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Familial Renal Cancer: Molecular Genetics and Surgical Management
Author(s) -
Glen W. Barrisford,
Eric A. Singer,
Inger L. Rosner,
W. Marston Linehan,
Gennady Bratslavsky
Publication year - 2011
Publication title -
international journal of surgical oncology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.432
H-Index - 22
eISSN - 2090-1410
pISSN - 2090-1402
DOI - 10.1155/2011/658767
Subject(s) - renal cell carcinoma , kidney cancer , medicine , cancer , disease , bioinformatics , molecular genetics , birt–hogg–dubé syndrome , von hippel–lindau disease , kidney , genetic counseling , pathology , genetics , cancer research , oncology , biology , gene , surgery , pneumothorax
Familial renal cancer (FRC) is a heterogeneous disorder comprised of a variety of subtypes. Each subtype is known to have unique histologic features, genetic alterations, and response to therapy. Through the study of families affected by hereditary forms of kidney cancer, insights into the genetic basis of this disease have been identified. This has resulted in the elucidation of a number of kidney cancer gene pathways. Study of these pathways has led to the development of novel targeted molecular treatments for patients affected by systemic disease. As a result, the treatments for families affected by von Hippel-Lindau (VHL), hereditary papillary renal carcinoma (HPRC), hereditary leiomyomatosis renal cell carcinoma (HLRCC), and Birt-Hogg-Dubé (BHD) are rapidly changing. We review the genetics and contemporary surgical management of familial forms of kidney cancer.

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