Expression of drug resistance-associated mdr-1, GST pi, and topoisomerase II genes during cell cycle traverse

Biochem Pharmacol. 1995 Feb 14;49(4):545-52. doi: 10.1016/0006-2952(94)00443-p.

Abstract

The expression of drug resistance-associated mdr-1, GST pi, and topoisomerase II genes was analyzed in cell cycle phase enriched populations of doxorubicin-resistant murine leukemic P388/R-84 cells. Flow cytometric analysis of bromodeoxyuridine (BrdU) incorporation and staining with anti-BrdU antibodies was used to confirm the purity of cell cycle phase enriched populations obtained by centrifugal elutriation. Doxorubicin (DOX) and daunorubicin (DNR) accumulation was significantly lower in S-phase cells, and coincubation with verapamil (VPL) or chlorpromazine (CPZ) enhanced DOX and DNR accumulation more in S-phase than in G1- and G2/M-phase cells. While the cellular content of mdr-1 and topoisomerase II mRNAs changed, GST pi mRNA content remained constant during the cell cycle. S-phase cells had about 3-fold higher mdr-1 mRNA content than G1- and G2/M-phase cells. In G1 cells, P-glycoprotein expression, as determined by C219 monoclonal antibody, was 12% less than that of S and G2/M cells. Topoisomerase II mRNA content increased with the progression of cell cycle and peaked in G2/M cells. These observations suggest that cell cycle stage related changes in expression of drug resistance markers may have a major bearing on chemosensitivity of drug-resistant cells.

Publication types

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

MeSH terms

  • ATP Binding Cassette Transporter, Subfamily B, Member 1 / analysis
  • Animals
  • Cell Cycle / genetics*
  • Cell Line / drug effects
  • Cricetinae
  • Cricetulus
  • DNA Topoisomerases, Type II / genetics*
  • Daunorubicin / pharmacology
  • Doxorubicin / pharmacology
  • Drug Resistance, Multiple / genetics*
  • Glutathione Transferase / genetics*
  • Interphase
  • Mice
  • RNA, Messenger / analysis

Substances

  • ATP Binding Cassette Transporter, Subfamily B, Member 1
  • RNA, Messenger
  • Doxorubicin
  • Glutathione Transferase
  • DNA Topoisomerases, Type II
  • Daunorubicin