Restoration of miR-143 reduces migration and proliferation of bladder cancer cells by regulating signaling pathways involved in EMT

被引:14
作者
Asghariazar, Vahid [1 ,2 ]
Kadkhodayi, Mahtab [1 ,3 ]
Mansoori, Behzad [4 ]
Mohammadi, Ali [1 ,5 ]
Baradaran, Behzad [1 ]
机构
[1] Tabriz Univ Med Sci, Immunol Res Ctr, Gholghasht Ave, Tabriz, Iran
[2] Tabriz Univ Med Sci, Fac Med, Dept Med Genet, Tabriz, Iran
[3] Univ Tabriz, Fac Nat Sci, Dept Anim Biol, Tabriz, Iran
[4] Wistar Inst Anat & Biol, Cellular & Mol Oncogenesis Program, 3601 Spruce St, Philadelphia, PA 19104 USA
[5] Univ Southern Denmark, Inst Mol Med, Dept Canc & Inflammat Res, Odense, Denmark
关键词
MicroRNA; Apoptosis; Metastasis; Invasion; EJ138; Signaling pathways; EPITHELIAL-MESENCHYMAL TRANSITION; C-MYC; EXPRESSION; APOPTOSIS; CXCR4; PATHOGENESIS; INVASION; GROWTH;
D O I
10.1016/j.mcp.2022.101794
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
MicroRNAs (miRNAs), a class of regulatory endogenous short RNAs, are involved in various biological functions by targeting the mRNA of multiple protein-coding genes and influencing their related signaling pathways. In this investigation, we upregulated microRNA-143 (miR-143) expression levels in bladder cancer (BC) EJ138 cells by pCMV-miR-143 vectors. The efficacy of transfection was verified by Flow cytometry. The influence of miR-143 overexpression on BC cells migration, proliferation, and apoptosis was detected using wound-healing assay, MTT assay, and DAPI and Annexin V/PI staining, respectively. The results demonstrated that upregulation of miR-143 in BC EJ138 cells leads to inhibited proliferation and migration. Also, restoration of miR-143 was negatively associated with the expression levels of metastatic, apoptotic, invasion, and EMT-related genes, including C-Myc, CXCR4, MDM2, Vimentin, Snail-1, and MMP-9, along with increased E-Cadherin and TP53 expression. Therefore, miR-143 may be considered a potential therapeutic target for BC.
引用
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页数:10
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