Retinoblastoma gene mutations in primary human prostate cancer

Prostate. 1995 Dec;27(6):314-20. doi: 10.1002/pros.2990270604.

Abstract

Structural alterations in the entire coding regions (exons 1 to 27) of the retinoblastoma (RB) gene in primary human prostate cancers were investigated, using polymerase chain reaction and single strand conformational polymorphism analysis of RNA. Of 25 samples obtained from patients, four (16.4%) were found to have RB alterations. DNA sequencing of the PCR products revealed point mutations resulting in single amino-acid substitutions of exons 6 and 19 in two cases, and base deletions of exons 8 and 17 in two cases. Two of four cases with RB mutations were moderately differentiated localized tumors and other two with RB mutations were poorly differentiated tumors with metastases. Our results suggest that RB gene mutation is involved in progression steps of prostate carcinogenesis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenocarcinoma / chemistry
  • Adenocarcinoma / genetics*
  • Adenocarcinoma / pathology
  • Base Sequence
  • DNA Primers / chemistry
  • DNA, Neoplasm / analysis
  • DNA, Neoplasm / chemistry
  • DNA, Neoplasm / genetics
  • Exons
  • Gene Deletion
  • Gene Expression Regulation, Neoplastic
  • Genes, Retinoblastoma / genetics*
  • Humans
  • Male
  • Molecular Sequence Data
  • Mutation*
  • Point Mutation
  • Polymerase Chain Reaction
  • Polymorphism, Single-Stranded Conformational
  • Prostate / chemistry
  • Prostate / pathology
  • Prostatic Neoplasms / chemistry
  • Prostatic Neoplasms / genetics*
  • Prostatic Neoplasms / pathology
  • RNA, Neoplasm / analysis
  • RNA, Neoplasm / chemistry
  • RNA, Neoplasm / genetics

Substances

  • DNA Primers
  • DNA, Neoplasm
  • RNA, Neoplasm