Growth Attenuation in a Human Prostate Cell Line Mediated by a Phorbol Ester

Abstract Human prostatic cancer cells JCA-1 were induced with a phorbol ester 12-o-tetradecanoylphorbol-13-acetate (TPA), and cell growth differentiation were analyzed. Within hours of exposure to TPA, cell proliferation decreased and reached approximately 80% reduction after 3 days, as determined b...

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Veröffentlicht in:Experimental biology and medicine (Maywood, N.J.) N.J.), 1995-06, Vol.209 (2), p.152-156
Hauptverfasser: Novichenko, N., Konno, S., Nakajima, Y., Hsieh, T. C., Turo, W. Xu, K., Ahmed, T., Chiao, J. W.
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Sprache:eng
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Zusammenfassung:Abstract Human prostatic cancer cells JCA-1 were induced with a phorbol ester 12-o-tetradecanoylphorbol-13-acetate (TPA), and cell growth differentiation were analyzed. Within hours of exposure to TPA, cell proliferation decreased and reached approximately 80% reduction after 3 days, as determined by [3H]thymidine incorporation and cell counting. Cell cycle analysis revealed a blocking of cells entering into the replicating S and G2M phases from the G1 phase. The TPA induced cells had a reduced growth rate but remained viable. The growth-modulating activity of TPA was similarly observed with LNCaP cells. Agarose gel electrophoresis of the chromosomal DNA from induced cells exhibited a non-fragmented pattern excluding the possibility of cell apoptosis. In parallel to the growth reduction, the TPA induced cells became larger in size showing dendrite like cytoplasmic extensions. Furthermore, JCA-1 cells treated with TPA acquired the expression of cytokeratin 18 and increased the expression of actin and vimentin by 300%. These results indicate an induced growth reduction accompanied by cellular differentiation of the prostatic cancer cells.
ISSN:0037-9727
1535-3702
1535-3699
DOI:10.3181/00379727-209-43889