Upregulation of miR-494 Inhibits Cell Growth and Invasion and Induces Cell Apoptosis by Targeting Cleft Lip and Palate Transmembrane 1-Like in Esophageal Squamous Cell Carcinoma

Background Potential target genes of microRNA (miR)-494 have been reported in many types of cancers. However, the role of miR-494 in esophageal squamous cell carcinoma (ESCC) remains unknown. Aim This study focused on the expression and biological function of miR-494 in ESCC. Methods Using bioinform...

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Veröffentlicht in:Digestive diseases and sciences 2015-05, Vol.60 (5), p.1247-1255
Hauptverfasser: Zhang, Ren, Chen, Xiaonan, Zhang, Shengjie, Zhang, Xueyan, Li, Tong, Liu, Zhicai, Wang, Jinwu, Zang, Wenqiao, Wang, Yuanyuan, Du, Yuwen, Zhao, Guoqiang
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Sprache:eng
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Zusammenfassung:Background Potential target genes of microRNA (miR)-494 have been reported in many types of cancers. However, the role of miR-494 in esophageal squamous cell carcinoma (ESCC) remains unknown. Aim This study focused on the expression and biological function of miR-494 in ESCC. Methods Using bioinformatics analyses, we found that cleft lip and palate transmembrane 1-like (CLPTM1L) was a potential target of miR-494. We performed quantitative real-time (qRT) PCR assays in 37 ESCC tumor tissues to determine the expression of miR-494 and CLPTM1L mRNA, and we analyzed the correlation between both of these factors and clinical characteristics. The cell counting kit-8 and colony formation assays were used to evaluate the effects of miR-494 expression on the proliferation of ESCC cells. The transwell migration assay and flow cytometric apoptosis assay were performed to study the influence of miR-494 on the invasion and apoptosis of ESCC cells. Western blotting, luciferase assays, and CLPTM1L knockdown experiments were used to determine whether CLPTM1L was a target of miR-494. Results The qRT-PCR assays showed significant downregulation of miR-494 ( P  
ISSN:0163-2116
1573-2568
DOI:10.1007/s10620-014-3433-7