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[微小RNA-99a通过靶向雷帕霉素靶蛋白(mTOR)信号通路抑制口腔鳞状细胞癌的增殖]

[MiR-99a inhibits proliferation of oral squamous cell carcinoma by targeting mTOR pathway].

作者信息

Wang Ke, Peng Guo-Guang, Tan Yu-Lian, He Shan-Zhi, Luo Cui-Fen

机构信息

Stomatological Medical Center of Foshan Traditional Chinese Medicine, Hospital Affiliated to Guangzhou University of Chinese Medicine. Foshan 528000, Guangdong Province, China. E-mail:

出版信息

Shanghai Kou Qiang Yi Xue. 2021 Feb;30(1):44-49.

Abstract

PURPOSE

To investigate miR-99a expression and its effect on proliferation of oral squamous cell carcinoma (OSCC).

METHODS

miRNA microarrays associated with OSCC were identified in GEO database. The expression levels of miR-99a were detected in 63 OSCC tissues and adjacent normal tissues and cell lines. The relationship between clinicopathological parameters and miR-99a expression was analyzed by using ANOVA analysis. The ability of cell growth and clone formation were examined in SCC9 and SCC25 cells transfected with miR-99a mimics. The target genes of miR-99a were predicted by Targetscan software. There resulting data were analyzed using SPSS 19.0 software package.

RESULTS

The differently expressed miRNAs were analyzed based on GSE103931 microarray. miR-99a was significantly downregulated in OSCC tissues and cell lines. miR-99a expression was significantly associated with T stage, pathological grading and patients' prognosis. miR-99a overexpression inhibited OSCC cell proliferation and clone formation, while miR-99a inhibition contributed to decreased proliferation and clone formation ability. In addition, miR-99a combined with mTOR gene's 3'UTR was negatively correlated with mTOR expression in OSCC tissues.

CONCLUSIONS

miR-99a functions as a tumor suppressor in OSCC and inhibits OSCC cell proliferation by targeting mTOR.

摘要

目的

研究miR-99a的表达及其对口腔鳞状细胞癌(OSCC)增殖的影响。

方法

在GEO数据库中鉴定与OSCC相关的miRNA微阵列。检测63例OSCC组织、癌旁正常组织及细胞系中miR-99a的表达水平。采用方差分析分析临床病理参数与miR-99a表达的关系。用miR-99a模拟物转染SCC9和SCC25细胞,检测细胞生长和克隆形成能力。用Targetscan软件预测miR-99a的靶基因。所得数据采用SPSS 19.0软件包进行分析。

结果

基于GSE103931微阵列分析差异表达的miRNA。miR-99a在OSCC组织和细胞系中显著下调。miR-99a表达与T分期、病理分级及患者预后显著相关。miR-99a过表达抑制OSCC细胞增殖和克隆形成,而抑制miR-99a则导致增殖和克隆形成能力下降。此外,miR-99a与mTOR基因的3'UTR结合与OSCC组织中mTOR表达呈负相关。

结论

miR-99a在OSCC中起抑癌作用,通过靶向mTOR抑制OSCC细胞增殖。

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