Contribution of MRE11, RAD50, and NBS1 Genotypes to Bladder Cancer Susceptibility
- PMID: 40571318
- PMCID: PMC12216569
- DOI: 10.21873/cgp.20523
Contribution of MRE11, RAD50, and NBS1 Genotypes to Bladder Cancer Susceptibility
Abstract
Background/aim: Genome instability is a hallmark of cancer, often accelerated by defects in DNA damage responses. MRE11-RAD50-NBS1 (MRN) complex plays a crucial role in sensing and repairing DNA damage; however, there is limited literature on the involvement of MRN genotypes in bladder cancer (BLCA) susceptibility. This study aimed to elucidate the impact of MRN genotypes on the risk of BLCA.
Materials and methods: We genotyped 14 single nucleotide polymorphisms (SNPs) in MRN genes, including rs684507, rs2155209, rs10831234, rs13447720, rs601341 in MRE11, rs17166050, rs17772583, rs6871536, rs3798134, rs2244012 in RAD50, and rs1805794, rs2735383, rs1063053, rs1063054 in NBS1, among 375 BLCA cases and 375 controls, and evaluated their contributions to BLCA susceptibility.
Results: Among these SNPs, only NBS1 rs2735383 was significantly associated with BLCA risk (p for trend=0.0053), with both CG and CC genotypes conferring higher risks (OR=1.48 and 1.95, respectively). Subgroup analysis showed that NBS1 rs2735383 was associated with BLCA risk in individuals older than 55 years (OR=2.29, p=0.0053), smokers (OR=2.56, p=0.0026), alcohol drinkers (OR=3.25, p=0.0005), and those with muscle-invasive disease (OR=1.97, p=0.0243), but not in younger individuals, non-smokers, non-drinkers, or non-muscle-invasive cases.
Conclusion: NBS1 rs2735383 genotype may serve as a genetic biomarker for BLCA susceptibility, particularly in high-risk subpopulations, including elders, smokers, drinkers, and those with muscle-invasive disease.
Keywords: Bladder Cancer; Taiwan; double strand breaks; genotype; polymorphism.
Copyright © 2025, International Institute of Anticancer Research (Dr. George J. Delinasios), All rights reserved.
Conflict of interest statement
The Authors declare no conflicts of interest in relation to this study.
Figures
Similar articles
-
The Mre11/Rad50/Nbs1 complex plays an important role in the prevention of DNA rereplication in mammalian cells.J Biol Chem. 2007 Nov 2;282(44):32243-55. doi: 10.1074/jbc.M705486200. Epub 2007 Aug 22. J Biol Chem. 2007. PMID: 17715134
-
Breast cancer risk is associated with the genes encoding the DNA double-strand break repair Mre11/Rad50/Nbs1 complex.Cancer Epidemiol Biomarkers Prev. 2007 Oct;16(10):2024-32. doi: 10.1158/1055-9965.EPI-07-0116. Cancer Epidemiol Biomarkers Prev. 2007. PMID: 17932350
-
Mre11-Rad50-Nbs1 is a keystone complex connecting DNA repair machinery, double-strand break signaling, and the chromatin template.Biochem Cell Biol. 2007 Aug;85(4):509-20. doi: 10.1139/O07-069. Biochem Cell Biol. 2007. PMID: 17713585 Review.
-
Reduced levels of MRE11 cause disease phenotypes distinct from ataxia telangiectasia-like disorder.Hum Mol Genet. 2024 Sep 3;33(18):1605-1617. doi: 10.1093/hmg/ddae101. Hum Mol Genet. 2024. PMID: 38888340 Free PMC article.
-
Pharmacotherapy for smoking cessation: effects by subgroup defined by genetically informed biomarkers.Cochrane Database Syst Rev. 2017 Sep 8;9(9):CD011823. doi: 10.1002/14651858.CD011823.pub2. Cochrane Database Syst Rev. 2017. Retraction in: Cochrane Database Syst Rev. 2021 Nov 30;11:CD011823. doi: 10.1002/14651858.CD011823.pub3. PMID: 28884473 Free PMC article. Retracted.
References
-
- Taiwan Ministry of Health and Welfare Clinical Trial and Research Center of Excellence Cancer Registration Annual Report. Available at: https://www.hpa.gov.tw/Pages/List.aspx?nodeid=269. [Last accessed on March 25, 2025]
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical
Research Materials
Miscellaneous