Inhibition of chromosomal region maintenance 1 suppresses the migration and invasion of glioma cells via inactivation of the STAT3/MMP2 signaling pathway

被引:2
|
作者
Shan, Qianqian [1 ]
Li, Shengsheng [1 ]
Cao, Qiyu [1 ]
Yue, Chenglong [1 ]
Niu, Mingshan [1 ,2 ]
Chen, Xiangyu [1 ]
Shi, Lin [1 ]
Li, Huan [1 ]
Gao, Shangfeng [1 ,3 ]
Liang, Jun [3 ]
Yu, Rutong [1 ,3 ]
Liu, Xuejiao [1 ,3 ]
机构
[1] Xuzhou Med Univ, Affiliated Hosp, Inst Nervous Syst Dis, Xuzhou 221002, Jiangsu, Peoples R China
[2] Xuzhou Med Univ, Jiangsu Key Lab Bone Marrow Stem Cell, Xuzhou 221002, Jiangsu, Peoples R China
[3] Xuzhou Med Univ, Dept Neurosurg, Affiliated Hosp, Xuzhou 221002, Jiangsu, Peoples R China
来源
KOREAN JOURNAL OF PHYSIOLOGY & PHARMACOLOGY | 2020年 / 24卷 / 03期
基金
中国国家自然科学基金;
关键词
Glioma; Invasion; Migration; S109; STAT3/MMP2; signaling; NUCLEAR EXPORT; HIGH EXPRESSION; CRM1; ACTIVATION; CANCER; PROGNOSIS; PROLIFERATION; TRANSCRIPTION; INFLAMMATION; PROGRESSION;
D O I
10.4196/kjpp.2020.24.3.193
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
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.
引用
收藏
页码:193 / 201
页数:9
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