Small molecule inhibitors of cyclin-dependent kinases (CDK) have been developed as anticancer drugs with cytostatic and cytotoxic properties, but some of them have also been shown to limit angiogenesis. Here, we report that the 3,5-diaminopyrazole CAN508 inhibits endothelial cell migration and tube formation. In addition, it reduces phosphorylation of the C-terminus of RNA polymerase II and inhibits mRNA synthesis in endothelial cells, in accordance with previous observations that it has high selectivity towards the positive transcriptional regulator P-TEFb. Moreover, CAN508 reduces expression of vascular endothelial growth factor by several human cancer cell lines. The findings suggest that P-TEFb may be an attractive target for anti-angiogenic therapy.

Laboratory of Growth Regulators Faculty of Science Palacký University and Institute of Experimental Botany ASCR Šlechtitelů 11 783 71 Olomouc Czech Republic

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Modification of Boc-Protected CAN508 via Acylation and Suzuki-Miyaura Coupling

Perspective of cyclin-dependent kinase 9 (CDK9) as a drug target