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约旦女性中谷胱甘肽S-转移酶M1、谷胱甘肽S-转移酶T1和谷胱甘肽S-转移酶P1基因多态性与乳腺癌的关联

Association Of GSTM1, GSTT1 And GSTP1 Polymorphisms With Breast Cancer Among Jordanian Women.

作者信息

Al-Eitan Laith N, Rababa'h Doaa M, Alghamdi Mansour A, Khasawneh Rame H

机构信息

Department of Applied Biological Sciences, Jordan University of Science and Technology, Irbid 22110, Jordan.

Department of Biotechnology and Genetic Engineering, Jordan University of Science and Technology, Irbid 22110, Jordan.

出版信息

Onco Targets Ther. 2019 Sep 20;12:7757-7765. doi: 10.2147/OTT.S207255. eCollection 2019.

Abstract

PURPOSE

Genetic predisposition to disease has become one of the most investigated risk factors in recent years, and breast cancer (BC) is no exception. In this study, we investigated specific genetic variants of three candidate genes belonging to the glutathione-S-transferase superfamily that have been implicated in increased risk of cancers.

MATERIALS AND METHODS

This case-control study comprised 241 Jordanian women who were diagnosed with BC in addition to 219 matched controls. Gel electrophoresis of PCR products was used to visualize and genotype both the and genes, while PCR-RFLP was employed to genotype the rs1695 of the gene.

RESULTS

Our findings did not reveal any correlation between the investigated polymorphisms of GST genes and BC risk among Jordanian women. Otherwise, the combination of entire gene deletion and (GG) genotype of polymorphism (rs1695) was significantly associated with BC with p-value <0.05 (i.e. p-value was not significant after correcting for multiple comparison).

CONCLUSION

We suggest that the interaction between polymorphism and rs1695 of may influence BC development and progression among Jordanian women. More epidemiological studies are needed to provide a baseline for the underlying role of GSTs polymorphisms in tumorigenesis.

摘要

目的

疾病的遗传易感性已成为近年来研究最多的风险因素之一,乳腺癌(BC)也不例外。在本研究中,我们调查了谷胱甘肽-S-转移酶超家族中三个候选基因的特定遗传变异,这些变异与癌症风险增加有关。

材料与方法

本病例对照研究包括241名被诊断为乳腺癌的约旦女性以及219名匹配的对照。PCR产物的凝胶电泳用于可视化和基因分型GSTM1和GSTT1基因,而PCR-RFLP用于对GSTP1基因的rs1695进行基因分型。

结果

我们的研究结果未揭示约旦女性中GST基因的研究多态性与乳腺癌风险之间的任何相关性。否则,GSTM1全基因缺失与GSTP1多态性(rs1695)的(GG)基因型的组合与乳腺癌显著相关,p值<0.05(即在校正多重比较后p值不显著)。

结论

我们认为GSTM1多态性与GSTP1的rs1695之间的相互作用可能影响约旦女性乳腺癌的发生和发展。需要更多的流行病学研究来为GSTs多态性在肿瘤发生中的潜在作用提供基线。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/97e3/6760517/82f5168baf2e/OTT-12-7757-g0001.jpg

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