Mitotic catastrophe and apoptosis induced by docetaxel in hormone-refractory prostate cancer cells.

Francesco Fabbri, Dino Amadori, Silvia Carloni, Giovanni Brigliadori, Anna Tesei, Paola Ulivi, Marco Rosetti, Ivan Vannini, Chiara Arienti, Wainer Zoli, Rosella Silvestrini

Journal: Journal of cellular physiology 2008;217(2):494-501

PMID: 18615564

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Abstract

Studies performed in different experimental and clinical settings have shown that Docetaxel (Doc) is effective in a wide range of tumors and that it exerts its activity through multiple mechanisms of action. However, the sequence of events induced by Doc which leads to cell death is still not fully understood. Moreover, it is not completely clear how Doc induces mitotic catastrophe and whether this process is an end event or followed by apoptosis or necrosis. We investigated the mechanisms by which Doc triggers cell death in hormone-refractory prostate cancer cells by analyzing cell cycle perturbations, apoptosis-related marker expression, and morphologic cell alterations. Doc induced a transient increase in G2/M phase followed by the appearance of G0/1 hypo- and hyperdiploid cells and increased p21 expression. Time- and concentration-dependent apoptosis was induced in up to 70% of cells, in concomitance with Bcl-2 phosphorylation, which was followed by caspase-2 and -3 activation. In conclusion, Doc would seem to trigger apoptosis in hormone-refractory prostate cancer cells via mitotic catastrophe through two forms of mitotic exit, in concomitance with increased p21 expression and caspase-2 activation.

Address: Istituto Scientifico Romagnolo per lo Studio e la Cura dei Tumori (I.R.S.T.), Meldola (FC), Italy.

DOI: 10.1002/jcp.21522