Literature DB >> 21071978

Genetics of familial renal cancers.

Eamonn R Maher1.   

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.
Copyright © 2010 S. Karger AG, Basel.

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Year:  2010        PMID: 21071978     DOI: 10.1159/000320892

Source DB:  PubMed          Journal:  Nephron Exp Nephrol        ISSN: 1660-2129


  10 in total

1.  The tumor susceptibility gene TMEM127 is mutated in renal cell carcinomas and modulates endolysosomal function.

Authors:  Y Qin; Y Deng; C J Ricketts; S Srikantan; E Wang; E R Maher; P L M Dahia
Journal:  Hum Mol Genet       Date:  2013-12-13       Impact factor: 6.150

2.  Familial renal cancer as an indicator of hereditary leiomyomatosis and renal cell cancer syndrome.

Authors:  Victoria M Raymond; Casey M Herron; Thomas J Giordano; Stephen B Gruber
Journal:  Fam Cancer       Date:  2012-03       Impact factor: 2.375

Review 3.  Hereditary Renal Tumor Syndromes: Update on Diagnosis and Management.

Authors:  Sonia Gaur; Baris Turkbey; Peter Choyke
Journal:  Semin Ultrasound CT MR       Date:  2016-10-14       Impact factor: 1.875

4.  Prevalence, birth incidence, and penetrance of von Hippel-Lindau disease (vHL) in Denmark.

Authors:  Marie Louise Mølgaard Binderup; Michael Galanakis; Esben Budtz-Jørgensen; Michael Kosteljanetz; Marie Luise Bisgaard
Journal:  Eur J Hum Genet       Date:  2016-12-14       Impact factor: 4.246

5.  DNA methylation profiling distinguishes histological subtypes of renal cell carcinoma.

Authors:  Amy A Slater; Majed Alokail; Dean Gentle; Masahiro Yao; Gyula Kovacs; Eamonn R Maher; Farida Latif
Journal:  Epigenetics       Date:  2013-02-21       Impact factor: 4.528

6.  Molecular and phenotypic evaluation of a novel germline TMEM127 mutation with an uncommon clinical presentation.

Authors:  Yilun Deng; Shahida K Flores; ZiMing Cheng; Yuejuan Qin; Robin C Schwartz; Carl Malchoff; Patricia L M Dahia
Journal:  Endocr Relat Cancer       Date:  2017-08-30       Impact factor: 5.678

7.  Hereditary leiomyomatosis and renal cell cancer presenting as metastatic kidney cancer at 18 years of age: implications for surveillance.

Authors:  Karin Y van Spaendonck-Zwarts; Sadhanna Badeloe; Sjoukje F Oosting; Sjoerd Hovenga; Harry J F Semmelink; R Jeroen A van Moorselaar; Jan Hein van Waesberghe; Arjen R Mensenkamp; Fred H Menko
Journal:  Fam Cancer       Date:  2012-03       Impact factor: 2.375

8.  UBE2QL1 is disrupted by a constitutional translocation associated with renal tumor predisposition and is a novel candidate renal tumor suppressor gene.

Authors:  Naomi C Wake; Christopher J Ricketts; Mark R Morris; Elena Prigmore; Susan M Gribble; Anne-Bine Skytte; Michael Brown; Noel Clarke; Rosamonde E Banks; Shirley Hodgson; Andrew S Turnell; Eamonn R Maher; Emma R Woodward
Journal:  Hum Mutat       Date:  2013-10-07       Impact factor: 4.878

9.  Renal cell tumour characteristics in patients with the Birt-Hogg-Dubé cancer susceptibility syndrome: a retrospective, multicentre study.

Authors:  Patrick R Benusiglio; Sophie Giraud; Sophie Deveaux; Arnaud Méjean; Jean-Michel Correas; Dominique Joly; Marc-Olivier Timsit; Sophie Ferlicot; Virginie Verkarre; Caroline Abadie; Dominique Chauveau; Dominique Leroux; Marie-Françoise Avril; Jean-François Cordier; Stéphane Richard
Journal:  Orphanet J Rare Dis       Date:  2014-10-29       Impact factor: 4.123

Review 10.  Clinical and Molecular Features of Renal and Pheochromocytoma/Paraganglioma Tumor Association Syndrome (RAPTAS): Case Series and Literature Review.

Authors:  Ruth T Casey; Anne Y Warren; Jose Ezequiel Martin; Benjamin G Challis; Eleanor Rattenberry; James Whitworth; Katrina A Andrews; Thomas Roberts; Graeme R Clark; Hannah West; Philip S Smith; France M Docquier; Fay Rodger; Vicki Murray; Helen L Simpson; Yvonne Wallis; Olivier Giger; Maxine Tran; Susan Tomkins; Grant D Stewart; Soo-Mi Park; Emma R Woodward; Eamonn R Maher
Journal:  J Clin Endocrinol Metab       Date:  2017-11-01       Impact factor: 5.958

  10 in total

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