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长链非编码 RNA ROR1-AS1 通过靶向 miR-375 增强结直肠癌转移。

Long non-coding RNA ROR1-AS1 enhances colorectal cancer metastasis by targeting miR-375.

机构信息

Department of Emergency, Tianjin Union Medical Center, Tianjin, China.

出版信息

Eur Rev Med Pharmacol Sci. 2019 Aug;23(16):6899-6905. doi: 10.26355/eurrev_201908_18729.

Abstract

OBJECTIVE

Recent research has proved that long non-coding RNAs (lncRNAs) play an important role in tumorigenesis. In this research, lncRNA ROR1-AS1 was explored to identify its role in the development of colorectal cancer (CRC).

PATIENTS AND METHODS

Real Time-quantitative Polymerase Chain Reaction (RT-qPCR) was utilized to measure ROR1-AS1 expression of CRC tissues. Besides, function assays including wound healing assay and transwell assay were conducted to detect the effect of ROR1-AS1 on the metastasis of CRC. Furthermore, Luciferase assays and RNA immunoprecipitation assay (RIP) were used to explore the underlying mechanism.

RESULTS

By comparison with ROR1-AS1 expression in adjacent tissues, the ROR1-AS1 expression level was significantly higher in CRC samples. Moreover, loss of ROR1-AS1 inhibited cell migration and cell invasion of CRC cells. Besides, gain of ROR1-AS1 enhanced cell migration and cell invasion of CRC cells. Furthermore, it was found that ROR1-AS1 acted as a competing endogenous RNA via sponging miR-375 in CRC.

CONCLUSIONS

The present study suggests that ROR1-AS1 could promote cell migration and invasion of CRC by sponging miR-375, which may offer a potential therapeutic target in CRC.

摘要

目的

最近的研究证明,长非编码 RNA(lncRNA)在肿瘤发生中起着重要作用。在这项研究中,探索了 lncRNA ROR1-AS1,以确定其在结直肠癌(CRC)发展中的作用。

患者和方法

实时定量聚合酶链反应(RT-qPCR)用于测量 CRC 组织中 ROR1-AS1 的表达。此外,还进行了功能测定,包括划痕愈合测定和 Transwell 测定,以检测 ROR1-AS1 对 CRC 转移的影响。此外,还使用荧光素酶测定和 RNA 免疫沉淀测定(RIP)来探讨潜在的机制。

结果

与相邻组织中 ROR1-AS1 的表达相比,CRC 样本中 ROR1-AS1 的表达水平显著升高。此外,ROR1-AS1 的缺失抑制了 CRC 细胞的迁移和侵袭。此外,ROR1-AS1 的增加增强了 CRC 细胞的迁移和侵袭。此外,研究发现 ROR1-AS1 通过在 CRC 中作为竞争内源性 RNA 来海绵吸附 miR-375。

结论

本研究表明,ROR1-AS1 可通过海绵吸附 miR-375 促进 CRC 细胞的迁移和侵袭,这可能为 CRC 提供一个潜在的治疗靶点。

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