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miR-139-5p 通过靶向 HOXA9 抑制口腔鳞状细胞癌细胞的肿瘤发生和进展。

MiR-139-5p inhibits the tumorigenesis and progression of oral squamous carcinoma cells by targeting HOXA9.

机构信息

Department of Plastic Surgery, Henan Provincial People's Hospital, Zhengzhou, Henan, China.

出版信息

J Cell Mol Med. 2017 Dec;21(12):3730-3740. doi: 10.1111/jcmm.13282. Epub 2017 Aug 5.

Abstract

Our study sought to clarify the effects of microRNA-139-5p (miR-139-5p) in the tumorigenesis and progression of oral squamous cell carcinoma (OSCC) by regulating HOXA9. MiR-139-5p and HOXA9 expression in OSCC tissues, tumour adjacent tissues, OSCC cells and normal cells were tested by qRT-PCR. SAS and CAL-27 cell lines were selected in among four OSCC cell lines and then transfected with miR-139-5p mimics, pEGFP-HOXA9 and cotransfected with miR-139-5p mimics + pEGFP-HOXA9. We used MTT, colony formation, transwell and wound healing assays to analyse cell viability, proliferation, invasion and migration. The target relationship between miR-139-5p and HOXA9 was verified by luciferase reporter assay and Western blot, respectively. MiR-139-5p was down-regulated, whereas HOXA9 was up-regulated in OSCC tissues and cells. The proliferation, invasion and migration ability of SAS and CAL-27 cells in miR-139-5p mimics group were significantly weaker than those in the control group and the miR-NC group (P < 0.01). MiR-139-5p can negatively regulate HOXA9. The proliferation, invasion and migration of SAS and CAL-27 cells in the miR-139-5p mimics + pEGFP-HOXA9 group were not significantly different from those in the blank control and negative control groups (P > 0.05). Our results indicated that miR-139-5p could directly inhibit HOXA9, which might be a potential mechanism in inhibiting the proliferation, invasiveness and migration of OSCC cells.

摘要

我们的研究旨在通过调节 HOXA9 来阐明 microRNA-139-5p(miR-139-5p)在口腔鳞状细胞癌(OSCC)发生和进展中的作用。通过 qRT-PCR 检测 OSCC 组织、肿瘤旁组织、OSCC 细胞和正常细胞中的 miR-139-5p 和 HOXA9 的表达。在四个 OSCC 细胞系中选择 SAS 和 CAL-27 细胞系,然后用 miR-139-5p 模拟物、pEGFP-HOXA9 转染,并用 miR-139-5p 模拟物+ pEGFP-HOXA9 共转染。我们使用 MTT、集落形成、transwell 和划痕愈合实验来分析细胞活力、增殖、侵袭和迁移。通过荧光素酶报告基因测定和 Western blot 分别验证 miR-139-5p 和 HOXA9 之间的靶关系。miR-139-5p 在 OSCC 组织和细胞中下调,而 HOXA9 上调。miR-139-5p 模拟物组 SAS 和 CAL-27 细胞的增殖、侵袭和迁移能力明显弱于对照组和 miR-NC 组(P<0.01)。miR-139-5p 可以负调控 HOXA9。miR-139-5p 模拟物+ pEGFP-HOXA9 组 SAS 和 CAL-27 细胞的增殖、侵袭和迁移能力与空白对照组和阴性对照组无显著差异(P>0.05)。我们的结果表明,miR-139-5p 可以直接抑制 HOXA9,这可能是抑制 OSCC 细胞增殖、侵袭和迁移的潜在机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5a8/5706525/0b3d63d87cf3/JCMM-21-3730-g001.jpg

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