Wu Zhen Hua, Hu Long Yu, Xu Da Qian, Li Xiaotong
School of Life Sciences, Xiamen University, Xiamen, Fujian, P.R. China.
Assay Drug Dev Technol. 2012 Aug;10(4):344-52. doi: 10.1089/adt.2011.416. Epub 2012 Feb 21.
In eukaryotes, the spindle checkpoint acts as a surveillance mechanism that ensures faithful chromosome segregation. The spindle checkpoint prevents premature separation of sister chromatids and the onset of anaphase until every chromosome is properly attached to the mitotic spindle. Tumorigenesis might result from generation of aneuploidy by dysfunction of the spindle checkpoint. Differences of the checkpoint system in normal cells versus tumor cells might provide a new opportunity in cancer drug development; therefore, efforts to identify the spindle checkpoint inhibitors have been fostered. Based on spindle checkpoint inhibitors being able to induce cells to exit mitotic arrest caused by microtubule drug treatment, we developed a cell-based assay to screen compounds that were potential spindle checkpoint inhibitors. This assay was validated with a known spindle checkpoint inhibitor and was easy to adapt to a large-scale screening. It also had the advantages of being high in sensitivity and low in cost.
在真核生物中,纺锤体检查点作为一种监测机制,确保染色体准确分离。纺锤体检查点可防止姐妹染色单体过早分离以及后期的开始,直到每条染色体都正确地附着在有丝分裂纺锤体上。肿瘤发生可能是由于纺锤体检查点功能障碍导致非整倍体的产生。正常细胞与肿瘤细胞中检查点系统的差异可能为癌症药物开发提供新的机会;因此,人们一直在努力寻找纺锤体检查点抑制剂。基于纺锤体检查点抑制剂能够诱导细胞退出由微管药物处理引起的有丝分裂停滞,我们开发了一种基于细胞的检测方法来筛选潜在的纺锤体检查点抑制剂化合物。该检测方法已用一种已知的纺锤体检查点抑制剂进行了验证,并且易于适应大规模筛选。它还具有灵敏度高和成本低的优点。