Expression of a dominant negative heat shock factor-1 construct inhibits aneuploidy in prostate carcinoma cells

J Biol Chem. 2004 Jul 30;279(31):32651-9. doi: 10.1074/jbc.M401475200. Epub 2004 May 19.

Abstract

Recent studies have implicated heat shock proteins (HSP) and heat shock transcription factor 1 (HSF1) in tumor progression. We have examined the role of HSF1 in the malignant phenotype of PC-3 prostate carcinoma cells. We have developed a dominant negative construct of HSF1 that antagonizes transcription from HSP promoters and results in the depletion of intracellular HSP 70. Our studies indicate that expression of DN-HSF1 dramatically alters the DNA content of PC-3 cells (derived from p53 null prostatic carcinoma) and inhibits aneuploidy in these cells. This effect is due to prolonged expression of DN-HSF1, and transient expression of the dominant negative factor from an inducible promoter failed to cause the effect. Inhibition of aneuploidy in p53 null PC-3 cells by DN-HSF1 expression was recapitulated by expression within the cells of wild type p53. Furthermore, cells expressing DN-HSF1 showed a profound inhibition in the development of aneuploidy when exposed to chemical agents that disrupt the mitotic spindle and prevent progression through metaphase. Inhibition of aneuploidy in PC-3 cells expressing DN-HSF1 was associated with delayed breakdown of cyclin B1 compared with controls, consistent with a role for wild type HSF1 in the regulation of cyclin B1 degradation, a key step in the control of mitosis. Our experiments therefore demonstrate that HSF1 plays a functional role in cancer cells under nonstress conditions and influences cell cycle behavior and progression through mitosis and promotes the development of the aneuploid state.

Publication types

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

MeSH terms

  • Aneuploidy*
  • Antineoplastic Agents, Phytogenic / pharmacology
  • Cell Cycle
  • Cell Division
  • Cell Line
  • Cell Line, Tumor
  • Cells, Cultured
  • Cyclin B / metabolism
  • Cyclin B1
  • DNA / metabolism
  • DNA-Binding Proteins / genetics*
  • Demecolcine / pharmacology
  • Dose-Response Relationship, Drug
  • Electrophoresis, Polyacrylamide Gel
  • Genes, Dominant*
  • Genes, Reporter
  • Genes, p53
  • Genetic Vectors
  • HSP72 Heat-Shock Proteins
  • Heat Shock Transcription Factors
  • Heat-Shock Proteins / metabolism
  • Humans
  • Immunoblotting
  • Luciferases / metabolism
  • Male
  • Mitosis
  • Mutation
  • Phenotype
  • Ploidies
  • Promoter Regions, Genetic
  • Prostatic Neoplasms / genetics*
  • Protein Structure, Tertiary
  • Resting Phase, Cell Cycle
  • Spectrometry, Fluorescence
  • Transcription Factors
  • Transfection

Substances

  • Antineoplastic Agents, Phytogenic
  • CCNB1 protein, human
  • Cyclin B
  • Cyclin B1
  • DNA-Binding Proteins
  • HSF1 protein, human
  • HSP72 Heat-Shock Proteins
  • Heat Shock Transcription Factors
  • Heat-Shock Proteins
  • Transcription Factors
  • DNA
  • Luciferases
  • Demecolcine