Department of Cell Biology, Harvard Medical School, Boston, MA 02115, USA.
Cancer Cell. 2010 Oct 19;18(4):382-95. doi: 10.1016/j.ccr.2010.08.010.
Microtubule inhibitors are important cancer drugs that induce mitotic arrest by activating the spindle assembly checkpoint (SAC), which, in turn, inhibits the ubiquitin ligase activity of the anaphase-promoting complex (APC). Here, we report a small molecule, tosyl-L-arginine methyl ester (TAME), which binds to the APC and prevents its activation by Cdc20 and Cdh1. A prodrug of TAME arrests cells in metaphase without perturbing the spindle, but nonetheless the arrest is dependent on the SAC. Metaphase arrest induced by a proteasome inhibitor is also SAC dependent, suggesting that APC-dependent proteolysis is required to inactivate the SAC. We propose that mutual antagonism between the APC and the SAC yields a positive feedback loop that amplifies the ability of TAME to induce mitotic arrest.
微管抑制剂是一类重要的抗癌药物,通过激活纺锤体组装检查点(SAC)诱导有丝分裂停滞,SAC 反过来抑制后期促进复合物(APC)的泛素连接酶活性。在这里,我们报告了一种小分子,对甲苯磺酰-L-精氨酸甲酯(TAME),它与 APC 结合,防止其被 Cdc20 和 Cdh1 激活。TAME 的前药在不扰乱纺锤体的情况下将细胞阻滞在中期,但这种阻滞仍然依赖于 SAC。蛋白酶体抑制剂诱导的中期阻滞也依赖于 SAC,这表明 APC 依赖性蛋白水解对于失活 SAC 是必需的。我们提出,APC 和 SAC 之间的相互拮抗产生了一个正反馈环,增强了 TAME 诱导有丝分裂停滞的能力。