Overexpression of lncRNA PTENP1 suppresses glioma cell proliferation and metastasis in vitro

被引:31
作者
Hu, Su [1 ]
Xu, Li [1 ,2 ]
Li, Lihua [1 ]
Luo, Dongdong [1 ]
Zhao, Hailin [1 ]
Li, Dan [1 ]
Peng, Biao [1 ]
机构
[1] Guangzhou Med Univ, Dept Neurosurg, Affiliated Canc Hosp & Inst, 78 Heng Zhi Gang Rd, Guangzhou 510095, Guangdong, Peoples R China
[2] Cent Peoples Hosp Zhanjiang, Dept Neurosurg, Zhanjiang 524045, Guangdong, Peoples R China
来源
ONCOTARGETS AND THERAPY | 2019年 / 12卷
关键词
lncRNA PTENP1; glioma; proliferation; invasion; migration; LONG NONCODING RNAS; PSEUDOGENE; MALAT-1; CANCER; ROLES;
D O I
10.2147/OTT.S182537
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Background: Glioma is one of the most common malignancies of the central nervous system in adults. The lncRNA PTEN pseudogene-1 (PTENP1) has been reported to play an important role in the development and progression of various cancers. However, the molecular mechanism by which lncRNA PTENP1 affects the development and progression of gliomas remains unclear. Materials and methods: The levels of PTENP1 expression in glioma tissues and normal brain tissues were detected by quantitative real-time PCR. Cell Counting Kit-8 and 5-ethynyl-2'-deoxyuridine staining assays were performed to detect cell proliferation. Flow cytometry was used to analyze cell cycle progression. Transwell assay and scratch test were used to detect cell migration and invasion, and Western blot studies were performed to detect protein expression. Results: Our results showed that expression of lncRNA PTENP1 was decreased in glioma tissues when compared with normal brain tissues. Overexpression of PTENP1 suppressed SHG44 and U251 cell proliferation and significantly decreased the numbers of S-phase cells. Furthermore, the invasion and migration abilities of SHG44 and U251 cells were reduced after being transfected with a PTENP1 overexpression plasmid. Overexpression of PTENP1 induced the expression of p21 protein and suppressed the p38 signaling pathway. Conclusion: Our study investigated the function of PTENP1 in glioma and provided new insights for treating that malignancy.
引用
收藏
页码:147 / 156
页数:10
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