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GSTP1 I105V Polymorphism and Susceptibility to Colorectal Cancer in Kashmiri Population

机译:克什米尔人口中的GSTP1 I105V多态性和对结直肠癌的易感性

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摘要

The glutathione S-transferase (GST) enzyme encoded by the GSTP1 gene is one of the critical enzymes involved in detoxification of carcinogens. The substitution of isoleucine to valine residue at position 105 of the GSTP1 protein results in decreased enzyme activity and hence less capability of effective detoxification. Hence, we investigated the role of GSTP1 I105V polymorphism in modulating the risk of colorectal cancer (CRC) associated in a Kashmiri population. We designed a case-control study in which 86 CRC cases were studied for GSTP1 I105V polymorphism against 160 controls taken from the general population employing the polymerase chain reaction-restriction length fragment polymorphism technique. There was no significant association between GSTP1 I105V genotypes and the disease, but the Val/Val genotype was associated with an increased risk with some clinicopathological parameters (odds ratio = 1.5; 95% confidence interval = 0.55-4.57). This study suggests that the GSTP1 I105V polymorphism may modulate CRC risk in the Kashmiri population.
机译:GSTP1基因编码的谷胱甘肽S-转移酶(GST)是致癌物解毒的关键酶之一。异亮氨酸被GSTP1蛋白105位上的缬氨酸残基取代导致酶活性降低,因此有效排毒的能力降低。因此,我们调查了GSTP1 I105V多态性在调节克什米尔人群中与结直肠癌(CRC)相关的风险中的作用。我们设计了一个病例对照研究,其中使用聚合酶链反应-限制性酶切长度片段多态性技术,针对来自普通人群的160例对照研究了GSTP1 I105V多态性的CRC病例。 GSTP1 I105V基因型与疾病之间无显着相关性,但Val / Val基因型与某些临床病理参数的风险增加相关(奇数比= 1.5; 95%置信区间= 0.55-4.57)。这项研究表明,GSTP1 I105V多态性可能会调节克什米尔居民中的CRC风险。

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