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遗传性乳腺癌和卵巢癌的种系基因检测:风险评估的当前概念。

Germline Genetic Testing for Hereditary Breast and Ovarian Cancer: Current Concepts in Risk Evaluation.

机构信息

Department of Oncology, Mayo Clinic, Rochester, Minnesota 55905, USA

Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota 55901, USA

出版信息

Cold Spring Harb Perspect Med. 2024 Aug 1;14(8):a041318. doi: 10.1101/cshperspect.a041318.

Abstract

Our understanding of hereditary breast and ovarian cancer has significantly improved over the past two decades. In addition to , pathogenic variants in several other DNA-repair genes have been shown to increase the risks of breast and ovarian cancer. The magnitude of cancer risk is impacted not only by the gene involved, but also by family history of cancer, polygenic risk scores, and, in certain genes, pathogenic variant type or location. While estimates of breast and ovarian cancer risk associated with pathogenic variants are available, these are predominantly based on studies of high-risk populations with young age at diagnosis of cancer, multiple primary cancers, or family history of cancer. More recently, breast cancer risk for germline pathogenic variant carriers has been estimated from population-based studies. Here, we provide a review of the field of germline genetic testing and risk evaluation for hereditary breast and ovarian cancers in high-risk and population-based settings.

摘要

在过去的二十年中,我们对遗传性乳腺癌和卵巢癌的认识有了显著提高。除了 BRCA1 和 BRCA2 基因外,其他几个 DNA 修复基因的致病性变异也被证明会增加乳腺癌和卵巢癌的风险。癌症风险的大小不仅受涉及的基因影响,还受癌症家族史、多基因风险评分以及某些基因中致病性变异类型或位置的影响。虽然与致病性变异相关的乳腺癌和卵巢癌风险估计已经存在,但这些主要基于癌症诊断年龄较轻、有多个原发性癌症或癌症家族史的高危人群的研究。最近,已经从基于人群的研究中估计了种系致病性变异携带者的乳腺癌风险。在这里,我们综述了高危人群和基于人群的遗传检测和遗传性乳腺癌和卵巢癌风险评估领域。

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