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miR-99a-5p 通过靶向 NOX4 调节人口腔癌细胞的增殖、迁移和侵袭能力。

MiR-99a-5p regulates proliferation, migration and invasion abilities of human oral carcinoma cells by targeting NOX4.

出版信息

Neoplasma. 2017;64(5):666-673. doi: 10.4149/neo_2017_503.

Abstract

Previous research has showed that miR-99a-5p was a tumor suppressor. The aim of our study was to explore the effect of miR-99a-5p on the vitality and proliferation, migration together with the invasion of oral tumor cells via inhibiting the expression of NOX4. QRT-PCR and Western blot were applied to examine the expression level of miR-99a-5p and NOX4 in human oral tumorous and adjacent tissues. Dual luciferase reporter gene assay was applied to confirm that miR-99a-5p negatively regulated directly on NOX4 in TSCC1 cells. Cell transfection and lentiviral vectors were used to up-regulate expression of miR-99a-5p and NOX4, respectively. Cell proliferation, cell cycle, apoptosis and invasion along with the migration in different groups were assessed using MTT assay, colony formation assay, the flow cytometry, transwell assay and the wound healing assay, respectively. MiR-99a-5p was under-expressed in human oral tumor, while NOX4 was over-expressed. There was a negative relationship between miR-99a-5p and NOX4. Up-regulating miR-99a-5p or down-regulating NOX4 suppressed the vitality, proliferation, migration together with invasion of TSCC1 cells. MiR-99a-5p affected the vitality and proliferation, migration together with the invasion of oral tumor cells through targeting NOX4.

摘要

先前的研究表明 miR-99a-5p 是一种肿瘤抑制因子。我们的研究旨在通过抑制 NOX4 的表达,探索 miR-99a-5p 对口腔肿瘤细胞活力、增殖、迁移和侵袭的影响。运用 QRT-PCR 和 Western blot 检测 miR-99a-5p 和 NOX4 在人口腔肿瘤组织及其相邻组织中的表达水平。双荧光素酶报告基因实验证实 miR-99a-5p 可直接负调控 TSCC1 细胞中的 NOX4。通过细胞转染和慢病毒载体分别上调 miR-99a-5p 和 NOX4 的表达。采用 MTT 检测、集落形成实验、流式细胞术、Transwell 检测和划痕愈合实验分别评估不同组细胞的增殖、细胞周期、凋亡和侵袭以及迁移情况。miR-99a-5p 在人口腔肿瘤中低表达,而 NOX4 高表达。miR-99a-5p 与 NOX4 呈负相关。上调 miR-99a-5p 或下调 NOX4 可抑制 TSCC1 细胞的活力、增殖、迁移和侵袭。miR-99a-5p 通过靶向 NOX4 影响口腔肿瘤细胞的活力、增殖、迁移和侵袭。

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