Familial adult renal neoplasia


Autoria(s): Takahashi, M.; Kahnoski, R.; Gross, D.; Nicol, D.; Teh, B. T.
Contribuinte(s)

Eamonn R. Maher

Data(s)

01/01/2002

Resumo

Our understanding of the molecular mechanisms underlying the tumorigenesis of renal cell carcinoma (RCC) has partially come from studies of RCC related familial cancer syndromes such as von Hippel-Lindau (VHL) disease and hereditary papillary RCC (HPRC). These studies have led to the identification of RCC related genes, which, besides allowing accurate diagnosis of these diseases, have been found mutated or abnormally expressed in the sporadic counterparts of these familial renal tumours. To date, a number of renal tumour related syndromes have been described. We review recent advances in this field and discuss a genetic approach to managing familial cases of renal tumours occasionally encountered by cancer geneticists and urologists.

Identificador

http://espace.library.uq.edu.au/view/UQ:63411

Idioma(s)

eng

Publicador

BMJ Publishing Group

Palavras-Chave #Genetics & Heredity #Tumor-suppressor Gene #Hogg-dube Syndrome #Hippel-lindau Protein #Cell-carcinoma #Tuberous Sclerosis #Met Protooncogene #Kidney-disease #Vhl #Multiple #Cancer #hereditary #kidney tumours #syndromes #C1 #730109 Surgical methods and procedures #110323 Surgery
Tipo

Journal Article