Cell cycle-independent induction of apop
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Sabine Brüsselbach; Dirk M. Nettelbeck; Hans-Harald Sedlacek; Rolf Müller
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Article
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1998
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John Wiley and Sons
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French
⚖ 173 KB
👁 2 views
The anti-tumor drug Flavopiridol is a potent inhibitor of cyclin-dependent kinases (cdks). As a consequence, Flavopiridol-treated cells arrest in both G1 and G2, but Flavopiridol has also been shown to be cytotoxic for some tumor cell lines. The underlying molecular events are, however, unclear. We