Liver Cancer
Copyright ©The Author(s) 2002. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Gastroenterol. Jun 15, 2002; 8(3): 480-482
Published online Jun 15, 2002. doi: 10.3748/wjg.v8.i3.480
The point mutation of p53 gene exon7 in hepatocellular carcinoma from Anhui Province, a non HCC prevalent area in China
Hu Liu, Yuan Wang, Qing Zhou, Shu-Yu Gui, Xu Li
Hu Liu, Yuan Wang, Qing Zhou, Laboratory of Molecular Biology and Department of Biochemistry, Anhui Medical University, Hefe 230032i, Anhui Province, China
Shu-Yu Gui, Department of Respiratory Disease, the First Affiliated Hospital of Anhui Medical University, Hefei 230022, Anhui Province, China
Xu Li, Department of Infectious Disease, the First Affiliated Hospital of Anhui Medical University, Hefei 230022, Anhui Province, China
Author contributions: All authors contributed equally to the work.
Supported by the Natural Science Foundation of Anhui Province, No. 99044312 (WY) and No. 9741006 (LX) and Natural Science Foundation of Anhui Educational Commission, No. JL-97-077 (WY).
Correspondence to: Yuan Wang, Laboratory of Molecular Biology, Anhui Medical University, Hefei 230032, Anhui Province, China. wangyuan@mail.hf.ah.cn
Telephone: +86-551-5161140
Received: December 20, 2001
Revised: January 5, 2002
Accepted: January 24, 2002
Published online: June 15, 2002
Abstract

AIM: In hepatocellular carcinoma (HCC) prevalent areas of China, the point mutation of p53 exon7 is highly correlated with Hepatitis B virus (HBV) infection and aflatoxin B intake. While in non-HCC-prevalent areas of China, these factors are not so important in the etiology of HCC. Therefore, the point mutation of p53 exon7 may also be different than that in HCC-prevalent areas of China. The aim of this study is to investigate the status and carcinogenic role of the point mutation of p53 gene exon7 in hepatocellular carcinoma from Anhui Province, a non-HCC-prevalent area in China.

METHODS: PCR, PCR-SSCP and PCR-RFLP were applied to analyze the homozygous deletion and point mutation of p53 exon7 in HCC samples from Anhui, which were confirmed by DNA sequencing and Genbank comparison.

RESULTS: In the 38 samples of hepatocellular carcinoma, no homozygous deletion of p53 exon7 was detected and point mutations of p53 exon7 were found in 4 cases, which were found to be heterozygous mutation of codon 249 with a mutation rate of 10.53% (4/38). The third base mutation (GiúT) of p53 codon 249 was found by DNA sequencing and Genbank comparison.

CONCLUSION: The incidence of point mutation of p53 codon 249 is lower in hepatocellular carcinoma and the heterozygous mutation of p53 exon7 found in these patients only indicate that they have genetic susceptibility to HCC. p53 codon 249 is a hotspot of p53 exon7 point mutation, suggesting that the point mutation of p53 exon 7 may not play a major role in the carcinogenesis of HCC in Anhui Province, a non-HCC-prevalent area in China.

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