RETRACTED: MicroRNA-338-3p suppresses tumor growth of esophageal squamous cell carcinoma in vitro and in vivo (Retracted article. See vol. 24, 2021)

被引:12
|
作者
Li, Xinyu [1 ]
Li, Zhihong [2 ]
Yang, Guiyun [1 ]
Pan, Zhenxiang [1 ]
机构
[1] Jilin Univ, Hosp 2, Dept Anesthesiol, Changchun 130041, Jilin, Peoples R China
[2] Jilin Univ, Hosp 1, Dept Thorac Surg, Changchun 130021, Jilin, Peoples R China
关键词
esophageal squamous cell carcinoma; microRNAs; microRNA-338-3p; tumor growth; COLORECTAL-CARCINOMA; INVASION; CANCER; PROLIFERATION; PROGRESS; EXPRESSION; SIGNATURES; MIGRATION; BARRIERS;
D O I
10.3892/mmr.2015.3820
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Accumulating evidence has shown that microRNAs (miRNAs) are aberrantly expressed in human esophageal squamous cell carcinoma (ESCC) and are crucial in tumorigenesis, among which miR-338-3p has been examined to be downregulated in patients with ESCC. However, the role of ffiiR-338-3p in ESCC remains to be elucidated. In the present study, the role of riiiR:338-3p on the growth and survival of an ESCC cell line was determined with several in vitro approaches and in nude fliouse models. It was determined that miR-338-3p expression was frequently downregulated in ESCC tissue compared with corresponding adjacent non-tumor tissue, and that its expression was significantly correlated with tumor stage and metastasis. Overexpression of miR-338-3p in ESCC cells suppressed cell proliferation, colony formation, migration and invasion, and induced cell arrest at the GO/G1 stage and cell apoptosis in vitro. In addition, it was demonstrated that overexpression of miR-338-3p significantly suppresses tumor growth of xenograft tumors in mice (P<0.05). These findings revealed that miR-338-3p may act as a tumor suppressor in ESCC, and its dysregulation may be involved in the initiation and development of human ESCC. In addition, it was suggested that miR-338-3p may be a potential therapeutic agent for treatment of ESCC.
引用
收藏
页码:3951 / 3957
页数:7
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