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长链非编码 RNA MNX1-AS1 通过上调 IGF2 促进食管鳞癌细胞的迁移和侵袭。

Long non-coding RNA MNX1-AS1 promotes migration and invasion of esophageal squamous cell carcinoma by upregulating IGF2.

机构信息

Department of Medical Oncology, The First Affiliated Hospital of Anhui Medical University, Hefei, China.

出版信息

Eur Rev Med Pharmacol Sci. 2019 Jul;23(14):6179-6185. doi: 10.26355/eurrev_201907_18431.

Abstract

OBJECTIVE

Esophageal squamous cell carcinoma (ESCC) is a common malignant tumor with a high mortality rate and poor prognosis. In this research, we investigated the exact role of long non-coding ribonucleic acids (lncRNA) MNX1-AS1 in the metastasis of ESCC and its possible mechanism.

PATIENTS AND METHODS

To investigate the functions of MNX1-AS1 in ESCC, quantitative Real Time-Polymerase Chain Reaction (qRT-PCR) was utilized to detect MNX1-AS1 expression of ESCC tissues and cells. Besides, functional assays, including transwell assay and wound healing assay, were performed. Furthermore, qRT-PCR and Western blot assay were used to explore the possible underlying regulatory mechanism.

RESULTS

The expression level of MNX1-AS1 was significantly increased in both ESCC tissues sample and cells. Moreover, knockdown of MNX1-AS1 markedly inhibited the migration and invasion of ESCC cells. Besides, knockdown of MNX1-AS1 remarkably down-regulated the mRNA and protein levels of insulin-like growth factor 2 (IGF2). Furthermore, IGF2 expression was positively correlated with MNX1-AS1 expression in ESCC tissues.

CONCLUSIONS

MNX1-AS1 serves as a potential oncogene in ESCC, which can significantly promote ESCC cell migration and invasion by up-regulating IGF2. Our findings may provide a new therapeutic target of ESCC.

摘要

目的

食管鳞状细胞癌(ESCC)是一种常见的恶性肿瘤,死亡率和预后均较差。本研究旨在探讨长链非编码 RNA(lncRNA)MNX1-AS1 在 ESCC 转移中的确切作用及其可能的机制。

患者与方法

为了研究 MNX1-AS1 在 ESCC 中的功能,我们采用实时定量聚合酶链反应(qRT-PCR)检测 ESCC 组织和细胞中 MNX1-AS1 的表达。此外,还进行了功能测定,包括 Transwell 测定和划痕愈合测定。进一步采用 qRT-PCR 和 Western blot 测定来探讨可能的潜在调控机制。

结果

MNX1-AS1 在 ESCC 组织样本和细胞中的表达水平均显著升高。此外,敲低 MNX1-AS1 可显著抑制 ESCC 细胞的迁移和侵袭。此外,敲低 MNX1-AS1 可显著下调胰岛素样生长因子 2(IGF2)的 mRNA 和蛋白水平。此外,IGF2 的表达与 ESCC 组织中的 MNX1-AS1 表达呈正相关。

结论

MNX1-AS1 是 ESCC 中的一种潜在癌基因,可通过上调 IGF2 显著促进 ESCC 细胞的迁移和侵袭。我们的研究结果可能为 ESCC 提供新的治疗靶点。

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