Induction of HSP70 gene expression by the antiproliferative prostaglandin PGA2: a growth-dependent response mediated by activation of heat shock transcription factor. Academic Article uri icon

Overview

MeSH

  • Cell Division
  • Culture Media
  • Cycloheximide
  • HeLa Cells
  • Humans
  • Promoter Regions, Genetic
  • Protein Biosynthesis
  • Transcription, Genetic

MeSH Major

  • Gene Expression Regulation
  • Heat-Shock Proteins
  • Prostaglandins A
  • RNA, Messenger
  • Transcription Factors

abstract

  • Prostaglandins (PG) of the A series are potent inhibitors of cell proliferation. Recently, it was shown that PGA2-induced growth arrest was associated with the increased synthesis of stress proteins encoded by the HSP70 gene family. In this study, we have examined the molecular basis for this increases HSP70 expression. Northern (RNA) blot analysis and nuclear run-on assays demonstrated that induction of high levels of HSP70 mRNA results from an increase in the rate of transcription. High-level induction is specific to the HSP70 family of heat shock proteins and is rapid, reversible, dose dependent, and specific for PGs capable of growth-arresting HeLa cells. In addition, the response was found to be highly dependent on the growth state of the cells, as induction occurs in growing but not in confluent nongrowing cell populations. Induction is dependent on the activation of heat shock factor. Cycloheximide pretreatment, which inhibits the antiproliferative effects of PGA2, prevents activation of the heat shock factor and induction of HSP70 mRNA by PGA2. These results support a role for HSP70 in mediating the antiproliferative effects of PGA2.

publication date

  • April 1992

has subject area

  • Cell Division
  • Culture Media
  • Cycloheximide
  • Gene Expression Regulation
  • HeLa Cells
  • Heat-Shock Proteins
  • Humans
  • Promoter Regions, Genetic
  • Prostaglandins A
  • Protein Biosynthesis
  • RNA, Messenger
  • Transcription Factors
  • Transcription, Genetic

Research

keywords

  • Journal Article

Identity

Language

  • eng

PubMed Central ID

  • PMC369594

PubMed ID

  • 1549109

Additional Document Info

start page

  • 1528

end page

  • 1534

volume

  • 12

number

  • 4