The cell cycle dependence of c-sis gene expression: artifactual conclusions in cells prepared by chemical but not physical techniques

Cell Tissue Kinet. 1990 Jul;23(4):299-312. doi: 10.1111/j.1365-2184.1990.tb01126.x.

Abstract

The c-sis oncogene encoding the B-chain of platelet-derived growth factor (PDGF) may be involved in an autocrine growth stimulation of tumours expressing the PDGF receptor, such as glioblastomas and sarcomas. To investigate whether expression of c-sis RNA is regulated in a cell cycle dependent manner, human A172 glioblastoma cells were synchronized by either centrifugal elutriation or chemical blockage with the DNA synthesis inhibitors hydroxyurea or aphidicolin. In non-perturbed elutriated cells, c-sis RNA levels were lower in the S phase of the cell cycle than in the G1 phase. In contrast, the chemically synchronized cells revealed a transient rise in c-sis RNA shortly after drug release, in early S phase. The RNA changes occurring after release from drug inhibition represent cell recovery from drug induced metabolic disturbances rather than true cell cycle dependent effects.

Publication types

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

MeSH terms

  • Aphidicolin
  • Cell Cycle / drug effects
  • Cell Cycle / genetics*
  • Centrifugation / methods
  • DNA, Neoplasm / metabolism*
  • Diterpenes / pharmacology
  • Gene Expression Regulation, Neoplastic*
  • Humans
  • Hydroxyurea / pharmacology
  • Platelet-Derived Growth Factor / genetics
  • Proto-Oncogenes / genetics*
  • RNA, Messenger / isolation & purification
  • RNA, Messenger / metabolism*
  • RNA, Neoplasm / isolation & purification
  • RNA, Neoplasm / metabolism*
  • Tumor Cells, Cultured / cytology
  • Tumor Cells, Cultured / drug effects

Substances

  • DNA, Neoplasm
  • Diterpenes
  • Platelet-Derived Growth Factor
  • RNA, Messenger
  • RNA, Neoplasm
  • Aphidicolin
  • Hydroxyurea