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长非编码 RNA RP5-833A20.1 通过靶向 miR-18a-5p 并经由 Akt/ERK 信号通路来抑制肝癌的肿瘤发生
Authors Chen Z, Ma Y, Pan Y, Zuo S, Zhu H, Yu C, Zhu C, Sun C
Received 17 June 2019
Accepted for publication 30 September 2019
Published 6 December 2019 Volume 2019:12 Pages 10717—10726
DOI https://doi.org/10.2147/OTT.S219797
Checked for plagiarism Yes
Review by Single-blind
Peer reviewer comments 2
Editor who approved publication: Dr Federico Perche
Background: Previous studies indicated that long noncoding RNAs (lncRNAs) played vital roles in the development and progression of hepatocellular carcinoma (HCC). Recently, downregulation of lncRNA RP5-833A20.1 has been observed in HCC tissues. However, the underlying mechanism by which RP5-833A20.1 regulates the proliferation and apoptosis in HCC has not been investigated. Thus, this study aimed to investigate the role of RP5-833A20.1 in the progression of HCC.
Methods: The levels of RP5-833A20.1 in 30 pairs of HCC tissues and adjacent normal tissues were detected by RT-qPCR. In addition, the effects of RP5-833A20.1 on cell proliferation, apoptosis and invasion were evaluated by CCK-8, flow cytometric, transwell assays, respectively. Meanwhile, the dual-luciferase reporter system assay was used to explore the interaction of RP5-833A20.1 and miR-18a-5p in HCC.
Results: The level of RP5-833A20.1 was significantly downregulated in HCC tissues and HCC cell lines. Downregulation of RP5-833A20.1 markedly promoted the proliferation and invasion of Bel-7402 cells. In addition, overexpression of RP5-833A20.1 notably inhibited the proliferation and invasion of Huh7 cells. Moreover, overexpression of RP5-833A20.1 obviously induced the apoptosis of Huh7 cells via increasing the levels of Bax and active caspase 3, and decreasing the levels of Bcl-2, p-Akt and p-ERK. Meanwhile, in vivo experiments performed also indicated that overexpression of RP5-833A20.1 could inhibit the tumorigenesis of subcutaneous Huh7 xenograft in nude mice. Furthermore, bioinformatics and luciferase reporter assay identified that RP5-833A20.1 functioned as a competing endogenous RNA (ceRNA) for miR-18a-5p in HCC.
Conclusion: In this study, we found that RP5-833A20.1 was downregulated in HCC tissues. In addition, RP5-833A20.1 could suppress the tumorigenesis in HCC through inhibiting Akt/ERK pathway by acting as a ceRNA for miR-18a-5p. Therefore, RP5-833A20.1 might be a valuable and potential biomarker and therapeutic target for the treatment of HCC.
Keywords: hepatocellular carcinoma, long noncoding RNA RP5-833A20.1, microRNA-18a-5p, proliferation
