burmester GR, Blanco R, Charles-Schoerman C, et al. Tofacitinib (CP-690,550) in combination with methotrexate in patients with active rheumatoid arthritis with an inadequate response to tumour necrosis factor inhibitors: a randomised phase 3 trial. Lancet. 2013 Feb 9;381(9865):451-60. doi:10.1016/ S0140-6736(12)61424-X. Epub 2013 Jan 5.; Feist E, Burmester G. Small molecules targeting JAKs-a new approach in the treatment of rheumatoid arthritis. Rheumatology (Oxford). 2013 Aug;52(8):1352-7. doi:10.1093/ rheumatology/kes417. Epub 2013 Feb 1.; Дирескенели Х. Международный опыт применения тофацитиниба в реальной клинической практике. Современная ревматология. 2015;9(1M):5. [Direskeneli Kh. International experience of the use of tofacitinib in clinical practice. Sovremennaya revmatologiya = Modern Rheumatology journal. 2015;9(1M):5.]. doi:10.14412/1996- 7012- 2015-1-5.; Бабаева АР, Калинина ЕВ, Каратеев ДЕ. Опыт применения тофацитиниба в лечении резистентного ревматоидного артрита. Современная ревматология. 2015;9(2):28-32. [Babaeva AR, Kalinina EV, Karateev DE. Experience with tofacitinib in the treatment of resistant rheumatoid arthritis. Sovremennaya revmatologiya = Modern Rheumatology Journal. 2015;9(2):28-32. (In Russ.)]. doi:10.14412/1996-7012-2015-2-28-32.; Мясоутова Л. Клинический случай применения тофацитиниба. Современная ревматология. 2015;9(1M):8. [Myasoutova L. Clinical case of the use of tofacitinib. Sovremennaya revmatologiya = Modern Rheumatology Journal. 2015;9(1M):8.] doi:10.14412/1996-7012- 2015-1-8.; Демидова НВ, Лучихина ЕЛ, Каратеев ДЕ. Выраженный и быстрый терапевтический эффект тофацитиниба в комбинации с подкожным метотрексатом у пациентки с ревматоидным артритом, имеющей факторы неблагоприятного прогноза, резистентной к стандартным базисным средствам и генно-инженерным биологическим препаратам (клинический случай). Современная ревматология. 2016;10(1):37-40. [Demidova NV, Luchikhina EL, Karateev DE. The marked and rapid therapeutic effect of tofacitinib in combination with subcutaneous methotrexate in a rheumatoid arthritis patient with poor prognostic factors who is resistant to standard disease-modifying antirheumatic drugs and biologicals: A clinical case. Sovremennaya revmatologiya = Modern Rheumatology journal. 2016;10(1):37-40. (In Russ.)]. doi:10.14412/1996-7012-2016-1-37-40.; Лучихина ЕЛ, Каратеев ДЕ, Демидова НВ и др. Эффективность и безопасность терапии тофацитинибом у больных активным ревматоидным артритом с резистентностью к стандартной терапии: предварительные результаты открытого клинического исследования. Современная ревматология. 2016;10(2): 17-23. [Luchikhina EL, Karateev DE, Demidova NV, et al. Efficacy and safety of Tofacitinib in patients with active rheumatoid arthritis resistant to conventional therapy: Preliminary results of an open-label clinical trial. Sovremennaya revmatologiya = Modern Rheumatology journal. 2016;10(2):17-23.(In Russ.)]. doi:10.14412/1996-7012-2016- 2-17-23.; Насонов ЕЛ, Мазуров ВИ, Каратеев ДЕ и др. Проект рекомендаций по лечению ревматоидного артрита Общероссийской общественной организации «Ассоциация ревматологов России» – 2014 (часть 1). Научно-практическая ревматология. 2014;52(5):472-94. [Nasonov EL, Mazurov VI, Karateev DE, et al. Project: Recommendations on treatment of rheumatoid arthritis developed by All-Russian Public Organization «Association of rheumatologists of Russia» – 2014 (Part 1). Nauchno-prakticheskaya revmatologiya = Rheumatology Science and Practice. 2014;52(5):477-94. (In Russ.)]. doi:10.14412/1995-4484-2014-477-494.; Arnett FC, Edworthy SM, Bloch DA, et al. American Rheumatism Association 1987 revised criteria for the classification of rheumatoid arthritis. Arthritis Rheum. 1988 Mar;31(3):315-24.; Насонов ЕЛ, редактор. Ревматология. Клинические рекомендации. Москва: ГЭОТАР-Медиа; 2010. 752 c. [Nasonov EL, editor. Revmatologiya. Klinicheskie rekomendatsii [Rheumatology. Clinical guidelines]. Moscow: GEOTAR-Media; 2010. 752 p.]. 21. Aletaha D, Smolen J. The Simplified Disease Activity Index (SDAI) and the Clinical Disease Activity Index (CDAI): a review of their usefulness and validity in rheumatoid arthritis. Clin Exp Rheumatol. 2005;23(5 Suppl 39):S100-8.; Felson DT, Smolen JS, Wells G, et al. American College of Rheumatology/ European League against Rheumatism provisional definition of remission in rheumatoid arthritis for clinical trials. Ann Rheum Dis. 2011;70(3):404-13. doi:10.1136/ard.2011.149765.; Strand V, Fleischmann R, Alten RE, et al. ORAL START: effects of the oral JAK inhibitor tofacitinib monotherapy versus methotrexate on patient-reported outcomes in the phase 3 oral start trial of active rheumatoid arthritis. Ann Rheum Dis. 2013;72(Suppl 3):252, EULAR Congress abstr. THU0258.

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