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miR-141-3p suppresses proliferation and promotes apoptosis by targeting GLI2 in osteosarcoma cells
Author(s) -
Nan Wang,
Pengcheng Li,
Wei Liu,
Ningning Wang,
Zhi Lu,
Jianzhou Feng,
Xiandong Zeng,
Jiujie Yang,
Yong Wang,
Wei Zhao
Publication year - 2017
Publication title -
oncology reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.094
H-Index - 96
eISSN - 1791-2431
pISSN - 1021-335X
DOI - 10.3892/or.2017.6150
Subject(s) - osteosarcoma , gli2 , apoptosis , cancer research , oncogene , microrna , cell growth , cell cycle , biology , microbiology and biotechnology , signal transduction , hedgehog signaling pathway , gene , genetics
MicroRNAs (miRNAs) have been reported as key regulators in numerous diseases including osteosarcoma. The function of microRNA-141-3p (miR-141-3p) and whether this function is achieved by regulation of GLI family zinc finger 2 (GLI2) in osteosarcoma remain unclear. In the present study, we found decreased expression of miR-141-3p, but increased expression of GLI2 in osteosarcoma tissues and cell lines. In addition, we demonstrated a negative correlation between miR-141-3p and GLI2. Furthermore, we revealed that elevation of miR-141-3p resulted in a marked inhibition of proliferation and promotion of apoptosis as well as an obviously decrease in GLI2 in osteosarcoma cell lines. Furthermore, we determined that GLI2 is a target of miR-141-3p by a constructed luciferase assay. In addition, we showed that miR-141-3p could negatively regulate GLI2 and its downstream parathyroid hormone-related protein 1 (PTHRP1). Finally, through a series of antisense experiments we confirmed that the effect of miR-141-3p on proliferation and apoptosis was achieved through the GLI2 pathway in osteosarcoma cells. The findings of the present study may provide a new target for treating osteosarcoma.

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