Cargando…

Polymorphisms of XRCC1 genes and risk of nasopharyngeal carcinoma in the Cantonese population

BACKGROUND: Nasopharyngeal carcinoma (NPC) is one of the most common cancers in southern China. In addition to environmental factors such as Epstein-Barr virus infection and diet, genetic susceptibility has been reported to play a key role in the development of this disease. The x-ray repair cross-c...

Descripción completa

Detalles Bibliográficos
Autores principales: Cao, Yun, Miao, Xiao-Ping, Huang, Ma-Yan, Deng, Ling, Hu, Li-Fu, Ernberg, Ingemar, Zeng, Yi-Xin, Lin, Dong-Xin, Shao, Jian-Yong
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1550725/
https://www.ncbi.nlm.nih.gov/pubmed/16796765
http://dx.doi.org/10.1186/1471-2407-6-167
_version_ 1782129270772989952
author Cao, Yun
Miao, Xiao-Ping
Huang, Ma-Yan
Deng, Ling
Hu, Li-Fu
Ernberg, Ingemar
Zeng, Yi-Xin
Lin, Dong-Xin
Shao, Jian-Yong
author_facet Cao, Yun
Miao, Xiao-Ping
Huang, Ma-Yan
Deng, Ling
Hu, Li-Fu
Ernberg, Ingemar
Zeng, Yi-Xin
Lin, Dong-Xin
Shao, Jian-Yong
author_sort Cao, Yun
collection PubMed
description BACKGROUND: Nasopharyngeal carcinoma (NPC) is one of the most common cancers in southern China. In addition to environmental factors such as Epstein-Barr virus infection and diet, genetic susceptibility has been reported to play a key role in the development of this disease. The x-ray repair cross-complementing group 1 (XRCC1) gene is important in DNA base excision repair. We hypothesized that two common single nucleotide polymorphisms of XRCC1 (codons 194 Arg→Trp and 399 Arg→Gln) are related to the risk of NPC and interact with tobacco smoking. METHODS: We sought to determine whether these genetic variants of the XRCC1 gene were associated with the risk of NPC among the Cantonese population in a hospital-based case control study using polymerase chain reaction-restriction fragment length polymorphism analysis. We conducted this study in 462 NPC patients and 511 healthy controls. RESULTS: After adjustment for sex and age, we found a reduced risk of developing NPC in individuals with the Trp194Trp genotype (OR = 0.48; 95% CI, 0.27–0.86) and the Arg194Trp genotype (OR = 0.79; 95% CI, 0.60–1.05) compared with those with the Arg194Arg genotype. Compared with those with the Arg399Arg genotype, the risk for NPC was not significantly different in individuals with the Arg399Gln genotype (OR = 0.82; 95% CI, 0.62–1.08) and the Gln399Gln genotype (OR = 1.20; 95% CI, 0.69–2.06). Further analyses stratified by gender and smoking status revealed a significantly reduced risk of NPC among males (OR = 0.32; 95% CI, 0.14–0.70) and smokers (OR = 0.34; 95% CI, 0.14–0.82) carrying the XRCC1 194Trp/Trp genotype compared with those carrying the Arg/Arg genotype. No association was observed between Arg399Gln variant genotypes and the risk of NPC combined with smoking and gender. CONCLUSION: Our findings suggest that the XRCC1 Trp194Trp variant genotype is associated with a reduced risk of developing NPC in Cantonese population, particularly in males and smokers. Larger studies are needed to confirm our findings and unravel the underlying mechanisms.
format Text
id pubmed-1550725
institution National Center for Biotechnology Information
language English
publishDate 2006
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-15507252006-08-19 Polymorphisms of XRCC1 genes and risk of nasopharyngeal carcinoma in the Cantonese population Cao, Yun Miao, Xiao-Ping Huang, Ma-Yan Deng, Ling Hu, Li-Fu Ernberg, Ingemar Zeng, Yi-Xin Lin, Dong-Xin Shao, Jian-Yong BMC Cancer Research Article BACKGROUND: Nasopharyngeal carcinoma (NPC) is one of the most common cancers in southern China. In addition to environmental factors such as Epstein-Barr virus infection and diet, genetic susceptibility has been reported to play a key role in the development of this