miR-137 Regulates Proliferation, Migration, Invasion and EMT of Nasopharyngeal Carcinoma Cells by Targeting TWIST1

被引:2
|
作者
Fan, Kaimei [1 ]
Zhu, Huicheng [2 ]
Qi, Lingqiang [3 ]
Huang, Yingliang [1 ]
Xia, Xiaoping [1 ]
Wu, Kai [1 ]
机构
[1] First Peoples Hosp Linping Dist, Dept Otorhinolaryngol, Hangzhou 310000, Peoples R China
[2] LinPing Hosp Integrated Tradit Chinese & Western, Dept Otorhinolaryngol, Hangzhou 310000, Peoples R China
[3] Hangzhou Normal Univ, Affiliated Xiaoshan Hosp, Dept Otorhinolaryngol, Hangzhou 310000, Peoples R China
关键词
miR-137; Nasopharyngeal Carcinoma (NPC); Twist Family BHLH Transcription Factor 1 (TWIST1); Epithelial-Mesenchymal Transition (EMT); EPITHELIAL-MESENCHYMAL TRANSITION; MOLECULAR-MECHANISMS; BREAST-CANCER; METASTASIS; MICRORNAS; EXPRESSION; PHENOTYPE; CADHERIN;
D O I
10.1166/sam.2023.4439
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
To investigate the effects of miR-137 on biological cell function of nasopharyngeal carcinoma (NPC) cells. Totally, 31 pairs of NPC tissues and para-cancer tissues were collected. Meanwhile, human immortalized nasopharyngeal epithelial cell lines (NP69) and human NPC cell lines (6-10B) were cultured. The abilities of cell proliferation, invasion and migration were detected by CCK-8 and Transwell assay, respectively. The relative protein and mRNA expression level was detected by Western blot and quantitative real-time polymerase chain reaction (qRT-PCR) analysis. In quantitative real-time polymerase chain reaction (qRT-PCR) experiment, miR-137 was found widely low-expressed in clinical samples and cell lines of nasopharyngeal carcinoma (NPC). On-line target gene prediction software was applied to screen potential downstream target of miR-137 in NPC. Then, Twist Family BHLH Transcription Factor 1 (TWIST1) was verified by luciferase reporter assay and Western IP: 203.8.109.20 On: Thu, 11 May 2023 08:15:12 blot experiments as a target for negative regulation of miR-137 in NPC cells. We up-regulated the expression of Copyright: American Scientific Publishers miR-137 and/or TWIST1 in 6-10B in vitro, and then examined the effects of cell function after by CCK8, Tran-Delivered by Ingenta swell, scratch-wound and Western blot experiments. The results showed that decreased expression of TWIST1 resulting from up-regulation of miR-137 in 6-10B cells could inhibit the biological functions of cells including proliferation, invasion, migration and process of epithelial-mesenchymal transition (EMT). Our research discov-ered the suppressor function of miR-137 on NPC cells by targeting TWIST1, suggesting that miR-137 could be used as a potential therapeutic target for NPC.
引用
收藏
页码:361 / 368
页数:8
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