Environmental carcinogens often induce specific mutations in the p53 gene, apparent in tumors. The relation between aflatoxin B1(AFB1)-related hepatocellular carcinomas (HCCs) and hot spot at codon 249 of the p53 gene has received a great deal of attention, but its significance is still controversia
Polymorphism of XRCC1 and the frequency of mutation in codon 249 of the p53 gene in hepatocellular carcinoma among guangxi population, China
β Scribed by Xi Dai Long; Yun Ma; Hong Dong Huang; Jin Guang Yao; De Ying Qu; Yun Long Lu
- Publisher
- John Wiley and Sons
- Year
- 2008
- Tongue
- English
- Weight
- 77 KB
- Volume
- 47
- Category
- Article
- ISSN
- 0899-1987
- DOI
- 10.1002/mc.20384
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β¦ Synopsis
Abstract
In hepatocellular carcinoma (HCC), hotspot mutation in codon 249 of the __p__53 gene has been associated with exposure to aflatoxin B1 (AFB1). While the polymorphism of DNA repair gene Xβray repair crossβcomplementary group 1 (XRCC1) Arg399Gln may be related with AFB1βDNA adducts and gene mutations. Five hundred one HCCs were included in this study to investigate the role of the XRCC1 codon 399 polymorphism on hotspot mutation in codon 249 of the __p__53 gene. The genotypes of XRCC1 codon 399 and __p__53 codon 249 were examined by PCRβRFLP. The HCC patients with XRCC1 genotypes with 399 Gln (namely: XRCC1βAG/GG) exhibited a significantly higher frequency of the __p__53 hotspot mutations in codon 249 than those with the wildβtype homozygote of XRCC1 [namely: XRCC1βAA, adjusted odds ratio (OR)β=β6.77, 95% confidence interval (CI)β=β4.34β10.57]. Compared with those individuals who did express XRCC1βAA as reference (ORβ=β1), moreover, individuals featuring XRCC1βAG/GG and AFB1βDNA adducts did experience a significantly greater frequency of the hotspot mutation in codon 249 of the __p__53 gene (adjusted ORβ=β28.37, 95% CIβ=β13.19β61.02, Pβ<β0.01). This study suggests that the XRCC1 Arg399Gln polymorphism and AFB1βDNA adducts are associated with the increased frequency of the __p__53 mutations in codon 249. Β© 2007 WileyβLiss, Inc.
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