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miR-218 expression in osteosarcoma tissues and its effect on cell growth in osteosarcoma cells.

Authors :
Wang HT
Liu AG
Luo DS
Zhou ZN
Lin HG
Chen RZ
He JS
Chen K
Source :
Asian Pacific journal of tropical medicine [Asian Pac J Trop Med] 2014 Dec; Vol. 7 (12), pp. 1000-4.
Publication Year :
2014

Abstract

Objective: To investigate the expression of miR-218 and its clinical significance in osteosarcoma tissues and explore its effect on proliferation and apoptosis in osteosarcoma cells.<br />Methods: miR-218 expression was detected in 76 samples of surgically resected osteosarcoma and matched normal tumor-adjacent tissues using quantitative reverse transcription polymerase chain reaction (qRT-PCR). MiR-218 was over-expressed by exogenous miR-218 plasmids in Saos-2 cells, and then BrdU cell proliferation assay and flow cytometry were used to determine cell proliferation and apoptosis.<br />Results: The expression of miR-218 in osteosarcoma tissues was significantly lower than those in normal tumor-adjacent tissues (t=8.735, P<0.001). MiR-218 expression in tumor tissues was significantly correlated with tumor size (χ(2)=5.380, P=0.020), clinical stage (χ(2)=6.692, P=0.010) and distant metastasis (χ(2)=4.180, P=0.041). MiR-218 was obviously over-expressed by exogenous miR-218 plasmids (t=19.42, P<0.001), and miR-218 overexpression significantly reduced cell proliferation (t=9.045, P<0.001) and induced apoptosis (t=12.38, P<0.001) in Saos-2 cells.<br />Conclusions: The low-expression of miR-218 is correlated with the poor clinicopathological features in osteosarcoma. Moreover, miR-218 overexpression reduces cancer cell proliferation and induces apoptosis in Saos-2 cells, suggesting that miR-218 may play a key role in the progression of human osteosarcoma.<br /> (Copyright © 2014 Hainan Medical College. Published by Elsevier B.V. All rights reserved.)

Details

Language :
English
ISSN :
2352-4146
Volume :
7
Issue :
12
Database :
MEDLINE
Journal :
Asian Pacific journal of tropical medicine
Publication Type :
Academic Journal
Accession number :
25479631
Full Text :
https://doi.org/10.1016/S1995-7645(14)60176-0