disease. The x-ray repair cross-complementing group 1 (XRCC1) gene is important in DNA base excision repair. We hypothesized that two common single nucleotide polymorphisms of XRCC1 (codons 194 Arg→Trp and 399 Arg→Gln) are related to the risk of NPC and interact with tobacco smoking. METHODS: We sought to determine whether these genetic variants of the XRCC1 gene were associated with the risk of NPC among the Cantonese population in a hospital-based case control study using polymerase chain reaction-restriction fragment length polymorphism analysis. We conducted this study in 462 NPC patients and 511 healthy controls. RESULTS: After adjustment for sex and age, we found a reduced risk of developing NPC in individuals with the Trp194Trp genotype (OR = 0.48; 95% CI, 0.27–0.86) and the Arg194Trp genotype (OR = 0.79; 95% CI, 0.60–1.05) compared with those with the Arg194Arg genotype. Compared with those with the Arg399Arg genotype, the risk for NPC was not significantly different in individuals with the Arg399Gln genotype (OR = 0.82; 95% CI, 0.62–1.08) and the Gln399Gln genotype (OR = 1.20; 95% CI, 0.69–2.06). Further analyses stratified by gender and smoking status revealed a significantly reduced risk of NPC among males (OR = 0.32; 95% CI, 0.14–0.70) and smokers (OR = 0.34; 95% CI, 0.14–0.82) carrying the XRCC1 194Trp/Trp genotype compared with those carrying the Arg/Arg genotype. No association was observed between Arg399Gln variant genotypes and the risk of NPC combined with smoking and gender. CONCLUSION: Our findings suggest that the XRCC1 Trp194Trp variant genotype is associated with a reduced risk of developing NPC in Cantonese population, particularly in males and smokers. Larger studies are needed to confirm our findings and unravel the underlying mechanisms. BioMed Central 2006-06-26 /pmc/articles/PMC1550725/ /pubmed/16796765 http://dx.doi.org/10.1186/1471-2407-6-167 Text en Copyright © 2006 Cao et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Cao, Yun
Miao, Xiao-Ping
Huang, Ma-Yan
Deng, Ling
Hu, Li-Fu
Ernberg, Ingemar
Zeng, Yi-Xin
Lin, Dong-Xin
Shao, Jian-Yong
Polymorphisms of XRCC1 genes and risk of nasopharyngeal carcinoma in the Cantonese population
title Polymorphisms of XRCC1 genes and risk of nasopharyngeal carcinoma in the Cantonese population
title_full Polymorphisms of XRCC1 genes and risk of nasopharyngeal carcinoma in the Cantonese population
title_fullStr Polymorphisms of XRCC1 genes and risk of nasopharyngeal carcinoma in the Cantonese population
title_full_unstemmed Polymorphisms of XRCC1 genes and risk of nasopharyngeal carcinoma in the Cantonese population
title_short Polymorphisms of XRCC1 genes and risk of nasopharyngeal carcinoma in the Cantonese population
title_sort polymorphisms of xrcc1 genes and risk of nasopharyngeal carcinoma in the cantonese population
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1550725/
https://www.ncbi.nlm.nih.gov/pubmed/16796765
http://dx.doi.org/10.1186/1471-2407-6-167
work_keys_str_mv AT caoyun polymorphismsofxrcc1genesandriskofnasopharyngealcarcinomainthecantonesepopulation
AT miaoxiaoping polymorphismsofxrcc1genesandriskofnasopharyngealcarcinomainthecantonesepopulation
AT huangmayan polymorphismsofxrcc1genesandriskofnasopharyngealcarcinomainthecantonesepopulation
AT dengling polymorphismsofxrcc1genesandriskofnasopharyngealcarcinomainthecantonesepopulation
AT hulifu polymorphismsofxrcc1genesandriskofnasopharyngealcarcinomainthecantonesepopulation
AT ernbergingemar polymorphismsofxrcc1genesandriskofnasopharyngealcarcinomainthecantonesepopulation
AT zengyixin polymorphismsofxrcc1genesandriskofnasopharyngealcarcinomainthecantonesepopulation
AT lindongxin polymorphismsofxrcc1genesandriskofnasopharyngealcarcinomainthecantonesepopulation
AT shaojianyong polymorphismsofxrcc1genesandriskofnasopharyngealcarcinomainthecantonesepopulation