P57 (KIP2) polymorphisms and breast cancer risk

Hum Genet. 1999 Jan;104(1):83-8. doi: 10.1007/s004390050914.

Abstract

A previous report in this journal has suggested that germline deletions in the proline-alanine-rich (PAPA-repeat) region of P57 (KIP2) are associated with increased risk of a variety of cancers, including breast cancer. We have analyzed the association of P57 PAPA-repeat deletion polymorphisms and breast cancer risk as part of a population-based case-control study of breast cancer. We have not observed an association between the presence of one or two copies of deletion polymorphisms in P57 and breast cancer risk (adjusted odds ratio: 1.1, 95% confidence interval: 0.6-2.0). Further investigation is necessary to determine the functional significance of P57 deletion polymorphisms and their potential relationship with disease.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Breast Neoplasms / epidemiology
  • Breast Neoplasms / genetics*
  • Case-Control Studies
  • Cyclin-Dependent Kinase Inhibitor p57
  • Female
  • Humans
  • Middle Aged
  • North Carolina / epidemiology
  • Nuclear Proteins / chemistry
  • Nuclear Proteins / genetics*
  • Odds Ratio
  • Polymorphism, Genetic / genetics*
  • Repetitive Sequences, Nucleic Acid
  • Risk Factors
  • Sequence Deletion

Substances

  • CDKN1C protein, human
  • Cyclin-Dependent Kinase Inhibitor p57
  • Nuclear Proteins