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肝癌组织GSTM1基因的缺失突变
引用本文:边建超,沈福民,王金兵,陈公超,张宝初,吴燕.肝癌组织GSTM1基因的缺失突变[J].中华医学遗传学杂志,1999,16(3):171-173.
作者姓名:边建超  沈福民  王金兵  陈公超  张宝初  吴燕
作者单位:1. 200032,上海医科大学流行病学教研室
2. 江苏省启东肝癌防治研究所
3. 海门市卫生防疫站
摘    要:目的探讨在肝癌发生的过程中谷胱甘肽S-转移酶M1基因(glutathioneS-transferase,GSTM1)基因是否发生缺失突变。方法应用PCR技术检测46对肝癌组织和癌周肝组织的GSTM1基因型。结果肝癌组织GSTM1空白基因型的频率为78.26%,癌周肝组织则为65.22%(P<0.05)。6例肝癌组织的GSTM1空白基因型由癌周肝组织的非空白基因型转变而成,占13.04%。根据Hardy-Weinberg定律,推出GSTM1基因的缺失突变率为38.89%。结论在肝癌发生的过程中,GSTM1基因发生了缺失突变。

关 键 词:肝癌  谷胱甘肽S-转移酶M1基因  缺失突变

The mutation of deletion for glutathione S-transferase M1 gene in the tissue of hepatocellular carcinoma
BIAN Jianchao,SHEN Fumin,WANG Jinbing,CHEN Gongchao,ZHANG Baochu,WU Yan.The mutation of deletion for glutathione S-transferase M1 gene in the tissue of hepatocellular carcinoma[J].Chinese Journal of Medical Genetics,1999,16(3):171-173.
Authors:BIAN Jianchao  SHEN Fumin  WANG Jinbing  CHEN Gongchao  ZHANG Baochu  WU Yan
Institution:Department of Epidemiology, Shanghai Medical University, Shanghai, 200032 P.R.China. jcbian@shmu.edu.cn
Abstract:Objective To study whether the mutation of deletion for glutathione Stransferase M1(GSTM1) gene occurred during the development of hepatocellular carcinoma(HCC). Methods The genotypes of GSTM1 of 46 pairs of HCC tissue and the noncancerous liver tissue were detected by polymerase chain reaction(PCR). Results The frequency of GSTM1 null genotype for HCC tissue was 78.26%, but 65.22% for the noncancerous liver tissue (P<0.05).The GSTM1 null genotypes of 6 HCC tissue were transformed from the nonnull genotypes of the noncancerous liver tissue. According to HardyWeinberg law, the rate of deletion mutation for GSTM1 gene was inferred to be 38.89%. Conclusion The results suggested that the mutation of deletion for GSTM1 gene had occurred during the development of HCC.
Keywords:HepatocarcinomaGSTM1 geneDeletion
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