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Prevalence of BRCA1 and BRCA2 gene mutations in Chinese patients with high‐risk breast cancer

机译:高危乳腺癌患者BRCA1和BRCA2基因突变的患病率

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Background Breast cancer is the most common cancer among women worldwide. Here, we report the prevalence of BRCA1/2 mutations in patients with high‐risk breast cancer from Inner Mongolia and Jilin, China, which was a part of a nationwide project on the detection of BRCA1/2 mutations in Chinese patients with hereditary breast cancer. Methods According to the criteria, index patients from a total of 245 independent families were initially recruited. All 49 exons of BRCA1 and BRCA2 and adjacent noncoding regions were screened for mutations based on next‐generation sequencing from collected saliva. Results We detected 17 BRCA1/2 variants in 18 of 216 (8.3%) index patients with high‐risk breast cancer. Among these, seven mutations were novel, including four BRCA1 mutations (c.123_124delCAinsAT, c.5093_5096delCTAA, c.5396‐2AG, and c.2054delinsGAAGAGTAACAAGTAAGAAGAGTAACAAGAAG), and three BRCA2 mutations (c.304AT, c.7552_7553insT, and c.9548_9549insA). The BRCA1/2 variants were identified in 14% (8/57) of the patients with triple‐negative breast cancer and in 6.3% (10/159) of the patients with non‐triple‐negative breast cancer. There was no significant difference between the two groups ( p ?=?0.07). A higher frequency for BRCA1 mutations was observed in patients with triple‐negative breast cancer than in those with non‐triple‐negative breast cancer (12.3% vs. 2.5%, p ?=?0.004). The frequencies of the BRCA2 mutations were not significantly different between patients with triple‐negative breast cancer and those with non‐triple‐negative breast cancer (1.8% vs. 3.8%, p ?=?0.46). Conclusion We found that patients with triple‐negative breast cancer had a higher frequency of BRCA1 mutations than those with non‐triple‐negative breast cancer. In this study, no significant associations between the BRCA1/2 mutation status and age, family history of breast cancer, ovarian cancer, pancreatic cancer and prostate cancer, number of primary lesions, tumor size, or lymph node metastasis were observed.
机译:背景技术乳腺癌是全世界妇女中最常见的癌症。在这里,我们报告了来自中国内蒙古和吉林的高危乳腺癌患者BRCA1 / 2突变的患病率,这是全国范围的遗传乳腺癌患者BRCA1 / 2突变的全国性项目的一部分。 。方法根据标准,最初招募了总共245个独立家庭的指标患者。基于来自收集的唾液的下一代测序,筛选所有49个BRCA1和BRCA2和相邻的非分量区域。结果我们在216例(8.3%)指数患者中检测到17例BRCA1 / 2变体,高危乳腺癌。其中,七种突变是新的,包括四种BRCA1突变(C.123_124Delcainsat,C.5093_5096delctaA,C.5396-2A> G,C.2054DelinsgaagagtaacaagtaagaagagaacaAg)和三种BRCA2突变(C.304A> T,C.7552_7553,和c.9548_9549 insa)。 BRCA1 / 2变体在14%(8/57)患者中鉴定了三阴性乳腺癌的患者,6.3%(10/159)的非三阴性乳腺癌患者。两组之间没有显着差异(p?= 0.07)。在三阴性乳腺癌患者中观察到BRCA1突变的较高频率,而不是非三阴性乳腺癌的患者(12.3%vs.2.5%,p?= 0.004)。三阴性乳腺癌患者和具有非三阴性乳腺癌的患者之间的BRCA2突变的频率没有显着差异(1.8%,P?= 0.46)。结论我们发现,三重阴性乳腺癌的患者具有比具有非三重阴性乳腺癌的突变的频率较高。在这项研究中,BRCA1 / 2突变状态和年龄之间没有重大关联,乳腺癌,卵巢癌,胰腺癌和前列腺癌,初级病变数,肿瘤大小或淋巴结转移的数量。

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