Insulin induces PFKFB3 gene expression in HT29 human colon adenocarcinoma cells

Biochim Biophys Acta. 2002 Apr 3;1589(2):89-92. doi: 10.1016/s0167-4889(02)00169-6.

Abstract

Fructose 2,6-bisphosphate is present at high concentrations in many established lines of transformed cells. It plays a key role in the maintenance of a high glycolytic rate by coupling hormonal and growth factor signals with metabolic demand. The concentration of fructose 2,6-bisphosphate is controlled by the activity of the homodimeric bifunctional enzyme 6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase (PFK-2). We report here the PFKFB-3 gene expression control by insulin in the human colon adenocarcinoma HT29 cell line. The incubation of these cells with 1 microM insulin resulted in an increase in the PFK-2 mRNA level after 6 h of treatment, this effect being blocked by actinomycin D. Furthermore, insulin induced ubiquitous PFK-2 protein levels, that were evident after a lag of 3 h and could be inhibited by incubation with cycloheximide.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cycloheximide / pharmacology
  • Dactinomycin / pharmacology
  • Gene Expression Regulation / drug effects
  • Glycolysis
  • HT29 Cells
  • Humans
  • Insulin / pharmacology*
  • Phosphofructokinase-2 / antagonists & inhibitors
  • Phosphofructokinase-2 / metabolism
  • Protein Biosynthesis*
  • Proteins*
  • RNA, Messenger / analysis
  • RNA, Messenger / metabolism
  • Time Factors

Substances

  • Insulin
  • Proteins
  • RNA, Messenger
  • Dactinomycin
  • Cycloheximide
  • PFKFB3 protein, human
  • Phosphofructokinase-2