Differences in kinase-mediated regulation of cell cycle progression in normal and transformed cells

• Published in: Cytometry (Baltimore); (United States) Vol. 6
• Main Authors: Crissman, H.A., Gadbois, D.M., Tobey, R.A., Stevenson, A.P., Kraemer, P.M., Bustos, L.D., Dickson, J.A., Bradbury, E.M.
• Format: Conference Proceeding
• Language: English
• Published: United States 01.01.1993
• Subjects: 550200 > Biochemistry; BASIC BIOLOGICAL SCIENCES; CELL PROLIFERATION; CELL TRANSFORMATIONS; CONTROL; DNA REPLICATION; ENZYME INHIBITORS; ENZYMES; NUCLEIC ACID REPLICATION; ONCOGENIC TRANSFORMATIONS; ORGANIC COMPOUNDS; PHOSPHORUS-GROUP TRANSFERASES; PHOSPHOTRANSFERASES; PROTEINS; QUANTITY RATIO; TRANSFERASES 550300 > Cytology
• ISSN: 0196-4763; 1097-0320

Staurosporine (Stsp), a general protein kinase inhibitor, was used to investigate the role of kinase-mediated mechanisms in regulating mammalian cell proliferation. Low levels of Stsp (1-2nM) prevented nontransformed cells from entering S phase, indicating that protein phosphorylation processes are essential for commitment of DNA replication in normal cells. Cells resumed cycling when Stsp was removed. The period of sensitivity of nontransformed human diploid fibroblasts to low levels of the drug commenced 3 h later than the G0/G1 boundary and extended through the G1/S boundary. The initial block point at 3 h corresponds neither to the serum nor the amino acid restriction point. In contrast, neither low nor high concentrations (100nm) of Stsp affected G1 progression of transformed cells. High drug concentrations blocked normal cells in G1 and G2 but affected only G2-progression in transformed cells. These results indicate that kinase-mediated regulation of DNA replication is lost as a result of neoplastic transformation, but the G2-arrest mechanism remains intact.