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Association Between BRCA Status and Triple-Negative Breast Cancer: A Meta-Analysis

机译:BRCA状态与三阴性乳腺癌之间的关联:一项荟萃分析

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摘要

Triple-negative breast cancer (TNBC) is a subtype of aggressive breast cancer and characterized by a lack of the expression of estrogen receptor, progesterone receptor and human epidermal growth factor receptor 2. BRCA genes are tumor-suppressor genes that are involved in DNA damage repair and mutations of BRCA genes may increase the risk of developing breast cancer and/or ovarian cancer due to defective DNA repair mechanisms. However, the relationship between BRCA status and TNBC needs to be further investigated and validated. The aim of this meta-analysis was to evaluate the association between BRCA status and TNBC. We systematically searched the electronic databases of MEDLINE (PubMed), Embase, and Cochrane Library to identify relevant publications from April, 1959 to November, 2017. The data from the studies were examined by a meta-analysis using STATA software to calculate the odds ratio (OR) with 95% confidence interval (CI) by fixed-effect and random-effect models. We identified 16 qualified studies from 527 publications with 46,870 breast cancer patients including 868 BRCA1 mutations (BRCA1Mut) carriers, 739 BRCA2 mutations (BRCA2Mut) carriers, and 45,263 non-carriers. The results showed that breast cancer patients with BRCA1Mut carriers were more likely to have TNBC than those of BRCA2Mut carriers (OR: 3.292; 95% CI: 2.773–3.909) or non-carriers (OR: 8.889; 95% CI: 6.925–11.410). Furthermore, high expression of nuclear grade and large tumor burden (>2 cm) were significantly more common in breast cancer patients with BRCA1Mut carriers than those of BRCA2Mut carriers (OR: 2.663; 95% CI: 1.731–4.097; P = 0.211) or non-carriers (OR: 1.577; 95% CI: 1.067–2.331; P = 0.157). The data suggest that breast cancer patients with BRCA1Mut are more likely to have TNBC, high nuclear grade, and larger tumor burden.
机译:三阴性乳腺癌(TNBC)是侵袭性乳腺癌的一种亚型,其特征是缺乏雌激素受体,孕激素受体和人类表皮生长因子受体2的表达。BRCA基因是与DNA损伤有关的肿瘤抑制基因。由于DNA修复机制存在缺陷,BRCA基因的修复和突变可能会增加患乳腺癌和/或卵巢癌的风险。但是,BRCA状态与TNBC之间的关系需要进一步研究和验证。这项荟萃分析的目的是评估BRCA状态与TNBC之间的关联。我们系统地搜索了MEDLINE(PubMed),Embase和Cochrane图书馆的电子数据库,以确定1959年4月至2017年11月的相关出版物。研究的数据通过使用STATA软件的荟萃分析进行了检验,以计算优势比。 (OR),采用固定效应和随机效应模型的置信区间(CI)为95%。我们从527个出版物中筛选了16项合格的研究,涉及46,870名乳腺癌患者,包括868个BRCA1突变(BRCA1 Mut )携带者,739个BRCA2突变(BRCA2 Mut )携带者和45,263个非运营商。结果表明,与BRCA2 Mut 携带者相比,携带BRCA1 Mut 携带者的乳腺癌患者更可能患有TNBC(OR:3.292; 95%CI:2.773–3.909)或非运营商(或:8.889; 95%CI:6.925-11.410)。此外,携带BRCA1 Mut 携带者的乳腺癌患者比 BRCA2 <的携带者的核级高表达和大肿瘤负荷(> 2 cm)明显更为常见。 em> Mut 载波(OR:2.663; 95%CI:1.731–4.097; P = 0.211)或非载波(OR:1.577; 95%CI:1.067 –2.331; P = 0.157)。数据表明患有 BRCA1 Mut 的乳腺癌患者更可能患有TNBC,高核级和更大的肿瘤负担。

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