Back to Search Start Over

UA62784 Is a cytotoxic inhibitor of microtubules, not CENP-E

Authors :
Sébastien Deshayes
Gilles Divita
Sergey Tcherniuk
Vasiliki Sarli
Ariane Abrieu
Centre de recherche en Biologie Cellulaire (CRBM)
Université Montpellier 2 - Sciences et Techniques (UM2)-Centre National de la Recherche Scientifique (CNRS)-Université de Montpellier (UM)-Université Montpellier 1 (UM1)
Source :
Chem Biol, Chem Biol, 2011, 18 (5), pp.631-41. ⟨10.1016/j.chembiol.2011.03.006⟩
Publication Year :
2011
Publisher :
HAL CCSD, 2011.

Abstract

International audience; A recent screen for compounds that selectively targeted pancreatic cancer cells isolated UA62784. We found that UA62784 inhibits microtubule polymerization in vitro. UA62784 interacts with tubulin dimers ten times more potently than colchicine, vinblastine, or nocodazole. Competition experiments revealed that UA62784 interacts with tubulin at or near the colchicine-binding site. Nanomolar doses of UA62784 promote the accumulation of mammalian cells in mitosis, due to aberrant mitotic spindles, as shown by immunofluorescence and live cell imaging. Treatment of cancerous cell lines with UA62784 is lethal, following activation of apoptosis signaling. By monitoring mitotic spindle perturbations and apoptosis, we found that the effects of UA62784 and of some known microtubule-depolymerizing drugs are additive. Finally, high content screening of H2B-GFP HeLa cells revealed that low doses of UA62784 and vinblastine potentiate each other to inhibit proliferation.

Details

Language :
English
Database :
OpenAIRE
Journal :
Chem Biol, Chem Biol, 2011, 18 (5), pp.631-41. ⟨10.1016/j.chembiol.2011.03.006⟩
Accession number :
edsair.doi.dedup.....12475817abde72f6fabf6dcaf0d6655d
Full Text :
https://doi.org/10.1016/j.chembiol.2011.03.006⟩