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长链非编码RNA HOXA-AS2通过靶向miR-145-3p在人类非小细胞肺癌中发挥癌基因作用。

Long noncoding RNA HOXA-AS2 acts as an oncogene by targeting miR-145-3p in human non-small cell lung cancer.

作者信息

Shi Y-B, Liu S-L, Mou X-R, Liao J, Che J-P, Fei X-Q, Wang A-R

机构信息

Department of Cardiothoracic Surgery, Yantai Mountain Hospital, Yantai, China.

出版信息

Eur Rev Med Pharmacol Sci. 2020 Feb;24(3):1243-1249. doi: 10.26355/eurrev_202002_20177.

DOI:10.26355/eurrev_202002_20177
PMID:32096154
Abstract

OBJECTIVE

Recent studies have proved that long non-coding RNAs (lncRNAs) play important roles in many diseases, especially malignancies. The aim of this study was to investigate the exact role of lncRNA HOXA-AS2 (Hoxa cluster antisense RNA 2) in the development of non-small cell lung cancer (NSCLC).

PATIENTS AND METHODS

Quantitative Real Time-Polymerase Chain Reaction (qRT-PCR) was utilized to detect HOXA-AS2 expression in NSCLC patients. The Wound healing assay and transwell assay were conducted to explore the function of HOXA-AS2 on NSCLC metastasis. Furthermore, the mechanism assays were used to explore the interaction between HOXA-AS2 and microRNA-145-3p (miR-145-3p).

RESULTS

HOXA-AS2 expression level in NSCLC tissues was significantly higher than adjacent tissues. HOXA-AS2 expression was negatively correlated with disease-free survival of NSCLC patients. Moreover, the functional assays showed that the migration and invasion of NSCLC cells were significantly inhibited after HOXA-AS2 in vitro silence. Furthermore, the luciferase reporter gene assay also revealed that miR-145-3p was a direct target of HOXA-AS2 in NSCLC.

CONCLUSIONS

Our results indicated that HOXA-AS2 could enhance the migration and invasion abilities of NSCLC by targeting miR-145-3p. Furthermore, these findings suggested that HOXA-AS2 might be a potential therapeutic target for NSCLC.

摘要

目的

近期研究已证明长链非编码RNA(lncRNAs)在许多疾病尤其是恶性肿瘤中发挥重要作用。本研究旨在探讨长链非编码RNA HOXA-AS2(Hoxa簇反义RNA 2)在非小细胞肺癌(NSCLC)发生发展中的具体作用。

患者与方法

采用定量实时聚合酶链反应(qRT-PCR)检测NSCLC患者中HOXA-AS2的表达。进行伤口愈合试验和Transwell试验以探究HOXA-AS2对NSCLC转移的作用。此外,运用机制分析来探究HOXA-AS2与微小RNA-145-3p(miR-145-3p)之间的相互作用。

结果

NSCLC组织中HOXA-AS2表达水平显著高于癌旁组织。HOXA-AS2表达与NSCLC患者无病生存期呈负相关。此外,功能试验表明HOXA-AS2体外沉默后NSCLC细胞的迁移和侵袭能力显著受到抑制。而且,荧光素酶报告基因试验还显示miR-145-3p是NSCLC中HOXA-AS2的直接靶点。

结论

我们的结果表明HOXA-AS2可通过靶向miR-145-3p增强NSCLC的迁移和侵袭能力。此外,这些发现提示HOXA-AS2可能是NSCLC的一个潜在治疗靶点。

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