Tissue-specific apoptotic effects of the p53 codon 72 polymorphism in a mouse model

Gregory A. Azzam, Amanda K. Frank, Monica Hollstein, Maureen E. Murphy

Research output: Contribution to journalReview articlepeer-review

26 Scopus citations

Abstract

Currently there are several dozen human polymorphisms that have been loosely associated with cancer risk. Correlating such variants with cancer risk has been challenging, primarily due to factors such as genetic heterogeneity, contributions of diet and environmental factors, and the difficulty in obtaining large sample sizes for analysis. Such difficulties can be circumvented with the establishment of mouse models for human variants. Recently, several groups have modeled human cancer susceptibility polymorphisms in the mouse. Remarkably, in each case these mouse models have accurately reflected human phenotypes, and clarified the contribution of these variants to cancer risk. We recently reported on a mouse model for the codon 72 polymorphism in p53, and found that this polymorphism regulates the ability to cooperate with NFκB and induce apoptosis. Here-in we present evidence that this polymorphism impacts the apoptotic function of p53 in a tissue-specific manner; such tissue-specific effects of polymorphic variants represent an added challenge to human cancer risk association studies. The data presented here support the premise that modeling human polymorphisms in the mouse represents a powerful tool to assess the impact of these variants on cancer risk, progression and therapy.

Original languageEnglish (US)
Pages (from-to)1352-1355
Number of pages4
JournalCell Cycle
Volume10
Issue number9
DOIs
StatePublished - May 1 2011
Externally publishedYes

Keywords

  • Apoptosis
  • B
  • Codon 72
  • NFκ
  • p53
  • Polymorphism

ASJC Scopus subject areas

  • Molecular Biology
  • Developmental Biology
  • Cell Biology

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