Literature DB >> 23595191

Heritable retinoblastoma and accelerated aortic valve disease.

L R Abeyratne1, J E Kingston, Z Onadim, S W Dubrey.   

Abstract

Heritable retinoblastoma is associated with a germline mutation in the tumour suppressor gene RBI. The Rb protein (pRb) arises from the RB1 gene, which was the first demonstrated cancer susceptibility gene in humans. Second primary malignancies are recognised complications of retinoblastoma. Furthermore, pRb is implicated in valve remodelling in calcific aortic valve disease. We report a family with hereditary retinoblastoma and associated secondary primary malignancies. There are two interesting aspects to this family. The first is the concept of 'cancer susceptibility genes'; the RBI gene being the first reported in humans. A further feature of note is that two family members also have bicuspid aortic valves. We discuss a potential association between the gene defect responsible for retinoblastoma (with its associated propensity for further malignancies) and accelerated deterioration of the bicuspid aortic valve in the proband carrying this gene defect.

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Year:  2013        PMID: 23595191      PMCID: PMC3645137          DOI: 10.1136/bcr-2013-009233

Source DB:  PubMed          Journal:  BMJ Case Rep        ISSN: 1757-790X


  4 in total

1.  Clinical and pathophysiological implications of a bicuspid aortic valve.

Authors:  Paul W M Fedak; Subodh Verma; Tirone E David; Richard L Leask; Richard D Weisel; Jagdish Butany
Journal:  Circulation       Date:  2002-08-20       Impact factor: 29.690

2.  Notch-dependent cell cycle arrest is associated with downregulation of minichromosome maintenance proteins.

Authors:  Michela Noseda; Kyle Niessen; Graeme McLean; Linda Chang; Aly Karsan
Journal:  Circ Res       Date:  2005-06-23       Impact factor: 17.367

3.  Cancer incidence after retinoblastoma. Radiation dose and sarcoma risk.

Authors:  F L Wong; J D Boice; D H Abramson; R E Tarone; R A Kleinerman; M Stovall; M B Goldman; J M Seddon; N Tarbell; J F Fraumeni; F P Li
Journal:  JAMA       Date:  1997-10-15       Impact factor: 56.272

4.  Frequent constitutional C to T mutations in CGA-arginine codons in the RB1 gene produce premature stop codons in patients with bilateral (hereditary) retinoblastoma.

Authors:  J K Cowell; T Smith; B Bia
Journal:  Eur J Hum Genet       Date:  1994       Impact factor: 4.246

  4 in total
  1 in total

1.  Conditional deletion of RB1 in the Tie2 lineage leads to aortic valve regurgitation.

Authors:  Marina Freytsis; Lauren Baugh; Zhiyi Liu; Irene Georgakoudi; Philip W Hinds; Lauren D Black; Gordon S Huggins
Journal:  PLoS One       Date:  2018-01-05       Impact factor: 3.240

  1 in total

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