RETRACTED: |MicroRNA-203 inhibits the proliferation and invasion of U251 glioblastoma cells by directly targeting PLD2 (Retracted Article)

被引:50
作者
Chen, Zigui [1 ]
Li, Dazhi [2 ]
Cheng, Quan [1 ]
Ma, Zhiming [1 ]
Jiang, Bing [1 ]
Peng, Renjun [1 ]
Chen, Rui [1 ]
Cao, Yiqiang [1 ]
Wan, Xin [1 ]
机构
[1] Cent South Univ, Xiangya Hosp 1, Dept Neurosurg, Changsha 410008, Hunan, Peoples R China
[2] Xinjiang Med Univ, Tradit Chinese Med Hosp, Dept Neurosurg, Urumqi 830000, Xinjiang, Peoples R China
关键词
glioma; glioblastoma; microRNA-203; phospholipase D2; proliferation; invasion; PHOSPHOLIPASE-D; DOWN-REGULATION; EXPRESSION; MICRORNAS; MIGRATION; ACTIVATION; PROGNOSIS; CARCINOMA; MIR-203; PROTEIN;
D O I
10.3892/mmr.2013.1814
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
MicroRNAs (miRNAs) have been demonstrated to be important in the development and progression of various types of cancer. However, the exact roles of certain anti-oncogenic miRNAs in human malignant gliomas remain to be elucidated. The present study aimed to reveal the expression of microRNA-203 (miR-203) in normal brain tissues and gliomas, and to investigate the role of miR-203 in cell proliferation and migration in human glioblastoma U251 cells. Real-time reverse transcription polymerase chain reaction (RT-PCR) showed that the expression of miR-203 in high WHO grade glioma tissues was significantly decreased compared with low WHO grade glioma tissues and normal brain tissues, and its expression demonstrated a decreasing tendency with ascending WHO grades. The transfection of the miR-203 mimic into U251 cells markedly downregulated the expression of phospholipase D2 (PLD2), which was identified as a direct target of miR-203. Furthermore, miR-203 overexpression significantly suppressed the proliferation and invasion of U251 cells, while the overexpression of PLD2 abrogated these effects induced by the miR-203 mimic. In conclusion, the present study demonstrated the clinical significance of miR-203 in gliomas and suggested that miR-203 was able to inhibit the proliferation and invasion of glioma cells, partially at least via suppressing the protein expression of PLD2. Thus, miR-203 may be a novel candidate for the development of therapeutic strategies for gliomas.
引用
收藏
页码:503 / 508
页数:6
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