Tcherniuk Sergey, Deshayes Sébastien, Sarli Vasiliki, Divita Gilles, Abrieu Ariane
Université de Montpellier Sud de France, CRBM, Montpellier, France.
Chem Biol. 2011 May 27;18(5):631-41. doi: 10.1016/j.chembiol.2011.03.006.
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.
最近对选择性靶向胰腺癌细胞的化合物进行的筛选分离出了UA62784。我们发现UA62784在体外抑制微管聚合。UA62784与微管蛋白二聚体的相互作用比秋水仙碱、长春碱或诺考达唑强十倍。竞争实验表明,UA62784在秋水仙碱结合位点或其附近与微管蛋白相互作用。如免疫荧光和活细胞成像所示,纳摩尔剂量的UA62784由于异常有丝分裂纺锤体而促进哺乳动物细胞在有丝分裂期的积累。用UA62784处理癌细胞系会在凋亡信号激活后导致细胞死亡。通过监测有丝分裂纺锤体扰动和凋亡,我们发现UA62784与一些已知的微管解聚药物的作用是相加的。最后,对H2B-GFP HeLa细胞进行的高内涵筛选表明,低剂量的UA62784和长春碱相互增强以抑制增殖。