Department of Medical Oncology, The First Affiliated Hospital of Anhui Medical University, Hefei, China.
Eur Rev Med Pharmacol Sci. 2019 Jul;23(14):6179-6185. doi: 10.26355/eurrev_201907_18431.
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.
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.
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.
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.
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。
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。
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。
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。