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Research Articles: Therapeutics, Targets, and Development

Cell type–dependent effects of Polo-like kinase 1 inhibition compared with targeted polo box interference in cancer cell lines

Nycomed GmbH, Konstanz, Germany

Requests for reprints: Mathias Schmidt, Nycomed GmbH, RPD/SO, Byk-Gulden-Strasse 2, D-78467 Konstanz, Germany. Phone: 49-7531-842945; Fax: 49-7531-8492945. E-mail: mathias.schmidt{at}nycomed.com

Abstract

Multiple critical roles within mitosis have been assigned to Polo-like kinase 1 (Plk1), making it an attractive candidate for mitotic targeting of cancer cells. Plk1 contains two domains amenable for targeted interference: a kinase domain responsible for the enzymatic function and a polo box domain necessary for substrate recognition and subcellular localization. Here, we compare two approaches for targeted interference with Plk1 function, either by a Plk1 small-molecule enzyme inhibitor or by inducible overexpression of the polo box in human cancer cell lines. Inducible expression of the Plk1 polo box resulted in growth inhibition of RKOp27 human colon adenocarcinoma cells without obvious signs of mitotic abnormalities. A Plk1 kinase inhibitor in the same cell line arrested cells in mitosis with subsequent onset of apoptosis. Similarly, PC-3 human prostate cancer cells were growth inhibited on expression of the polo box. Prolonged expression of the polo box in these cells resulted in the occurrence of binucleated or multinucleated cells. In contrast, U2OS human osteosarcoma cells responded to overexpression of the polo box with a massive mitotic accumulation coinciding with the onset of apoptosis. Comparison of spindle formation revealed very similar mitotic abnormalities in polo box–overexpressing U2OS cells compared with U2OS cells treated with the Plk1 kinase inhibitor. We conclude that interference with polo box function and inhibition of Plk1 kinase activity can exert very similar phenotypic effects in certain cell lines but highly contrasting effects in others. This may point to subtle differences in the molecular machinery of mitosis regulation in cancer cells. [Mol Cancer Ther 2007;6(12):3189–97]

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Note: Current address for J. Fink: Institut Curie, Centre National de la Recherche Scientifique, Unité Mixte de Recherche 144, 26 rue d'Ulm, 75248 Paris, France. Current address for T.L. Beckers: Oncotest GmbH, am Flughafen 12-14, D-79108 Freiburg, Germany.

¹ Supplementary material for this article is available at Molecular Cancer Therapeutics Online (http://mct.aacrjournals.org/).

Received 1/23/07; revised 8/16/07; accepted 10/ 9/07.