The presence of p53 mutations in human osteosarcomas correlates with high levels of genomic instability Journal Article


Authors: Overholtzer, M.; Rao, P. H.; Favis, R.; Lu, X. Y.; Elowitz, M. B.; Barany, F.; Ladanyi, M.; Gorlick, R.; Levine, A. J.
Article Title: The presence of p53 mutations in human osteosarcomas correlates with high levels of genomic instability
Abstract: The p53 gene is a critical tumor suppressor that is inactivated in a majority of cancers. The central role of p53 in response to stresses such as DNA damage, hypoxia, and oncogene activation underlies this high frequency of negative selection during tumorigenic transformation. Mutations in p53 disrupt checkpoint responses to DNA damage and result in the potential for destabilization of the genome. Consistent with this, p53 mutant cells have been shown to accumulate genomic alterations in cell culture, mouse models, and some human tumors. The relationship between p53 mutation and genomic instability in human osteosarcoma is addressed in this report. Similar to some other primary human tumors, the mutation of p53 correlates significantly with the presence of high levels of genomic instability in osteosarcomas. Surprisingly, osteosarcomas harboring an amplification of the HDM2 oncogene, which inhibits the tumor-suppressive properties of p53, do not display high levels of genomic instability. These results demonstrate that the inactivation of p53 in osteosarcomas directly by mutation versus indirectly by HDM2 amplification may have different cellular consequences with respect to the stability of the genome.
Keywords: osteosarcoma; human tissue; gene mutation; mutation; proto-oncogene proteins; polymerase chain reaction; dna damage; gene amplification; cancer model; carcinogenesis; nuclear proteins; cancer inhibition; gene number; oncogene; tumor suppressor gene; cell culture; dna, neoplasm; genetic stability; genome; nucleic acid hybridization; proto-oncogene proteins c-mdm2; genes, p53; humans; human; priority journal; article; oncogene hdm2
Journal Title: Proceedings of the National Academy of Sciences of the United States of America
Volume: 100
Issue: 20
ISSN: 0027-8424
Publisher: National Academy of Sciences  
Date Published: 2003-09-30
Start Page: 11547
End Page: 11552
Language: English
DOI: 10.1073/pnas.1934852100
PUBMED: 12972634
PROVIDER: scopus
PMCID: PMC208795
DOI/URL:
Notes: Export Date: 12 September 2014 -- Source: Scopus
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  1. Richard G Gorlick
    121 Gorlick
  2. Marc Ladanyi
    1326 Ladanyi