Suppr超能文献

谷胱甘肽S-转移酶M1(缺失/存在)、谷胱甘肽S-转移酶P1(Ile105Val)和P53(Arg72Pro)基因多态性与乳腺癌风险的关系:来自印度南部的一项病例对照研究。

Role of GSTM1 (Null/Present), GSTP1 (Ile105Val) and P53 (Arg72Pro) genetic polymorphisms and the risk of breast cancer: a case control study from South India.

作者信息

Samson Mani, Swaminathan Rajaraman, Rama Ranganathan, Sridevi Veluswami, Nancy Karunakaran Nirmala, Rajkumar Thangarajan

机构信息

Department of Molecular Oncology, Cancer Institute (WIA), Adyar, Chennai, India.

出版信息

Asian Pac J Cancer Prev. 2007 Apr-Jun;8(2):253-7.

Abstract

The present study was undertaken to examine the frequencies of GSTM1 (Null/Present), GSTP1 (Ile105Val) and p53 (Arg72Pro) genotypes and their relations to breast cancer susceptibility in South Indian women. This case - control study involved 250 consecutive breast cancer cases and 500 healthy controls matched in five-year age categories in the ratio of 1:2. Genotyping was performed by PCR for GSTM1, Real-Time Allelic discrimination assay for GSTP1 and PCR-CTPP for p53. Odds ratios (ORs) and 95% confidence intervals (CIs) were calculated using conditional logistic regression after adjusting for the known risk factors for breast cancer. The frequencies for the GSTM1 Null genotype were 26% in the cases and 22% in the controls; for GSTP1 Ile/Ile, Ile/Val, Val/Val the frequencies were 46.6%, 41.9% and 11.5%, respectively, in cases and 46.0%, 43.8% and 10.2% in controls; for p53 Arg/Arg, Arg/Pro & Pro/Pro the frequencies were 26.4%, 50.0% and 23.6% in cases and 27.0%, 44.8% and 28.2% in controls. A nonsignificant elevation in breast cancer risk was observed among women who had the GSTM1 Null genotype (OR=1.24; 95% CI=0.83-1.84), the p53 Arg/Arg genotype (OR=1.28; 95% CI=0.81-2.03) and the Pro/Arg genotype (OR=1.49; 95% CI=0.99-2.25), and the GSTP1 Val/Val genotype (OR=1.1; 95% CI=0.64-1.91).

摘要

本研究旨在检测南印度女性中GSTM1(缺失/存在)、GSTP1(Ile105Val)和p53(Arg72Pro)基因的基因型频率及其与乳腺癌易感性的关系。这项病例对照研究纳入了250例连续的乳腺癌病例和500名健康对照,按5岁年龄组匹配,比例为1:2。采用聚合酶链反应(PCR)对GSTM1进行基因分型,采用实时等位基因鉴别分析对GSTP1进行基因分型,采用PCR-CTPP对p53进行基因分型。在对已知的乳腺癌风险因素进行校正后,使用条件逻辑回归计算比值比(OR)和95%置信区间(CI)。GSTM1缺失基因型的频率在病例组中为26%,在对照组中为22%;GSTP1 Ile/Ile、Ile/Val、Val/Val基因型的频率在病例组中分别为46.6%、41.9%和11.5%,在对照组中分别为46.0%、43.8%和10.2%;p53 Arg/Arg、Arg/Pro和Pro/Pro基因型的频率在病例组中分别为26.4%、50.0%和23.6%,在对照组中分别为27.0%、44.8%和28.2%。在具有GSTM1缺失基因型(OR=1.24;95%CI=0.83-1.84)、p53 Arg/Arg基因型(OR=1.28;95%CI=0.81-2.03)和Pro/Arg基因型(OR=1.49;95%CI=0.99-2.25)以及GSTP1 Val/Val基因型(OR=1.1;95%CI=0.64-1.91)的女性中,观察到乳腺癌风险有非显著性升高。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验