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miR-497 inhibited proliferation, migration and invasion of thyroid papillary carcinoma cells by negatively regulating YAP1 expression

PURPOSE: This article aimed to investigate the effect of miR-497 on thyroid papillary carcinoma. MATERIALS AND METHODS: miR-497 expression was analyzed using The Cancer Genome Atlas. A total of 56 papillary thyroid carcinoma patients’ tumor tissues and normal tissues were collected. Nthy-ori 3-1 and...

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Detalles Bibliográficos
Autores principales: Cheng, Hui, Dong, Hui, Feng, Jianlin, Tian, Hongyan, Zhang, Haixia, Xu, Lina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6091470/
https://www.ncbi.nlm.nih.gov/pubmed/30127619
http://dx.doi.org/10.2147/OTT.S164052
Descripción
Sumario:PURPOSE: This article aimed to investigate the effect of miR-497 on thyroid papillary carcinoma. MATERIALS AND METHODS: miR-497 expression was analyzed using The Cancer Genome Atlas. A total of 56 papillary thyroid carcinoma patients’ tumor tissues and normal tissues were collected. Nthy-ori 3-1 and K1 cells were cultured. K1 cells were also transfected. Quantitative real-time polymerase chain reaction and Western blot were used to detect miR-497 and yes-associated protein 1 (YAP1) expression. Luciferase reporter assay was performed. MTT and Transwell assay were conducted to measure cells’ proliferation, migration and invasion. Immunofluorescence detection was used to detect YAP1-positive cells. RESULTS: miR-497 was downregulated, while YAP1 was upregulated in thyroid papillary carcinoma tissues and K1 cells (P<0.05). Compared with the negative control group, the OD495 value and the migrating and invasive cell number were significantly lower in miR-497 mimics group and significantly higher in miR-497 inhibitor group (P<0.05). YAP1 was the target gene of miR-497. Compared with blank group, the OD495 value and the migrating and invasive cell number were significantly lower in si-YAP1 group and significantly higher in miR-497 inhibitor group (P<0.05), while no significant difference was found between si-YAP1+inhibitors group and blank group in these indicators. CONCLUSION: miR-497 regulated the proliferation, migration and invasion of K1 cells by negatively regulating YAP1 expression.