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miR612 与食管鳞状细胞癌的发展和转移有关,是通过 TP53 介导的。

miR612 is associated with esophageal squamous cell carcinoma development and metastasis, mediated through TP53.

机构信息

Department of Pathology, Qianfoshan Hospital Affiliated with Shandong University, Jinan, Shandong 250014, P.R. China.

Department of Pathology, Shandong University School of Medicine, Jinan, Shandong 250014, P.R. China.

出版信息

Mol Med Rep. 2017 Aug;16(2):1855-1863. doi: 10.3892/mmr.2017.6808. Epub 2017 Jun 20.

Abstract

MicroRNAs (miRNAs) serve an important role in the regulation of gene expression. In the present study, differential expressions of miRNAs were compared between esophageal squamous cell carcinoma (ESCC) tissues and normal esophageal tissues. In combination with miRNA target prediction databases, a significantly increased expression of miR‑612 was discovered in ESCC. The relationship between miR‑612 and TP53 gene expression and their roles in ESCC invasion and metastasis was further studied by reverse transcription‑quantitative polymerase chain reaction and western blotting in EC109 cells and cancer tissues. The EC109 cell invasion and migration were significantly reduced after miR‑612 expression was inhibited. The levels of wild type TP53 protein and mRNA were lower in ESCC tissues compared to the normal esophageal epithelium. In addition, the mRNA and protein expression levels were reported as downregulated further in tumors with metastasis than in tumors without. In conclusion, miR‑612 is identified as associated with ESCC development and metastasis, likely through the regulation of TP53 expression, which could be a potential therapeutic target.

摘要

微小 RNA(miRNA)在基因表达调控中发挥着重要作用。本研究比较了食管鳞状细胞癌(ESCC)组织与正常食管组织中 miRNA 的差异表达。结合 miRNA 靶基因预测数据库,发现 miR-612 在 ESCC 中表达显著增加。通过逆转录-定量聚合酶链反应和 Western blot 在 EC109 细胞和癌组织中进一步研究了 miR-612 与 TP53 基因表达的关系及其在 ESCC 侵袭和转移中的作用。抑制 miR-612 表达后,EC109 细胞的侵袭和迁移能力显著降低。与正常食管上皮相比,ESCC 组织中野生型 TP53 蛋白和 mRNA 水平较低。此外,报告称转移瘤中的 mRNA 和蛋白表达水平进一步下调。综上所述,miR-612 与 ESCC 的发生和转移有关,可能通过调节 TP53 的表达,这可能成为一种潜在的治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a455/5562086/2b7c32ccc5f3/MMR-16-02-1855-g00.jpg

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