RRC ID 39533
Author Fukumi S, Horiguchi-Yamada J, Iwase S, Ohno T, Yamada H.
Title Concentration-dependent variable effects of etoposide on the cell cycle of CML cells.
Journal Anticancer Res
Abstract BACKGROUND:Etoposide, a DNA-topoisomerase II inhibitor, is used for a broad spectrum of cancers with various therapeutic strategies. But the molecular mechanisms of its concentration-dependent effects are not clearly defined.
MATERIALS AND METHODS:Chronic myelogenous leukemia K562 cells were treated with low (5 microM) or high (100 microM) concentrations of this drug and the changes of cell cycle progression, expression of cell cycle regulating genes and cyclin B1-dependent histone H1 kinase activity were studied.
RESULTS:In the presence of 5 microM etoposide, K562 cells continued to synthesize DNA and most cells showed progress into G2 phase until 24 hours. In contrast, 100 microM etoposide rapidly inhibited DNA synthesis by around 6 hours and most cells remained in their initial phase, while the incorporation of bromodeoxyuridine was partially resumed from 12 hours. The histone H1 kinase activity was only down-regulated in the early phase of 100 microM treated cells. Among the cell cycle controlling genes, c-Myc and P21Cip1/WAF1 showed impressive responses to the two etoposide concentrations. At 100 microM, c-Myc protein rapidly vanished at 3 hours, while p21Cip1/WAF1 was inversely induced from 3 hours. These changes were also observed at 5 microM, but they occurred slowly and weakly.
CONCLUSION:The present findings indicate that two concentrations of etoposide functioned as an anticancer agent through modulating the genes related in cell cycle progression. Differing responses of c-Myc and p21Cip1/WAF1 at two concentrations may govern the antiproliferative effects of etoposide.
Volume 20(5A)
Pages 3105-10
Published 2000-1-1
PMID 11062729
MeSH Antineoplastic Agents, Phytogenic / pharmacology* Cell Cycle / drug effects* Cyclin B / metabolism Cyclin B1 Dose-Response Relationship, Drug Etoposide / pharmacology* Gene Expression Regulation / drug effects Humans K562 Cells Leukemia, Myelogenous, Chronic, BCR-ABL Positive Nucleic Acid Synthesis Inhibitors / pharmacology* Protein Kinases / metabolism Topoisomerase II Inhibitors*
IF 1.994
Times Cited 5
WOS Category ONCOLOGY
Resource
Human and Animal Cells