田纳西州孟菲斯市非裔美国女性UGT1A1*28启动子多态性的流行与乳腺癌风险

Alana Smith, C. Cropp, G. Vidal, Elizabeth K Pritchard, Jennifer B. Cordero, Claire L. Simpson, A. Starlard-Davenport
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引用次数: 3

摘要

udp -葡萄糖醛酸糖基转移酶1A1 (UGT1A1)的遗传变异与非洲血统妇女乳腺癌风险增加有关。UGT1A1*28启动子多态性的特征是TATA box序列中存在7个TA重复序列,导致UGT1A1基因表达和酶活性降低。在这项研究中,我们调查了田纳西州孟菲斯市非裔美国人(AA)女性UGT1A1*28多态性与乳腺癌风险之间的关系,孟菲斯市是非裔美国人女性乳腺癌死亡率较高。在2016年6月至2017年6月期间收集了352名AA女性的唾液,其中包括乳腺癌患者(n=82)和对照组(n=270)。分离DNA并测序UGT1A1*28多态性。UGT1A1低活性等位基因(TA)7/8重复基因型与5/5、5/6和6/6重复基因型的比值比为1.46 [95% CI, 0.65-3.31;P = 0.36]和1.10 (95% CI, 0.52-2.38;P = 0.79)。TCGA RNA-seq数据的进一步分析显示,与非西班牙裔白人女性雌激素受体(ER)阴性乳腺癌患者相比,来自AA的雌激素受体(ER)阴性乳腺癌患者的UGT1A1 mRNA显著降低。需要更大规模的流行病学研究来确定UGT1A1*28多态性对AA女性乳腺癌风险的功能影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Prevalence of the UGT1A1*28 promoter polymorphism and breast cancer risk among African American women in Memphis, TN.
Inherited variations in UDP-glucuronosyltransferase 1A1 (UGT1A1) are associated with an increased breast cancer risk in women of African ancestry. The UGT1A1*28 promoter polymorphism is characterized by the presence of 7 TA repeats in the TATA box sequence and results in reduced UGT1A1 gene expression and enzymatic activity. In this study, we investigated associations between the UGT1A1*28 polymorphism and breast cancer risk among African American (AA) women in Memphis, Tennessee, a city with increased breast cancer mortality rates among AA women. Saliva was collected from 352 AA women, including breast cancer cases (n=82) and controls (n=270) between June 2016 to June 2017. DNA was isolated and sequenced for the UGT1A1*28 polymorphism. The odds ratio for cases with the low UGT1A1 activity alleles (TA)7/8 repeat genotypes versus 5/5, 5/6, and 6/6 genotypes was 1.46 [95% CI, 0.65-3.31; P = 0.36] in premenopausal women and 1.10 (95% CI, 0.52-2.38; P = 0.79) in postmenopausal women. Further analysis of TCGA RNA-seq data showed that UGT1A1 mRNA was significantly lower among estrogen receptor (ER)-negative breast cancers from AA as compared to non-Hispanic white women with ER-negative breast cancer. Larger epidemiological studies are needed to determine the functional consequence of the UGT1A1*28 polymorphism on breast cancer risk in AA women.
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