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乳腺癌中UDP-葡萄糖醛酸基转移酶(UGT1A1)启动子多态性及其基因表达在种族、疾病分期和绝经状态方面的特征分析

Characterization of UDP-glucuronosyltransferase (UGT1A1) Promoter Polymorphisms and Gene Expression on Ethnicity, Stage of Disease, and Menopausal Status in Breast Cancer.

作者信息

Starlard-Davenport Athena, Word Beverly R, Lyn-Cook Beverly

机构信息

Office of the Associate Director for Regulatory Activities, National Center for Toxicological Research, Jefferson, AR 72079, USA.

出版信息

J Drug Metab Toxicol. 2012;2012(Suppl 4). doi: 10.4172/2157-7609.S4-001. Epub 2012 Mar 19.

Abstract

Estrogen metabolism, catalyzed by UGTs, is a major drug-metabolic pathway that results in inactivation of estrogens and their metabolites. Alterations in UGTs involved in estrogen metabolism, has been suggested to play a role in breast cancer risk. The purpose of this study was to: 1) compare the mRNA expression levels of UGTs involved in estrogen metabolism in human breast tissues from women; 2) compare UGT1A1 mRNA expression to tumor stage, ethnicity, and menopausal status in a group of human breast tumors and normal breast tissues, and 3) investigate the association between variations in the number of TA repeats in the promoter region of UGT1A1 to gene expression. Quantification of UGT mRNA in breast tissues revealed that UGT1A4, UGT1A10, and UGT2B7 mRNA levels were decreased in breast cancers as compared to normal breast tissues. UGT1A1 mRNA levels were also significantly decreased in breast cancers as compared to normal breast tissues (Tumor: 0.5 ± 0.2; Normal: 4.1 ± 1.3, = 0.0006). UGT1A1 mRNA down-regulation was strongly correlated with postmenopausal status in breast cancer versus controls ( = 0.04). In all the UGT1A1 genotypes observed in our study, the mean mRNA levels was significantly decreased among breast cancer cases as compared to controls for ( = 0.004), ( = 0.03) and ( = 0.06). Our findings demonstrate that further investigations are necessary to determine the role of UGT1A1 in breast carcinogenesis.

摘要

由尿苷二磷酸葡萄糖醛酸基转移酶(UGTs)催化的雌激素代谢是导致雌激素及其代谢产物失活的主要药物代谢途径。参与雌激素代谢的UGTs的改变被认为在乳腺癌风险中起作用。本研究的目的是:1)比较女性人乳腺组织中参与雌激素代谢的UGTs的mRNA表达水平;2)在一组人乳腺肿瘤和正常乳腺组织中比较UGT1A1 mRNA表达与肿瘤分期、种族和绝经状态,以及3)研究UGT1A1启动子区域TA重复序列数量的变异与基因表达之间的关联。乳腺组织中UGT mRNA的定量分析显示,与正常乳腺组织相比,乳腺癌中UGT1A4、UGT1A10和UGT2B7 mRNA水平降低。与正常乳腺组织相比,乳腺癌中UGT1A1 mRNA水平也显著降低(肿瘤:0.5±0.2;正常:4.1±1.3,P = 0.0006)。与对照组相比,乳腺癌中UGT1A1 mRNA下调与绝经后状态密切相关(P = 0.04)。在我们研究中观察到的所有UGT1A1基因型中,与对照组相比,乳腺癌病例中的平均mRNA水平在P = 0.004、P = 0.03和P = 0.06时显著降低。我们的研究结果表明,有必要进一步研究以确定UGT1A1在乳腺癌发生中的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d608/6195800/df6ca6de1e2b/nihms-991696-f0001.jpg

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