MDM2 SNP309 G allele decreases risk but does not affect onset age or survival of Chinese leukaemia patients

Eur J Cancer. 2008 Mar;44(5):760-6. doi: 10.1016/j.ejca.2008.02.007. Epub 2008 Mar 7.

Abstract

Although mutations in p53 are rare in leukaemia, MDM2, the negative regulator of p53, is often overexpressed. Recently, a single nucleotide polymorphism (SNP) in the MDM2 promoter--within the oestrogen-receptor-binding region--resulting in either a G or T allele was shown to affect its transcription, with elevated MDM2 being produced when it is a G allele. Expectedly, SNP309G females were found to be at a higher risk of accelerated onset of cancers. We have therefore analysed, in a pilot study, whether the status of MDM2 SNP309 and p53 codon-72 polymorphism, which was also shown to affect cancer predisposition, would affect cancer risk, onset age, overall survival and response to therapy in Chinese leukaemia patients. p53 SNP was not associated with any of the parameters. However, in contrast to expectations, the MDM2 SNP309G allele was associated with reduced risk of leukaemia. No other association was found between SNP309 and other parameters in both males and females. Thus, the data highlights ethnic differences in the effects of this SNP on cancer risk.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Age of Onset
  • Antineoplastic Agents / therapeutic use
  • China / epidemiology
  • Female
  • Genes, p53 / genetics*
  • Genotype
  • Humans
  • Leukemia / drug therapy
  • Leukemia / genetics*
  • Leukemia / mortality
  • Male
  • Middle Aged
  • Mutation / genetics*
  • Pilot Projects
  • Polymorphism, Single Nucleotide / genetics*
  • Proto-Oncogene Proteins c-mdm2 / genetics*
  • Risk Factors
  • Survival Analysis

Substances

  • Antineoplastic Agents
  • MDM2 protein, human
  • Proto-Oncogene Proteins c-mdm2