LIM domain only 2 induces glioma invasion via cytosolic p27KIP1

被引:4
作者
Park, Cheol Gyu [1 ]
Sohn, Young-Woo [1 ]
Kim, Eun-Jung [1 ,2 ]
Kim, Sung-Hak [1 ,3 ]
Kim, Sung-Chan [4 ]
Kim, Hyunggee [1 ,2 ]
机构
[1] Korea Univ, Dept Biotechnol, Sch Life Sci & Biotechnol, Seoul 136713, South Korea
[2] Korea Univ, Inst Anim Mol Biotechnol, Seoul 136713, South Korea
[3] Ohio State Univ, James Comprehens Canc Ctr, Dept Neurol Surg, Columbus, OH 43210 USA
[4] Hallym Univ, Coll Med, Dept Biochem, Chunchon 200702, South Korea
基金
新加坡国家研究基金会;
关键词
Cell invasion; Cell migration; Glioma; LMO2; p27(Kip1); RhoA; KINASE INHIBITOR P27(KIP1); CELL-CYCLE PROGRESSION; BREAST-CANCER; PHOSPHORYLATION; EXPRESSION; MIGRATION; PROTEINS; LMO2; LOCALIZATION; GLIOBLASTOMA;
D O I
10.1007/s13277-015-4072-0
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
High-grade gliomas are considered the most malignant of brain tumors and have a poor prognosis. In a previous study, we showed that LIM domain only 2 (LMO2) regulates glioma stem cell properties and tumor angiogenesis and gave rise to highly invasive glioma xenografts. Glioma invasion in the surrounding parenchymal tissues is a major hurdle with respect to eliminating glioma by surgery. Invasive glioma cells are considered one of the main culprits for the recurrence of tumors after therapies. In the current study, we focused on determining the molecular mechanism(s) by which LMO2 regulates glioma cell migration and invasion. Forced expression of LMO2 in human U87MG glioma cells led to glioma invasion, as determined by in vivo xenograft assays and enhanced in vitro migration and invasion. LMO2 was associated with increased levels of cytosolic p27(Kip1) protein. LMO2 possibly induced the stabilization and augmented interactions between p27(Kip1) and RhoA. We knocked down the expression of p27(Kip1), which led to a decrease in LMO2-driven glioma cell migration and invasion. Taken together, our findings indicate that LMO2 promotes glioma cell migration and invasion by increasing the levels of cytosolic p27(Kip1).
引用
收藏
页码:2473 / 2480
页数:8
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