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MiR-139-5p Inhibits the Development of Gastric Cancer through Targeting TPD52

BACKGROUND: Many researchers have confirmed that miRNAs are involved in the pathogenesis of gastric cancer (GC). This study focused on investigating the specific functions of miR-139-5p in GC. METHODS: MiR-139-5p and TPD52 expressions were observed by qRT-PCR or western blot in GC. The functional me...

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Detalles Bibliográficos
Autores principales: Li, Yuanbo, Sun, Yan, Li, Zhenlu, Li, Shikuan, Wu, Changliang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8866006/
https://www.ncbi.nlm.nih.gov/pubmed/35222884
http://dx.doi.org/10.1155/2022/4033373
Descripción
Sumario:BACKGROUND: Many researchers have confirmed that miRNAs are involved in the pathogenesis of gastric cancer (GC). This study focused on investigating the specific functions of miR-139-5p in GC. METHODS: MiR-139-5p and TPD52 expressions were observed by qRT-PCR or western blot in GC. The functional mechanism of miR-139-5p was explored by the luciferase reporter assay, transwell assay, and MTT assay. RESULTS: MiR-139-5p downregulation and TPD52 upregulation were detected in GC. Adverse clinical features and prognosis in GC patients were related to low miR-139-5p expression. MiR-139-5p overexpression restrained GC cell proliferation and metastasis. Furthermore, miR-139-5p directly targeted TPD52. TPD52 silencing blocked GC progression. And TPD52 upregulation weakened the antitumor effect of miR-139-5p in GC. CONCLUSION: MiR-139-5p inhibits GC cell proliferation and metastasis through downregulating TPD52.