Differential Taxol-dependent arrest of transformed and nontransformed cells in the G1 phase of the cell cycle, and specific-related mortality of transformed cells

J Cell Biol. 1996 Nov;135(3):689-700. doi: 10.1083/jcb.135.3.689.

Abstract

Taxol (paclitaxel) induces a microtubule hyperassembled state, and effectively blocks cells in mitosis. Here we report that Taxol also induces a stable late-G1 block in nontransformed REF-52 and WI-38 mammalian fibroblast cells, but not in T antigen-transformed cells of the same parental lineage. G1 arrest is characterized by partially dephosphorylated pRb, and inactive cdk2 kinase. Nontransformed cells recover normally from Taxol arrest. In contrast, T antigen transformed cells continue inappropriately past both G1 and G2-M in the presence of Taxol, and undergo a rapid death upon release. These results demonstrate a microtubule sensitive step in G1 regulation of nontransformed fibroblast cells. Also, Taxol selectively induces death of transformed cells, possibly because they slip the Taxol-dependent G1 arrest, as well as G2/M arrest, which are both specific to nontransformed cells.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antigens, Polyomavirus Transforming / physiology
  • Antineoplastic Agents, Phytogenic / pharmacology*
  • Apoptosis / drug effects
  • CDC2-CDC28 Kinases*
  • Cell Cycle Proteins*
  • Cell Line
  • Cell Line, Transformed
  • Cyclin-Dependent Kinase 2
  • Cyclin-Dependent Kinase 4
  • Cyclin-Dependent Kinase Inhibitor p21
  • Cyclin-Dependent Kinase Inhibitor p27
  • Cyclin-Dependent Kinases / analysis
  • Cyclin-Dependent Kinases / antagonists & inhibitors
  • Cyclins / analysis
  • Enzyme Inhibitors
  • Fibroblasts / cytology*
  • G1 Phase / drug effects*
  • Humans
  • Hydroxyurea / pharmacology
  • Microtubule-Associated Proteins / analysis
  • Microtubules / drug effects
  • Nocodazole / pharmacology
  • Paclitaxel / pharmacology*
  • Protein Serine-Threonine Kinases / analysis
  • Proto-Oncogene Proteins*
  • Rats
  • Retinoblastoma Protein / analysis
  • Simian virus 40 / immunology
  • Tumor Suppressor Proteins*

Substances

  • Antigens, Polyomavirus Transforming
  • Antineoplastic Agents, Phytogenic
  • CDKN1A protein, human
  • Cdkn1a protein, rat
  • Cdkn1b protein, rat
  • Cell Cycle Proteins
  • Cyclin-Dependent Kinase Inhibitor p21
  • Cyclins
  • Enzyme Inhibitors
  • Microtubule-Associated Proteins
  • Proto-Oncogene Proteins
  • Retinoblastoma Protein
  • Tumor Suppressor Proteins
  • Cyclin-Dependent Kinase Inhibitor p27
  • Protein Serine-Threonine Kinases
  • CDC2-CDC28 Kinases
  • CDK2 protein, human
  • CDK4 protein, human
  • Cdk2 protein, rat
  • Cdk4 protein, rat
  • Cyclin-Dependent Kinase 2
  • Cyclin-Dependent Kinase 4
  • Cyclin-Dependent Kinases
  • Paclitaxel
  • Nocodazole
  • Hydroxyurea