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男性乳腺癌的基因图谱

Genetic Landscape of Male Breast Cancer.

作者信息

Campos Fernando Augusto Batista, Rouleau Etienne, Torrezan Giovana Tardin, Carraro Dirce Maria, Casali da Rocha José Claudio, Mantovani Higor Kassouf, da Silva Leonardo Roberto, Osório Cynthia Aparecida Bueno de Toledo, Moraes Sanches Solange, Caputo Sandrine M, Santana Dos Santos Elizabeth

机构信息

Deparment of Medical Oncology, A.C.Camargo Cancer Center, Sao Paulo 01509-010, Brazil.

Department of Medical Biology and Pathology, Gustave Roussy, Cancer Genetics Laboratory, Gustave Roussy, 94805 Villejuif, France.

出版信息

Cancers (Basel). 2021 Jul 15;13(14):3535. doi: 10.3390/cancers13143535.

Abstract

Male breast cancer (MBC) is now considered molecularly different from female breast cancer (FBC). Evidence from studies indicates that common genetic and epigenetic features of FBC are not shared with those diagnosed in men. Genetic predisposition is likely to play a significant role in the tumorigenesis of this rare disease. Inherited germline variants in and account for around 2% and 10% of MBC cases, respectively, and the lifetime risk of breast cancer for men harboring and mutations is 1.2% and 6.8%. As for FBC, pathogenic mutations in other breast cancer genes have also been recently associated with an increased risk of MBC, such as and mutations. However, while multigene germline panels have been extensively performed for BC female patients, the rarity of MBC has resulted in limited data to allow the understanding of the magnitude of risk and the contribution of recently identified moderate penetrance genes of FBC for MBC predisposition. This review gathers available data about the germline genetic landscape of men affected by breast cancer, estimated risk associated with these genetic variants, and current guidelines for clinical management.

摘要

男性乳腺癌(MBC)目前被认为在分子层面上与女性乳腺癌(FBC)有所不同。研究证据表明,FBC常见的基因和表观遗传特征在男性乳腺癌患者中并不存在。遗传易感性可能在这种罕见疾病的肿瘤发生过程中发挥重要作用。在男性乳腺癌病例中,BRCA1和BRCA2的遗传性种系变异分别约占2%和10%,携带BRCA1和BRCA2突变的男性患乳腺癌的终生风险分别为1.2%和6.8%。与FBC一样,其他乳腺癌基因的致病性突变最近也与MBC风险增加有关,如PALB2和ATM突变。然而,虽然已对FBC女性患者广泛开展了多基因种系检测,但MBC的罕见性导致数据有限,难以了解风险程度以及最近发现的FBC中度外显率基因对MBC易感性的影响。本综述收集了有关患乳腺癌男性的种系遗传情况、与这些遗传变异相关的估计风险以及当前临床管理指南的现有数据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/06b3/8305894/9c665c97b87b/cancers-13-03535-g001.jpg

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