首页> 外文期刊>World Journal of Gastroenterology >Polymorphism of glutathione S-transferase mu 1 and theta 1 genes and hepatocellular carcinoma in southern Guangxi, China.
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Polymorphism of glutathione S-transferase mu 1 and theta 1 genes and hepatocellular carcinoma in southern Guangxi, China.

机译:广西南部谷胱甘肽S-转移酶mu 1和theta 1基因的多态性与肝细胞癌的关系。

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摘要

AIM: Glutathione S-transferase mu 1 (GSTM1) and theta 1 (GSTT1) genes are involved in the metabolism of a wide range of carcinogens, but deletions of the genes are commonly found in the population. The present study was undertaken to evaluate the association between GSTM1 and GSTT1 gene polymorphisms and hepatocellular carcinoma (HCC) risk. METHODS: The genetic polymorphisms were studied at an aflatoxin highly contaminated region in Guangxi, China. Polymerase chain reaction (PCR) technique was used to detect the presence or absence of the GSTM1 and GSTT1 genes in blood samples. The case group was composed of 181 patients of HCC identified by the pathologists and the control group was composed of 360 adults without any tumor. RESULTS: The frequencies of GSTM1 and GSTT1 null genotypes in the control were 47.8% and 42.7%, while those in the HCC group were 64.6% and 59.7%, respectively. The differences between HCC group and control group were very significant (P<0.01). GSTM1 and GSTT1 combined null genotypes in HCC group and control group were 38.2% and 18.5% respectively, and the difference was significant (P<0.05). CONCLUSION: The GSTM1 and GSTT1 null genotypes are associated with an increased risk of HCC in a special geographic environment. Combination of the two null genotypes in an individual is substantially increased twice the risk of HCC.
机译:目的:谷胱甘肽S-转移酶mu 1(GSTM1)和theta 1(GSTT1)基因参与多种致癌物的代谢,但是该基因的缺失在人群中很常见。本研究旨在评估GSTM1和GSTT1基因多态性与肝细胞癌(HCC)风险之间的关联。方法:在广西黄曲霉毒素高污染地区研究了遗传多态性。聚合酶链反应(PCR)技术用于检测血液样本中GSTM1和GSTT1基因的存在与否。病例组由病理学家鉴定的181例HCC患者组成,对照组由360例无肿瘤的成人组成。结果:对照组中GSTM1和GSTT1无效基因型的频率分别为47.8%和42.7%,而HCC组分别为64.6%和59.7%。 HCC组与对照组之间的差异非常显着(P <0.01)。 HCC组和对照组的GSTM1和GSTT1组合无效基因型分别为38.2%和18.5%,差异有统计学意义(P <0.05)。结论:在特殊地理环境中,GSTM1和GSTT1无效基因型与HCC风险增加有关。个体中两种无效基因型的组合大大增加了发生HCC风险的两倍。

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