Shan Qianqian, Li Shengsheng, Cao Qiyu, Yue Chenglong, Niu Mingshan, Chen Xiangyu, Shi Lin, Li Huan, Gao Shangfeng, Liang Jun, Yu Rutong, Liu Xuejiao
Insititute of Nervous System Diseases, The Affiliated Hospital of Xuzhou Medical University, Xuzhou Medical University, Jiangsu 221002, China.
Jiangsu Key Laboratory of Bone Marrow Stem Cell, Xuzhou Medical University, Jiangsu 221002, China.
Korean J Physiol Pharmacol. 2020 May 1;24(3):193-201. doi: 10.4196/kjpp.2020.24.3.193.
Chromosomal region maintenance 1 (CRM1) is associated with an adverse prognosis in glioma. We previously reported that CRM1 inhibition suppressed glioma cell proliferation both in vitro and in vivo. In this study, we investigated the role of CRM1 in the migration and invasion of glioma cells. S109, a novel reversible selective inhibitor of CRM1, was used to treat Human glioma U87 and U251 cells. Cell migration and invasion were evaluated by wound-healing and transwell invasion assays. The results showed that S109 significantly inhibited the migration and invasion of U87 and U251 cells. However, mutation of Cys528 in CRM1 abolished the inhibitory activity of S109 in glioma cells. Furthermore, we found that S109 treatment decreased the expression level and activity of MMP2 and reduced the level of phosphorylated STAT3 but not total STAT3. Therefore, the inhibition of migration and invasion induced by S109 may be associated with the downregulation of MMP2 activity and expression, and inactivation of the STAT3 signaling pathway. These results support our previous conclusion that inhibition of CRM1 is an attractive strategy for the treatment of glioma.
染色体区域维持蛋白1(CRM1)与胶质瘤的不良预后相关。我们之前报道过,抑制CRM1可在体外和体内抑制胶质瘤细胞增殖。在本研究中,我们调查了CRM1在胶质瘤细胞迁移和侵袭中的作用。使用一种新型可逆性CRM1选择性抑制剂S109处理人胶质瘤U87和U251细胞。通过伤口愈合实验和Transwell侵袭实验评估细胞迁移和侵袭能力。结果显示,S109显著抑制U87和U251细胞的迁移和侵袭。然而,CRM1中Cys528位点的突变消除了S109对胶质瘤细胞的抑制活性。此外,我们发现S109处理降低了MMP2的表达水平和活性,并降低了磷酸化STAT3的水平,但总STAT3水平未变。因此,S109诱导的迁移和侵袭抑制可能与MMP2活性和表达的下调以及STAT3信号通路的失活有关。这些结果支持了我们之前的结论,即抑制CRM1是一种有吸引力的胶质瘤治疗策略。