Mutation and expression analysis of the p73 gene in prostate cancer

Akira Yokomizo, Ming Mai, David G. Bostwick, Donald J. Tindall, Junqi Qian, Liang Cheng, Robert B. Jenkins, David I. Smith, Wanguo Liu

Research output: Contribution to journalArticle

35 Scopus citations

Abstract

BACKGROUND. p53 is the most highly mutated tumor suppressor gene in human cancers. Recently, p73, a first homologue of p53, was identified and considered to be an imprinted tumor suppressor gene. Thus, we analyzed the possible role of p73 in human prostate cancers. METHODS. We investigated the expression levels and expressed allelotypes and searched for mutations in the p73 gene in 27 primary prostate cancers with matched normal tissues as well as in four prostate cell lines. RESULTS. Allelic expression analysis using polymorphisms in exons 2 and 5 revealed that p73 is biallelically expressed in both normal and tumor tissues, suggesting that p73 is not imprinted in prostate tissues. Quantitative PCR demonstrated that p73 expression is the same in both normal and tumor prostate tissues. Denaturing high-performance liquid chromatography and DNA sequencing revealed that there were no tumor- specific mutations in the p73 gene at the genomic level. CONCLUSIONS. These data indicate that alterations of p73, including mutations, changes in message abundance, and changes in allelic expression, are likely to be rare in early-stage prostate cancer, and that p73 could be a tissue-specific imprinting gene.

Original languageEnglish (US)
Pages (from-to)94-100
Number of pages7
JournalProstate
Volume39
Issue number2
DOIs
StatePublished - Apr 1 1999
Externally publishedYes

    Fingerprint

Keywords

  • Allelic expression
  • Imprinting
  • Mutation
  • P73
  • Prostate cancer

ASJC Scopus subject areas

  • Oncology
  • Urology

Cite this

Yokomizo, A., Mai, M., Bostwick, D. G., Tindall, D. J., Qian, J., Cheng, L., Jenkins, R. B., Smith, D. I., & Liu, W. (1999). Mutation and expression analysis of the p73 gene in prostate cancer. Prostate, 39(2), 94-100. https://doi.org/10.1002/(SICI)1097-0045(19990501)39:2<94::AID-PROS3>3.0.CO;2-W