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家族性肾细胞癌的遗传学。

Genetics of familial renal cancers.

机构信息

University of Birmingham Centre for Rare Diseases and Personalised Medicine and Medical and Molecular Genetics, School of Clinical and Experimental Medicine, College of Medical and Dental Sciences, Institute of Biomedical Research, University of Birmingham, Edgbaston, Birmingham, UK.

出版信息

Nephron Exp Nephrol. 2011;118(1):e21-6. doi: 10.1159/000320892. Epub 2010 Nov 11.

Abstract

Renal cell carcinoma (RCC) is a heterogeneous disorder. A variety of histopathological subtypes occur, and the molecular mechanisms associated with these subtypes can differ. Only a small fraction of all RCC is accounted for by inherited cases (e.g. von Hippel-Lindau disease, Birt-Hogg-Dubé syndrome, hereditary leiomyomatosis renal cell cancer), but such cases can pose specific clinical management issues and offer opportunities for early cancer detection and prevention. Furthermore, inherited RCC syndromes have provided important paradigms to study the molecular basis of renal tumourigenesis. The identification of molecular mechanisms of carcinogenesis in inherited RCC syndromes should lead to novel approaches to personalized therapeutics.

摘要

肾细胞癌(RCC)是一种异质性疾病。存在多种组织病理学亚型,与这些亚型相关的分子机制可能不同。遗传性病例(如 von Hippel-Lindau 病、Birt-Hogg-Dubé 综合征、遗传性平滑肌瘤病肾细胞癌)仅占所有 RCC 的一小部分,但此类病例可能会带来特定的临床管理问题,并提供早期癌症检测和预防的机会。此外,遗传性 RCC 综合征为研究肾癌发生的分子基础提供了重要范例。鉴定遗传性 RCC 综合征中的致癌分子机制应导致针对个体化治疗的新方法。

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