Oncology Unit, 2nd Department of Internal Medicine, Attikon University Hospital, National Kapodistrian University of Athens, Greece.
Oncology Unit, 2nd Department of Internal Medicine, Attikon University Hospital, National Kapodistrian University of Athens, Greece.
Cancer Treat Rev. 2015 Jan;41(1):1-8. doi: 10.1016/j.ctrv.2014.10.008. Epub 2014 Nov 6.
Approximately 5-10% of breast cancer cases might be inheritable, up to 30% of which are due to BRCA1/2 mutations. During the past few years and thanks to technology evolution, we have been witnesses of an intensive search of additional genes with similar characteristics, under the premise that successful gene discovery will provide substantial opportunities for primary and secondary prevention of breast cancer. Consequently, new genes have emerged as breast cancer susceptibility genes, including rare germline mutations in high penetrant genes, such as TP53 and PTEN, and more frequent mutations in moderate penetrant genes, such as CHEK2, ATM and PALB2. This review will summarize current data on new findings in breast cancer susceptibility genes.
约 5-10%的乳腺癌病例可能是遗传性的,其中多达 30%归因于 BRCA1/2 突变。在过去几年中,得益于技术的发展,我们见证了对具有类似特征的其他基因的密集搜索,前提是成功发现基因将为乳腺癌的一级和二级预防提供实质性机会。因此,新的基因已经成为乳腺癌易感性基因,包括高外显率基因中的罕见种系突变,如 TP53 和 PTEN,以及中外显率基因中更常见的突变,如 CHEK2、ATM 和 PALB2。本文将总结乳腺癌易感性基因新发现的当前数据。