MiR‐873‐5p modulates progression of tongue squamous cell carcinoma via targeting <i>SEC11A</i>

细胞凋亡 流式细胞术 细胞生长 污渍 细胞迁移 转染 细胞 癌症研究 下调和上调 小RNA 伤口愈合 化学 医学 生物 舌头 免疫组织化学 基因敲除 头颈部鳞状细胞癌 癌变 基底细胞 癌症 转移 细胞培养 分子生物学 免疫学 基因 生物化学 遗传学
作者
Yao Yao,Xiao-Qin Liu,Fengying Yang,Jing-Wen Mu
出处
期刊:Oral Diseases [Wiley]
卷期号:28 (6): 1509-1518 被引量:3
标识
DOI:10.1111/odi.13830
摘要

To explore the effect of miR-873-5p on proliferation, apoptosis, migration, and invasion of tongue squamous cell carcinoma (TSCC) by targeting SEC11A.Tongue squamous cell carcinoma tissues were collected and performed by qRT-PCR and Western blotting to determine the expression of miR-873-5p and SPC18. SCC9 and CAL-27 cells were transfected and divided into Mock, mimic NC, miR-873-5p mimic, SEC11A, and miR-873-5p mimic + SEC11A groups. Then, a series of experiments including cell count kit 8 (CCK-8), wound healing, Transwell, and flow cytometry were conducted. Besides, Western blotting was used to detect the expression of SPC18 and EGFR pathway-related proteins.MiR-873-5p was downregulated while SPC18 was upregulated in TSCC, and miR-873-5p was negatively correlated with SPC18. Dual luciferase reporter gene assay confirmed SEC11A to be a target of miR-873-5p. Cell proliferation, migration, and invasion of SCC9 and CAL-27 cells in miR-873-5p mimic group were decreased with increased cell apoptosis, presenting with downregulations of SPC18 and EGFR pathway-related proteins, while cells in SEC11A group manifested totally different changes. Moreover, the inhibitory effect of miR-873-5p mimic on TSCC cell growth was abolished by SEC11A overexpression.Overexpression of miR-873-5p may suppress cell proliferation, migration, and invasion, but facilitate apoptosis in TSCC via targeting SEC11A.

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