Genetic factors involved in breast cancer

R. Ursu, Radu Alexandru Truica, Alexandra Cojocaru, Diana Prepelita, L. Pop, V. Rădoi, N. Bacalbaşa, I. Bălescu
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Abstract

According to the World Health Organization, as of 2021, breast cancer is the most common malignancy in women worldwide, accounting for up to 12% of all new cancer cases diagnosed each year. Moreover, breast cancer is the second leading cause of cancer-related death in women. In Romania, over 7.000 new breast cancer cases are diagnosed every year, with 80% of them being diagnosed in an advanced stage where treatment does not lead to curing the disease but only to prolonging life. The genetic factors identified to be involved in breast cancer risk comprise numerous biomarkers including the highly penetrant breast cancer susceptibility genes (BRCA1, BRCA2, PTEN, TP53, CDH1 and STK11), a number of genes with more moderate penetrance (CHEK2, BRIP1, ATM, PALB2) and low penetrance alleles. Prediction models suggest that, for now, there is a low probability to discover new high-penetrance genes.
遗传因素与乳腺癌有关
根据世界卫生组织的数据,截至2021年,乳腺癌是全球女性中最常见的恶性肿瘤,占每年新诊断癌症病例的12%。此外,乳腺癌是妇女癌症相关死亡的第二大原因。在罗马尼亚,每年诊断出7 000多例新的乳腺癌病例,其中80%被诊断为晚期,治疗不能治愈疾病,只能延长生命。已确定的与乳腺癌风险相关的遗传因素包括许多生物标志物,包括高渗透的乳腺癌易感基因(BRCA1、BRCA2、PTEN、TP53、CDH1和STK11)、一些外显率较中等的基因(CHEK2、BRIP1、ATM、PALB2)和低外显率的等位基因。预测模型显示,目前发现新的高外显率基因的可能性很低。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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