Literature DB >> 7500607

[Osteosarcoma in 2 siblings. A case report].

F Danckwerth1, P Wuisman, J Ritter, S Blasius, H Jürgens, T Ozaki, W Winkelmann.   

Abstract

With a brother and sister, osteosarcoma developed at the age of 11 and 14 respectively. With both there was no previous retinoblastoma or other bone disease with a proclivity to develop osteosarcoma. We discuss possible explanations for familial aggregation of osteosarcoma, citing external or genetic factors. We suggest that it is the retinoblastoma gene RB and the tumor suppressor gene p53 which play an important part in the development of osteosarcoma.

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Year:  1995        PMID: 7500607     DOI: 10.1055/s-2008-1046555

Source DB:  PubMed          Journal:  Klin Padiatr        ISSN: 0300-8630            Impact factor:   1.349


  2 in total

1.  Cytoplasmic and/or nuclear accumulation of the beta-catenin protein is a frequent event in human osteosarcoma.

Authors:  Rex C Haydon; Andrea Deyrup; Akira Ishikawa; Robert Heck; Wei Jiang; Lan Zhou; Tao Feng; David King; Hongwei Cheng; Benjamin Breyer; Terrance Peabody; Michael A Simon; Anthony G Montag; Tong-Chuan He
Journal:  Int J Cancer       Date:  2002-12-01       Impact factor: 7.396

2.  A Rb1 promoter variant with reduced activity contributes to osteosarcoma susceptibility in irradiated mice.

Authors:  Michael Rosemann; Iria Gonzalez-Vasconcellos; Tanja Domke; Virginija Kuosaite; Ralf Schneider; Markus Kremer; Jack Favor; Michaela Nathrath; Michael J Atkinson
Journal:  Mol Cancer       Date:  2014-08-04       Impact factor: 27.401

  2 in total

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