Aaptamine, a spongean alkaloid, activates p21 promoter in a p53-independent manner

Biochem Biophys Res Commun. 2006 Mar 31;342(1):101-6. doi: 10.1016/j.bbrc.2006.01.119. Epub 2006 Feb 3.

Abstract

Aaptamine, a benzonaphthyridine alkaloid was isolated from a marine sponge on the guidance of a bioassay using the transfected human osteosarcoma MG63 cells (MG63luc(+)). Aaptamine activated p21 promoter stably transfected in MG63 cells dose-dependently at the concentrations of 20-50microM. Expression of p21 and its mRNA in the wild-type MG63 cells also increased by aaptamine-treatment. Furthermore, the cell cycle of MG63 cells was arrested at the G2/M phase within 48h by the aaptamine-treatment. To analyze a responsive element of p21 promoter in the up-regulation of p21 by aaptamine, MG63 cells were transiently transfected with a series of the deleted or mutated promoter segments, and induction of luciferase with aaptamine treatment was examined by using these corresponding transfected cells. The activation of p21 promoter by aaptamine was led through acting Sp1 sites between -82 and -50bp in a p53-independent manner.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Cycle / drug effects
  • Cell Line, Tumor
  • Cyclin-Dependent Kinase Inhibitor p21 / genetics*
  • Gene Deletion
  • Gene Expression Regulation / drug effects
  • Genes, Reporter / genetics
  • Humans
  • Molecular Structure
  • Mutation / genetics
  • Naphthyridines / chemistry
  • Naphthyridines / pharmacology*
  • Porifera / chemistry*
  • Porifera / metabolism
  • Promoter Regions, Genetic / genetics*
  • RNA, Messenger / genetics
  • Tumor Suppressor Protein p53 / metabolism

Substances

  • Cyclin-Dependent Kinase Inhibitor p21
  • Naphthyridines
  • RNA, Messenger
  • Tumor Suppressor Protein p53
  • aaptamine