The study on the relationship between XRCC1 gene polymorphisms and the susceptibility of colorectal cancer
10.3760/cma.j.issn.0254-1432.2011.07.006
- VernacularTitle:X线损伤交叉互补基因1多态性与结直肠癌易感性研究
- Author:
Chan ZHU
;
Ying ZHANG
;
Qian BAO
;
Yongfei XU
;
Lili QU
;
Zhipeng TANG
;
Fuliang TIAN
;
Shukui WANG
- Publication Type:Journal Article
- Keywords:
Colorectal neoplasms;
Polymorphism,genetic;
DNA repairnzynes;
Alleles;
Genetic predisposition to disease
- From:
Chinese Journal of Digestion
2011;31(7):450-454
- CountryChina
- Language:Chinese
-
Abstract:
Objective To investigate the correlation between three gene locus polymorphisms of X-ray repair cross-complementary protein 1 (XRCC1) exon (Arg194Trp, Arg280His and Arg399Gln) and the risk of colorectal cancer (CRC). Methods A case-control study was performed in 250 CRC patients (case group, 128 colon cancer patients and 122 rectal cancer patients) and 213 healthy individuals (control group). The three gene locus polymorphism of XRCC1 was tested by polymerase chain reaction and restriction fragment length polymorphism (PCR-RFLP) method. The genotype distribution and allele frequency of each locus was analyzed with SPSS 10.0 software. Results There was no significant difference in allele frequency of XRCC1 at 194 and 399 loci (P > 0.05). However, the 280 Arg/His allele frequency of XRCC1 was higher in case group than that in control group (OR=1.66,95%CI:1.01~2.73,P=0.047). The 280Arg/His allele frequency was higher in rectal cancer group than that in control group (OR =1.82,95%CI:1.02~3.27). The frequency of 280His allele (Arg280His and His280His) was higher in case group than that in control group (OR=1.85,95%CI:1.06~3.22). However, it was a relative low risk factor of colon cancer and there was no significant difference between colon cancer group and control group (OR=1.85, 95%CI:1.06~3.22). Conclusions There was no correlation between XRCC1 Arg194Trp and Arg399Gln polymorpohisms and the risk of CRC. However, 280Arg/His genotype may increase the risk of CRC, and 280His allele is a risk factor of rectal cancer.
