Polymorphisms of XRCC1 gene and risk of gastric cardiac adenocarcinoma

39Citations
Citations of this article
15Readers
Mendeley users who have this article in their library.
Get full text

Abstract

X-ray repair cross complementing 1 (XRCC1) protein plays an important role in base excision repair. Single nucleotide polymorphisms (SNPs) in XRCC1 gene may affect DNA repairing ability and genetic susceptibility to cancer. This study was designed to investigate the correlation of XRCC1 Arg194Trp Arg280His and Arg399Gln SNPs with the risk of gastric cardiac adenocarcinoma (GCA). Genotypes were analyzed by polymerase chain reaction-restriction fragment length polymorphism assay in 455 patients with GCA and 650 age- and sex-matched controls. We did not find any significant difference in allele and genotype distributions of Arg194Trp Arg399Gln between the groups (P > 0.05). However, a significant increase in GCA risk was seen among smokers if they carried at least one XRCC1 280His (Arg280His + His280His ) genotype (odds ratio = 1.59, 95% confidence interval = 1.01-2.51) compared with smokers not carrying these genotype. Our results indicated that XRCC1 Arg194Trp and Arg 399 Gln SNPs might not be associated with the risk of GCA. However, smokers with His allele at codon 280 had a significantly increased risk of GCA. © 2009 International Society for Diseases of the Esophagus.

Cite

CITATION STYLE

APA

Yan, L., Yanan, D., Donglan, S., Na, W., Rongmiao, Z., & Zhifeng, C. (2009). Polymorphisms of XRCC1 gene and risk of gastric cardiac adenocarcinoma. Diseases of the Esophagus, 22(5), 396–401. https://doi.org/10.1111/j.1442-2050.2008.00912.x

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free