Department of Tumor Biology, H, Lee Moffitt Cancer Center and Research Institute, 12902 USF Magnolia Drive, Tampa, FL 33612, United States of America.
Department of Basic Sciences, Division of Pharmacology and Cancer Biology, Ponce Health Sciences University/Ponce Research Institute, Ponce 00716-2348, Puerto Rico.
Biochim Biophys Acta Mol Cell Res. 2021 Mar;1868(3):118929. doi: 10.1016/j.bbamcr.2020.118929. Epub 2020 Dec 11.
Error-free progression through mitosis is critical for proper cell division and accurate distribution of the genetic material. The anaphase-promoting complex/cyclosome (APC/C) ubiquitin ligase regulates the progression from metaphase to anaphase and its activation is controlled by the cofactors Cdc20 and Cdh1. Additionally, genome stability is maintained by the spindle assembly checkpoint (SAC), which monitors proper attachment of chromosomes to spindle microtubules prior to cell division. We had shown a role for Tank Binding Kinase 1 (TBK1) in microtubule dynamics and mitosis and here we describe a novel role of TBK1 in regulating SAC in breast and lung cancer cells. TBK1 interacts with and phosphorylates Cdc20 and Cdh1 and depletion of TBK1 elevates SAC components. TBK1 inhibition increases the association of Cdc20 with APC/C and BubR1 indicating inactivation of APC/C; similarly, interaction of Cdh1 with APC/C is also enhanced. TBK1 and TTK inhibition reduces cell viability and enhances centrosome amplification and micronucleation. These results indicate that alterations in TBK1 will impede mitotic progression and combining TBK1 inhibitors with other regulators of mitosis might be effective in eliminating cancer cells.
有丝分裂过程中无错误的进展对于细胞分裂的正常进行和遗传物质的准确分配至关重要。后期促进复合物/周期蛋白(APC/C)泛素连接酶调节从中期到后期的进展,其激活受辅助因子 Cdc20 和 Cdh1 控制。此外,纺锤体组装检查点(SAC)维持基因组稳定性,该检查点在细胞分裂之前监测染色体与纺锤体微管的正确连接。我们已经证明 Tank Binding Kinase 1 (TBK1) 在微管动力学和有丝分裂中发挥作用,在这里我们描述了 TBK1 在调节乳腺癌和肺癌细胞中的 SAC 的新作用。TBK1 与 Cdc20 和 Cdh1 相互作用并磷酸化它们,TBK1 的耗竭会增加 SAC 成分。TBK1 抑制增加了 Cdc20 与 APC/C 的结合以及 BubR1 的结合,表明 APC/C 的失活;同样,Cdh1 与 APC/C 的相互作用也得到增强。TBK1 和 TTK 抑制降低了细胞活力,并增强了中心体扩增和微核形成。这些结果表明,TBK1 的改变将阻碍有丝分裂的进展,并且将 TBK1 抑制剂与有丝分裂的其他调节剂结合可能有效消除癌细胞。