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Experimental Biology and Medicine 229:163-169 (2004)
© 2004 Society for Experimental Biology and Medicine


ORIGINAL RESEARCH ARTICLE

A Novel Natural Inhibitor of Extracellular Signal-Regulated Kinases and Human Breast Cancer Cell Growth

Ernest B. Izevbigie*,1, Joseph L. Bryant{dagger} and Alice Walker*

* The Molecular Genetics and Molecular & Cellular Signaling Laboratory, Department of Biology, and National Institutes of Health Center for Environmental Health, Jackson State University, Jackson, Mississippi 39217; and {dagger} Institute of Human Virology, Animal Model Division, University of Maryland Biotechnology Institute, Baltimore, Maryland 21201

To whom requests for reprints should be addressed at 1 Molecular and Cellular Signaling Laboratory, Center for Environmental Health, Jackson State University, Department of Biology, 1400 John R. Lynch Street, P.O. Box 18540, Jackson, MS 39217. E-mail: rnest.b.izevbigie{at}jsums.edu

Water-soluble extracts of edible Vernonia amygdalina leaves were recently reported as potent inhibitors of cultured MCF-7 cells. The mechanism by which V. amygdalina inhibits MCF-7 cell growth has not been previously studied. The objective of this study was to evaluate the effects of V. amygdalina on the activities, DNA synthesis, and subsequent cell growth of extracellular signal-regulated protein kinases 1 and 2 (ERKs 1/2;). Treatment of cells with various concentrations (3–100 mg/ml) of water-soluble V. amygdalina extract potently inhibited ERK activities, DNA synthesis (P < 0.005), and cell growth (P < 0.01) in a concentration-dependent fashion, both in the absence and presence of serum. The growth rate of cells pretreated with 10 mg/ml V. amygdalina for 48 hrs before transfer to V. amygdalina-free medium was not significantly different (P > 0.05) from untreated cells. These results suggest that V. amygdalina, at least at concentrations up to 10 mg/ml, exhibits cytostatic action to retard the growth of human breast cancer cells. In addition, the ERK signaling pathways may be one or more of the intracellular targets for V. amygdalina antineoplastic actions.

Key Words: human breast cancer • DNA synthesis • ERKs activities • V. amygdalina extract







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