期刊
CANCER CELL INTERNATIONAL
卷 18, 期 -, 页码 -出版社
BMC
DOI: 10.1186/s12935-018-0641-9
关键词
lncRNA SNHG5; miR-212-3p; Osteosarcoma; SGK3; Cell proliferation; Cell invasion and migration
类别
资金
- National Natural Science Foundation of China [81560452, 81672866]
- Natural Science Foundation of Jiangxi Province [20161BAB205192, 20171ACB21073]
- Youth Science Foundation of Jiangxi Province [20122BAB215028]
- Excellent Youth Foundation of Jiangxi Scientific Committee [20162BCB23001]
- Science and Research Fund of Jiangxi Health and Family Planning Commission [20164002]
- Foundation of Nanchang Science and Technology Bureau [2016 ZSCX009]
- Yuanhang Project of Jiangxi Province
Background: Long non-coding RNA (lncRNA) SNHG5 has been found to play an important role in tumors. Nevertheless, the function and mechanism of lncRNA SNHG5 in osteosarcoma (OS) remains unclear. The purpose of this study was to investigate whether lncRNA SNHG5 can regulate the occurrence and development of OS cells. Methods: We performed quantitative real time PCR to detect the expression of lncRNA SNHG5 in OS cells. 143B, MG63 (knockdown) and U2OS, U2R (overexpression) cell lines were chosen for the function study of SNHG5. The effect of SNHG5, miR-212-3p, and SGK3 in OS cells was explored by MTT assays, clony formation, flow cytometry, transwell assays, wound healing assays, and cell spreading assays. Quantitative real-time PCR, Western blot analysis and luciferase assays were used to detect the interaction between lncRNA SNHG5 and miR-212-3p. Results: In this study, knockdown of lncRNA SNHG5 suppressed the growth and metastasis of OS cells, whereas the overexpression of SNHG5 produced an opposite result. Mechanistically, lncRNA SNHG5 functions as a sponger against miR-212-3p and suppresses the miR-212-3p/SGK3 signaling pathway. Introduction of miR-212-3p mimics or inhibitors reverses SNHG5 overexpression or silences the exerted tumor promoting or suppressing effect. In addition, our results showed that the function of SNHG5 can be rescued by miR-212-3p and can regulate the growth and metastasis of OS cells via SGK3, the downstream target of miR-212-3p. Conclusions: In summary, our study demonstrated that lncRNA SNHG5 can regulate the proliferation and metastasis of OS cells through the miR-212-3p/SGK3 axis. This axis may provide a new target for future clinical treatment.
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