Functional diversity of gro gene expression in human fibroblasts and mammary epithelial cells

Proc Natl Acad Sci U S A. 1988 Dec;85(24):9645-9. doi: 10.1073/pnas.85.24.9645.

Abstract

Previous studies of gro and related genes that are overexpressed in transformed fibroblasts suggest that gro may encode a specific growth regulator. However, DNA and protein sequence comparisons reveal relatedness to platelet factor 4 and other proteins involved in the inflammatory response. In this paper, both growth-related and cytokine-induced responses in gro gene expression are described. Human foreskin fibroblasts are shown to express approximately 10-fold elevated gro, myc, and fos mRNAs in response to serum and to phorbol 12-myristate 13-acetate stimulation, with early response kinetics indicative of growth regulation. In response to interleukin 1, however, in growing cells gro mRNA is elevated at least 100-fold but myc remains constant and fos is not expressed, suggesting a second regulatory pathway. In normal cultured mammary epithelial cells, gro is constitutively expressed, and elevated mRNA levels are induced by phorbol 12-myristate 13-acetate, but not by interleukin 1. However, most carcinoma cell lines examined do not express gro mRNA, suggesting a third function of gro as a negative growth regulator in epithelial cells.

Publication types

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

MeSH terms

  • Chromosome Banding
  • Chromosome Mapping
  • Chromosomes, Human, Pair 1*
  • Chromosomes, Human, Pair 4*
  • Cycloheximide / pharmacology
  • DNA / analysis
  • Fibroblasts / analysis
  • Fibroblasts / drug effects
  • Growth Substances / genetics*
  • Humans
  • Interleukin-1 / pharmacology
  • Oncogenes
  • Proto-Oncogenes
  • RNA, Messenger / metabolism
  • Tetradecanoylphorbol Acetate / pharmacology
  • Tumor Cells, Cultured / analysis

Substances

  • Growth Substances
  • Interleukin-1
  • RNA, Messenger
  • DNA
  • Cycloheximide
  • Tetradecanoylphorbol Acetate