Role of Fanconi anemia/BRCA pathway genes in hepatocellular carcinoma chemoresistance

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Aim: To investigate the expression of DNA repair genes and the impact of the breast cancer 1, early onset (BRCA1) protein on chemoresistance of hepatocellular carcinoma (HCC). Methods: Microarray gene expression datasets were analyzed using the gene set enrichment analysis method. BRCA1 protein was tested by Western blotting. Response of HCC cells to interstrand cross-links was investigated by cell viability assay following exposure to mitomycin C, cisplatin, and melphalan. Effects of BRCA1 ectopic expression were studied in HepG2 cells with BRCA1-expression plasmids. Effects of BRCA1 downregulation were studied in SNU449 cells with BRCA1-specific siRNAs. Response of transfected SNU449 cells to mitomycin C was analyzed by cell viability tests and cell cycle analysis using flow cytometry. Results: Expression of Fanconi anemia and double-stranded DNA break repair genes was significantly upregulated in HCC tumors. This upregulation displayed a gradual amplification during tumor progression. BRCA1 and BRCA2 genes were among consistently upregulated genes. Epithelial-like HCC cells had low BRCA1 expression and low chemoresistance, whereas mesenchymal-like HCC cells had high BRCA1 expression and increased chemoresistance. Ectopic expression of BRCA1 increased the chemoresistance of epithelial-like HepG2 cells. Conversely, BRCA1 knockdown chemosensitized mesenchymal-like SNU449 cells. Chemosensitization of SNU449 cells was due to cell cycle arrest at 4N stage. Conclusion: Increased expression of Fanconi anemia and double-stranded DNA repair genes such as BRCA1 is a novel mechanism of HCC chemoresistance. However, functional inactivation of BRCA1 expression is sufficient to reverse such chemoresistance. © 2016 The Japan Society of Hepatology

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RDL Kalıcı Bağlantı (PID)
https://rdlopen.rawdatalibrary.net/r/ebyu/14990Resmi atıflarda kullanılan kalıcı adres
DOI
https://doi.org/10.1111/hepr.12675Yayıncı resmi DOI adresi
Tam Kayıt
AlanDeğerDil
dc.contributor.authorFerroudj, Sana
dc.contributor.authorYildiz, Gokhan
dc.contributor.authorBouras, Mourad
dc.contributor.authorIscan, Evin
dc.contributor.authorEkin, Umut
dc.contributor.authorOzturk, Mehmet
dc.date.accessioned2026-10-18T20:29:47.258073371Z
dc.date.available2026-10-18T20:29:47.258073371Z
dc.date.issued2016
dc.description.abstractAim: To investigate the expression of DNA repair genes and the impact of the breast cancer 1, early onset (BRCA1) protein on chemoresistance of hepatocellular carcinoma (HCC). Methods: Microarray gene expression datasets were analyzed using the gene set enrichment analysis method. BRCA1 protein was tested by Western blotting. Response of HCC cells to interstrand cross-links was investigated by cell viability assay following exposure to mitomycin C, cisplatin, and melphalan. Effects of BRCA1 ectopic expression were studied in HepG2 cells with BRCA1-expression plasmids. Effects of BRCA1 downregulation were studied in SNU449 cells with BRCA1-specific siRNAs. Response of transfected SNU449 cells to mitomycin C was analyzed by cell viability tests and cell cycle analysis using flow cytometry. Results: Expression of Fanconi anemia and double-stranded DNA break repair genes was significantly upregulated in HCC tumors. This upregulation displayed a gradual amplification during tumor progression. BRCA1 and BRCA2 genes were among consistently upregulated genes. Epithelial-like HCC cells had low BRCA1 expression and low chemoresistance, whereas mesenchymal-like HCC cells had high BRCA1 expression and increased chemoresistance. Ectopic expression of BRCA1 increased the chemoresistance of epithelial-like HepG2 cells. Conversely, BRCA1 knockdown chemosensitized mesenchymal-like SNU449 cells. Chemosensitization of SNU449 cells was due to cell cycle arrest at 4N stage. Conclusion: Increased expression of Fanconi anemia and double-stranded DNA repair genes such as BRCA1 is a novel mechanism of HCC chemoresistance. However, functional inactivation of BRCA1 expression is sufficient to reverse such chemoresistance. © 2016 The Japan Society of Hepatology
dc.description.sponsorshipTHIS WORK WAS supported by La Ligue Nationale Contre le Cancer (Equipe labelisee) and Scientific and Technological Research Council of Turkey (TUBITAK) Project No: 113S389 with additional support from the Turkish Academy of Sciences. Sana Ferroudj was supported by a Fellowship of the Ministry of Higher Education and Scientific Research (Algeria). GokhanYildiz was supported by TUBITAK (BIDEB-2214) and European Molecular Biology Organization short-term fellowships. We thank Dr. Isik Yulug for providing pCMVmycBRCA1 plasmid.
dc.identifier.doi10.1111/hepr.12675
dc.identifier.eissn1872-034X
dc.identifier.endpage1274
dc.identifier.issn1386-6346
dc.identifier.issue12
dc.identifier.pmid26885668
dc.identifier.scopus2-s2.0-84963533287
dc.identifier.startpage1264
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/ebyu/14990
dc.identifier.volume46
dc.identifier.wosWOS:000389451800010
dc.language.isoen
dc.publisherBlackwell Publishing Ltd
dc.relation.ispartofHepatology Research
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectBRCA1
dc.subjectchemosensitization
dc.subjectDSB DNA repair
dc.subjectFanconi anemia
dc.subjecthepatocellular cancer
dc.subjectinterstrand cross-linker drugs
dc.subjectBRCA1 protein
dc.subjectcisplatin
dc.subjectmelphalan
dc.subjectmitomycin
dc.subjectsmall interfering RNA
dc.subjectArticle
dc.subjectcell cycle
dc.subjectcell viability
dc.subjectcontrolled study
dc.subjectDNA repair
dc.subjectdouble stranded DNA break
dc.subjectdown regulation
dc.subjectdrug resistance
dc.subjectflow cytometry
dc.subjectG2 phase cell cycle checkpoint
dc.subjectgene expression regulation
dc.subjectHepG2 cell line
dc.subjecthuman
dc.subjecthuman cell
dc.subjectliver cell carcinoma
dc.subjectmicroarray analysis
dc.subjectpriority journal
dc.subjectprotein cross linking
dc.subjectprotein expression
dc.titleRole of Fanconi anemia/BRCA pathway genes in hepatocellular carcinoma chemoresistance
dc.typeArticle
dspace.entity.typePublication
rdl.citation.scopus18
rdl.citation.wos16
rdl.departmentDepartment of Medical Biology, Faculty of Medicine, Erzincan University, Erzincan, Turkey.
rdl.source.indexSCOPUS
rdl.source.indexWOS
rdl.source.indexPUBMED
rdl.wos.indexScience Citation Index Expanded (SCI-EXPANDED)