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采用基于聚合酶链反应的方法在中国健康人群中快速检测谷胱甘肽S-转移酶基因的常见突变

Rapid determination of common mutations in glutathione S-transferase gene by PCR-based methods in healthy Chinese.

作者信息

Zhong Shi-long, Zhou Shufeng, Chen Xiao, Huang Min

机构信息

Institute of Clinical Pharmacology, School of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou 510080, People's Republic of China.

出版信息

Clin Chim Acta. 2006 Feb;364(1-2):205-8. doi: 10.1016/j.cccn.2005.06.021. Epub 2005 Aug 10.

Abstract

BACKGROUND

The glutathione S-transferase (GST) superfamily comprises multiple isozymes with compelling evidence of functional polymorphisms in various ethnic groups. All these mutations, in particular those in class mu, pi and theta GST, are likely to contribute to interindividual differences in responses to xenobiotics including response to chemotherapy and associated with altered disease. The frequency of common GST mutations in Uygur Chinese is unknown. We investigated the common mutations of GSTM1, GSTT1, and GSTP1 in Uygur (N=154) Chinese and compare with Han Chinese (N=196).

METHOD

GSTM1 and GSTT1 polymorphisms were analyzed by multiplexed PCR, and GSTP1 polymorphism was detected by PCR-based restriction fragment length polymorphism (RFLP) analysis.

RESULTS

GSTM1 null genotype was found in 53.2% Uygur Chinese, which was close to that in Han Chinese (56.1%) (P=0.592). A significantly lower frequency (P<0.05) of GSTT1 null genotype in Uygur Chinese (26.6%) was observed compared with Han Chinese (50.0%). Uygur Chinese exhibited a GSTP1 genotype distribution of 51.3% I/I, 40.2% I/V and 8.4% V/V, which was different from that in Han Chinese (60.7% I/I, 35.2% I/V and 4.1% V/V).

CONCLUSIONS

There is marked ethnic difference in the frequency of common GSTT1 and GSTP1 mutation, but not GSTM1 mutation, between Uygur and Han Chinese.

摘要

背景

谷胱甘肽S-转移酶(GST)超家族由多种同工酶组成,有确凿证据表明其在不同种族中存在功能多态性。所有这些突变,尤其是μ、π和θ类GST中的突变,可能导致个体对外源化学物质反应的差异,包括对化疗的反应,并与疾病改变相关。维吾尔族中国人中常见GST突变的频率尚不清楚。我们调查了维吾尔族(N = 154)中国人中GSTM1、GSTT1和GSTP1的常见突变,并与汉族(N = 196)进行比较。

方法

通过多重PCR分析GSTM1和GSTT1多态性,通过基于PCR的限制性片段长度多态性(RFLP)分析检测GSTP1多态性。

结果

53.2%的维吾尔族中国人中发现GSTM1无效基因型,这与汉族(56.1%)相近(P = 0.592)。与汉族(50.0%)相比,维吾尔族中国人中GSTT1无效基因型的频率显著较低(P < 0.05)(26.6%)。维吾尔族中国人的GSTP1基因型分布为51.3% I/I、40.2% I/V和8.4% V/V,这与汉族(60.7% I/I、35.2% I/V和4.1% V/V)不同。

结论

维吾尔族和汉族之间,常见GSTT1和GSTP1突变的频率存在显著种族差异,但GSTM1突变不存在。

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