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长链非编码RNA ROR1-AS1通过海绵吸附miR-375诱导鼻咽癌肿瘤转移和上皮-间质转化。

Long noncoding RNA ROR1-AS1 induces tumor metastasis and epithelial-mesenchymal transition by sponging miR-375 in nasopharyngeal carcinoma.

作者信息

Hou J, Yan J, Ren X-Y, Zhu K, Du X-Y, Li J-J, Xu M

机构信息

Department of Otolaryngology, The Second Affiliated Hospital of Xi'an Jiaotong University, Xian, China.

出版信息

Eur Rev Med Pharmacol Sci. 2020 Jan;24(1):174-180. doi: 10.26355/eurrev_202001_19909.

Abstract

OBJECTIVE

The vital role of long noncoding RNAs (lncRNAs) in tumor progression has been identified in numerous studies. Nasopharyngeal carcinoma (NPC) is one of the most ordinary malignant tumors. This study aims to explore the role of lncRNA ROR1-AS1 in the metastasis of NPC.

PATIENTS AND METHODS

Real Time-quantitative Polymerase Chain Reaction (RT-qPCR) was utilized to measure ROR1-AS1 expression in 50 NPC tissues. The function assays including wound healing assay and transwell assay were conducted to detect the behavior changes of NPC cells after the knockdown of ROR1-AS1, and the epithelial-mesenchymal transition (EMT) process of NPC metastasis was further measured by performing the Western blot assay in vitro. Besides, the target miRNAs were also explored by luciferase assays and RNA immunoprecipitation assay (RIP).

RESULTS

ROR1-AS1 expression level was significantly higher in NPC samples compared with that in adjacent tissues. The knockdown of ROR1-AS1 reduced cell migration and cell invasion of NPC cells, which was identified to inhibit the EMT process of NPC. Furthermore, it was discovered that miR-375 was upregulated via knockdown of ROR1-AS1 and further mechanism assays showed that ROR1-AS1 acted as a competing endogenous RNA via sponging miR-375 in NPC.

CONCLUSIONS

Our study suggests that ROR1-AS1 could act as a sponge for miR-375 and promote cell migration and invasion by inducing EMT process in NPC.

摘要

目的

众多研究已证实长链非编码RNA(lncRNA)在肿瘤进展中发挥着重要作用。鼻咽癌(NPC)是最常见的恶性肿瘤之一。本研究旨在探讨lncRNA ROR1-AS1在鼻咽癌转移中的作用。

患者与方法

采用实时定量聚合酶链反应(RT-qPCR)检测50例鼻咽癌组织中ROR1-AS1的表达。进行包括伤口愈合试验和Transwell试验在内的功能分析,以检测ROR1-AS1敲低后鼻咽癌细胞的行为变化,并通过体外蛋白质免疫印迹法进一步检测鼻咽癌转移的上皮-间质转化(EMT)过程。此外,还通过荧光素酶试验和RNA免疫沉淀试验(RIP)探索了靶标微小RNA(miRNA)。

结果

与癌旁组织相比,鼻咽癌样本中ROR1-AS1表达水平显著更高。ROR1-AS1敲低可降低鼻咽癌细胞的迁移和侵袭能力,这被证实可抑制鼻咽癌的EMT过程。此外,研究发现敲低ROR1-AS1可上调miR-375,进一步的机制分析表明,ROR1-AS1在鼻咽癌中通过海绵吸附miR-375作为竞争性内源RNA发挥作用。

结论

我们的研究表明,ROR1-AS1可作为miR-375的海绵,通过诱导鼻咽癌的EMT过程促进细胞迁移和侵袭。

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