Gurgis Fms, Åkerfeldt M C, Heng B, Wong C, Adams S, Guillemin G J, Johns T G, Chircop M, Munoz L
School of Medical Sciences, Department of Pharmacology, The University of Sydney , Sydney, NSW 2006, Australia.
Faculty of Medicine and Health Sciences, Macquarie University , NSW 2109, Australia.
Cell Death Discov. 2015 Sep 7;1:15028. doi: 10.1038/cddiscovery.2015.28. eCollection 2015.
MAPK-activated protein kinase 2 (MK2) is a checkpoint kinase involved in the DNA damage response. MK2 inhibition enhances the efficacy of chemotherapeutic agents; however, whether MK2 inhibition alone, without concurrent chemotherapy, would attenuate survival of cancer cells has not been investigated. CMPD1 is a widely used non-ATP competitive inhibitor that prevents MK2 phosphorylation. We employed CMPD1 together with MK2 knock-down and ATP-competitive MK2 inhibitor III (MK2i) in a panel of glioblastoma cells to assess whether MK2 inhibition could induce cancer cell death. While CMPD1 was effective at selective killing of cancer cells, MK2i and MK2 knock-down had no effect on viability of glioblastoma cells. CMPD1 treatment induced a significant G2/M arrest but MK2i-treated cells were only minimally arrested at G1 phase. Intriguingly, at doses that were cytotoxic to glioblastoma cells, CMPD1 did not inhibit phosphorylation of MK2 and of its downstream substrate Hsp27. These results suggest that CMPD1 exhibits cytotoxic activity independently of MK2 inhibition. Indeed, we identified tubulin as a primary target of the CMPD1 cytotoxic activity. This study demonstrates how functional and mechanistic studies with appropriate selection of test compounds, combining genetic knock-down and pharmacological inhibition, coordinating timing and dose levels enabled us to uncover the primary target of an MK2 inhibitor commonly used in the research community. Tubulin is emerging as one of the most common non-kinase targets for kinase inhibitors and we propose that potential tubulin-targeting activity should be assessed in preclinical pharmacology studies of all novel kinase inhibitors.
丝裂原活化蛋白激酶2(MK2)是一种参与DNA损伤反应的检查点激酶。抑制MK2可增强化疗药物的疗效;然而,单独抑制MK2(不联合化疗)是否会削弱癌细胞的存活能力尚未得到研究。CMPD1是一种广泛使用的非ATP竞争性抑制剂,可阻止MK2磷酸化。我们在一组胶质母细胞瘤细胞中使用CMPD1,同时敲低MK2并使用ATP竞争性MK2抑制剂III(MK2i),以评估抑制MK2是否能诱导癌细胞死亡。虽然CMPD1能有效选择性杀死癌细胞,但MK2i和敲低MK2对胶质母细胞瘤细胞的活力没有影响。CMPD1处理可诱导显著的G2/M期阻滞,但MK2i处理的细胞仅在G1期有轻微阻滞。有趣的是,在对胶质母细胞瘤细胞具有细胞毒性的剂量下,CMPD1并未抑制MK2及其下游底物Hsp27的磷酸化。这些结果表明,CMPD1表现出独立于MK2抑制的细胞毒性活性。事实上,我们确定微管蛋白是CMPD1细胞毒性活性的主要靶点。这项研究展示了如何通过适当选择测试化合物进行功能和机制研究,结合基因敲低和药理学抑制,协调时间和剂量水平,使我们能够揭示研究界常用的一种MK2抑制剂的主要靶点。微管蛋白正成为激酶抑制剂最常见的非激酶靶点之一,我们建议在所有新型激酶抑制剂的临床前药理学研究中评估潜在的微管蛋白靶向活性。