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长链非编码RNA RP5-833A20.1通过靶向miR-18a-5p经由Akt/ERK途径抑制肝细胞癌的肿瘤发生。

Long Noncoding RNA RP5-833A20.1 Suppresses Tumorigenesis In Hepatocellular Carcinoma Through Akt/ERK Pathway By Targeting miR-18a-5p.

作者信息

Chen Zili, Ma Yifei, Pan Yaozhen, Zuo Shi, Zhu Haitao, Yu Chao, Zhu Changhao, Sun Chengyi

机构信息

Department of Hepatobiliary Surgery, Affiliated Hospital of Guizhou Medical University, Guiyang, Guizhou 550004, People's Republic of China.

Department of Otorhinolaryngology, Affiliated Hospital of Guizhou Medical University, Guiyang, Guizhou 550004, People's Republic of China.

出版信息

Onco Targets Ther. 2019 Dec 6;12:10717-10726. doi: 10.2147/OTT.S219797. eCollection 2019.

Abstract

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.

摘要

背景

先前的研究表明,长链非编码RNA(lncRNAs)在肝细胞癌(HCC)的发生发展过程中发挥着至关重要的作用。最近,在HCC组织中观察到lncRNA RP5‑833A20.1表达下调。然而,RP5‑833A20.1调控HCC细胞增殖和凋亡的潜在机制尚未得到研究。因此,本研究旨在探讨RP5‑833A20.1在HCC进展中的作用。

方法

采用RT-qPCR检测30对HCC组织及癌旁正常组织中RP5‑833A20.1的表达水平。此外,分别通过CCK-8法、流式细胞术、Transwell实验评估RP5‑833A20.1对细胞增殖、凋亡和侵袭的影响。同时,利用双荧光素酶报告系统检测HCC中RP5‑833A20.1与miR-18a-5p的相互作用。

结果

RP5‑833A20.1在HCC组织和HCC细胞系中表达显著下调。下调RP5‑833A20.1可明显促进Bel-7402细胞的增殖和侵袭。此外,过表达RP5‑833A20.1可显著抑制Huh7细胞的增殖和侵袭。而且,过表达RP5‑833A20.1可通过增加Bax和活化的caspase 3水平,降低Bcl-2、p-Akt和p-ERK水平,明显诱导Huh7细胞凋亡。同时,体内实验也表明,过表达RP5-833A20.1可抑制裸鼠皮下Huh7异种移植瘤的形成。此外,生物信息学和荧光素酶报告实验鉴定出RP5-833A20.1在HCC中作为miR-18a-5p的竞争性内源RNA(ceRNA)发挥作用。

结论

在本研究中,我们发现RP5‑833A20.1在HCC组织中表达下调。此外,RP5-833A20.1可作为miR-18a-5p的ceRNA,通过抑制Akt/ERK信号通路抑制HCC的肿瘤发生。因此,RP5-833A20.1可能是一种有价值的潜在生物标志物和HCC治疗的靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cc3c/6902849/1f5b28933227/OTT-12-10717-g0001.jpg

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