Editorial & Opinion

Diagnostic interpretation of CFH expression in pan-cancer analyses: the importance of factor H-like 1 isoform resolution.

Λεπτομέρειες βιβλιογραφικής εγγραφής
Τίτλος: Diagnostic interpretation of CFH expression in pan-cancer analyses: the importance of factor H-like 1 isoform resolution.
Συγγραφείς: Clark SJ; Department of Ophthalmology, Institute for Ophthalmic Research, Eberhard Karls University of Tübingen, Tübingen, Germany. simon.clark@uni-tuebingen.de.; University Eye Clinic, Eberhard Karls University of Tübingen, Tübingen, Germany. simon.clark@uni-tuebingen.de.; Lydia Becker Institute of Immunology and Inflammation, University of Manchester, Manchester, UK. simon.clark@uni-tuebingen.de.
Πηγή: BMC cancer [BMC Cancer] 2026 Oct 11; Vol. 26 (1). Date of Electronic Publication: 2026 Oct 11.
Τύπος έκδοσης: Letter
Γλώσσα: English
Στοιχεία περιοδικού: Publisher: BioMed Central Country of Publication: England NLM ID: 100967800 Publication Model: Electronic Cited Medium: Internet ISSN: 1471-2407 (Electronic) Linking ISSN: 14712407 NLM ISO Abbreviation: BMC Cancer Subsets: MEDLINE
Imprint Name(s): Original Publication: London : BioMed Central, [2001-
Ιατρικοί όροι (MeSH): Complement Factor H*/genetics , Complement Factor H*/metabolism , Neoplasms*/diagnosis , Neoplasms*/genetics , Neoplasms*/metabolism , Biomarkers, Tumor*/genetics , Biomarkers, Tumor*/metabolism, Protein Isoforms/genetics ; Protein Isoforms/metabolism ; Humans ; Gene Expression Regulation, Neoplastic
Περίληψη: Recent pan-cancer analyses have identified Complement Factor H (CFH) expression as an immune-related and prognostic biomarker. However, interpretation of CFH transcriptional data requires consideration of isoform specificity. The CFH gene encodes both full-length factor H (FH) and the biologically active splice isoform factor H-like 1 (FHL-1), which differ in structure and tissue localization. Common transcriptional and knockdown approaches do not distinguish between these isoforms, potentially introducing biological heterogeneity into diagnostic and prognostic assessments. Isoform-resolved analyses may therefore enhance the specificity and clinical utility of CFH-based biomarkers in oncology.
(© 2026. The Author(s).)
Competing Interests: Declarations. Ethics approval and consent to participate: Not applicable. Consent for publication: Not applicable. Competing interests: The authors declare no competing interests.
References: Clin Cancer Res. 2021 Dec 1;27(23):6514-6528. (PMID: 34479957)
Immunol Rev. 2023 Jan;313(1):25-45. (PMID: 36382387)
Cancer Res. 2004 Sep 1;64(17):6310-8. (PMID: 15342420)
Front Immunol. 2024 Feb 12;15:1135490. (PMID: 38410512)
J Immunol. 2014 Nov 15;193(10):4962-70. (PMID: 25305316)
BMC Cancer. 2025 Dec 26;26(1):142. (PMID: 41454282)
Int J Oncol. 2011 Jul;39(1):161-8. (PMID: 21503575)
Semin Immunopathol. 2018 Jan;40(1):65-74. (PMID: 28948331)
Substance Nomenclature: 80295-65-4 (Complement Factor H)
0 (Protein Isoforms)
0 (Biomarkers, Tumor)
0 (CFH protein, human)
Entry Date(s): Date Created: 20261010 Date Completed: 20261010 Latest Revision: 20261015
Update Code: 20261015
PubMed Central ID: PMC13654215
DOI: 10.1186/s12885-026-17134-4
PMID: 42859169
Βάση Δεδομένων: MEDLINE
Περιγραφή
ISSN:1471-2407
DOI:10.1186/s12885-026-17134-4