Nagy Rebecca, Sweet Kevin, Eng Charis
Clinical Cancer Genetics Program, Comprehensive Cancer Center, Division of Human Genetics, Department of Internal Medicine, The Ohio State University, Columbus 43221, USA.
Oncogene. 2004 Aug 23;23(38):6445-70. doi: 10.1038/sj.onc.1207714.
The past two decades have brought many important advances in our understanding of the hereditary susceptibility to cancer. Approximately 5-10% of all cancers are inherited, the majority in an autosomal dominant manner with incomplete penetrance. While this is a small fraction of the overall cancer burden worldwide, the molecular genetic discoveries that have resulted from the study of families with heritable cancer have not only changed the way these families are counselled and managed, but have shed light on molecular regulatory pathways important in sporadic tumour development as well. In this review, we consider 10 of the more highly penetrant cancer syndromes, with emphasis on those predisposing to breast, colon, and/or endocrine neoplasia. We discuss the prevalence, penetrance, and tumour spectrum associated with these syndromes, as well as their underlying genetic defects.
在过去二十年里,我们对癌症遗传易感性的理解取得了许多重要进展。所有癌症中约5%-10%是遗传性的,大多数以常染色体显性方式遗传,且具有不完全外显率。虽然这在全球总体癌症负担中占比很小,但对遗传性癌症家族的研究所带来的分子遗传学发现,不仅改变了为这些家族提供咨询和管理的方式,还揭示了散发性肿瘤发生过程中重要的分子调控途径。在这篇综述中,我们考虑了10种外显率较高的癌症综合征,重点关注那些易患乳腺癌、结肠癌和/或内分泌肿瘤的综合征。我们讨论了与这些综合征相关的患病率、外显率和肿瘤谱,以及它们潜在的基因缺陷。