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长链非编码 RNA ST8SIA6-AS1 通过调控 miR-5195/PCBP2 轴促进结直肠癌细胞的增殖、迁移和侵袭。

LncRNA ST8SIA6-AS1 promotes colorectal cancer cell proliferation, migration and invasion by regulating the miR-5195/PCBP2 axis.

机构信息

Department of Gastrointestinal Surgery, Suqian First Hospital, Suqian, P.R. China.

出版信息

Eur Rev Med Pharmacol Sci. 2020 Apr;24(8):4203-4211. doi: 10.26355/eurrev_202004_21000.

Abstract

OBJECTIVE

Long non-coding RNAs (lncRNAs) have been reported to play a vital role in the development and progression of various cancers, including colorectal cancer (CRC). Although the dysregulation of lncRNA ST8SIA6-AS1 participates in the development of multiple malignancies, the underlying molecular mechanisms of ST8SIA6-AS1 in regulating CRC progression remain to be fully discovered.

PATIENTS AND METHODS

The expression level of lncRNA ST8SIA6-AS1 was examined in the tumor tissues and paracancerous tissues of CRC patients. Quantitative Real Time-Polymerase Chain Reaction (qRT-PCR) was utilized to examine the expression levels of ST8SIA6-AS1, miR-5195, and Poly-(C) Binding Protein 2 (PCBP2). The protein expression level of PCBP2 was detected by Western blotting. MTT assay was performed to measure the proliferation of HCT-116 and SW480 cells. Cell migration and invasion abilities were measured by transwell assay. Luciferase reporter assay was used to examine the interaction between miR-5195 and ST8SIA6-AS1 or PCBP2.

RESULTS

This study revealed that lncRNA ST8SIA6-AS1 was upregulated in CRC tissues and cells. Knockdown of ST8SIA6-AS1 inhibited proliferation, migration, and invasion of CRC cells. Moreover, ST8SIA6-AS1 was proved to inhibit miR-5195 expression by directly targeting miR-5195. In addition, it was demonstrated that overexpression of miR-5195 inhibited CRC progression. Furthermore, PCBP2 was shown to enhance sh-ST8SIA6-AS1 and miR-5195 mimics-attenuated cell proliferation, migration, and invasion by directly binding to miR-5195.

CONCLUSIONS

Our study revealed that ST8SIA6-AS1 promoted CRC progression via the miR-5195/PCBP2 axis. This study may provide an improved understanding of the pathogenesis of CRC.

摘要

目的

长链非编码 RNA(lncRNA)已被报道在包括结直肠癌(CRC)在内的各种癌症的发生和发展中发挥重要作用。尽管 lncRNA ST8SIA6-AS1 的失调参与了多种恶性肿瘤的发生,但 ST8SIA6-AS1 调节 CRC 进展的潜在分子机制仍有待充分发现。

患者和方法

检测了 CRC 患者肿瘤组织和癌旁组织中 lncRNA ST8SIA6-AS1 的表达水平。采用实时定量聚合酶链反应(qRT-PCR)检测 ST8SIA6-AS1、miR-5195 和多聚(C)结合蛋白 2(PCBP2)的表达水平。采用 Western blot 检测 PCBP2 的蛋白表达水平。采用 MTT 法检测 HCT-116 和 SW480 细胞的增殖能力。通过 Transwell 实验检测细胞迁移和侵袭能力。采用荧光素酶报告基因实验检测 miR-5195 与 ST8SIA6-AS1 或 PCBP2 之间的相互作用。

结果

本研究表明,lncRNA ST8SIA6-AS1 在 CRC 组织和细胞中上调。ST8SIA6-AS1 的敲低抑制了 CRC 细胞的增殖、迁移和侵袭。此外,通过直接靶向 miR-5195,证实 ST8SIA6-AS1 抑制 miR-5195 的表达。此外,研究表明过表达 miR-5195 抑制 CRC 进展。此外,PCBP2 被证明通过直接结合 miR-5195 增强 sh-ST8SIA6-AS1 和 miR-5195 模拟物减弱细胞增殖、迁移和侵袭。

结论

本研究揭示了 ST8SIA6-AS1 通过 miR-5195/PCBP2 轴促进 CRC 进展。本研究可能为 CRC 的发病机制提供了更深入的认识。

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