4.6 Article

(R)-roscovitine (CYC202, Seliciclib) sensitizes SH-SY5Y neuroblastorna cells to nutlin-3-induced apoptosis

Journal

EXPERIMENTAL CELL RESEARCH
Volume 312, Issue 12, Pages 2394-2400

Publisher

ELSEVIER INC
DOI: 10.1016/j.yexcr.2006.04.021

Keywords

(R)-roscovitine; CYC202; seliciclib; nuthn-3; apoptosis; p53; HDM2; cyclin; cyclin-dependent kinase; cancer

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in this study, we have analyzed the consequences, on several neuroblastoma cell lines, of combined treatments with (R)-roscovitine (CYC202, Seliciclib), a CDK inhibitory drug, and nutlin-3, a p53 activating drug. Both compounds were found to synergize, causing significant levels of apoptosis in cultured cells when combined at sublethal concentrations. In SH-SY5Y cells, Bcl-XL protein overexpression protected from apoptosis induced by either nutlin-3 alone or the (R)-roscovitine plus nutlin-3 association but failed to prevent apoptosis triggered by (R)-roscovitine alone. Moreover, Western blot studies showed that (R)-roscovitine increased nutlin-3-mediated p53 stabilization. Therefore, we conclude the contribution of (R)-roscovitine to the synergism is basically the sensitization of SH-SY5Y cells to the action of nutlin-3 on p53. The relevance of this pharmacological synergism with respect to the treatment of neuroblastoma is discussed. (c) 2006 Elsevier Inc. All rights reserved.

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