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Effects of Arf6 downregulation on biological characteristics of human prostate cancer cells

OBJECTIVE: To evaluate the effects of Arf6 downregulation on human prostate cancer cells. MATERIALS AND METHODS: The effects of Arf6 downregulation on cell proliferation, migration, invasion and apoptosis were assessed by MTT, BrdU, scratch, Transwell assays and flow cytometry respectively. AKT, p-A...

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Detalles Bibliográficos
Autores principales: Lei, Haiming, Ma, Fujun, Jia, Renfeng, Tan, Bo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade Brasileira de Urologia 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7527080/
https://www.ncbi.nlm.nih.gov/pubmed/32822124
http://dx.doi.org/10.1590/S1677-5538.IBJU.2019.0499
Descripción
Sumario:OBJECTIVE: To evaluate the effects of Arf6 downregulation on human prostate cancer cells. MATERIALS AND METHODS: The effects of Arf6 downregulation on cell proliferation, migration, invasion and apoptosis were assessed by MTT, BrdU, scratch, Transwell assays and flow cytometry respectively. AKT, p-AKT, ERK1/2, p-ERK1/2 and Rac1 protein expressions were detected by Western blot. RESULTS: Downregulating Arf6 by siRNA interference suppressed the mRNA and protein expressions of Arf6. The proliferation capacities of siRNA group at 48h, 72h, and 96h were significantly lower than those of control group (P <0.05). The migration distance of siRNA group at 18h was significantly shorter than that of control group (P <0.01). The number of cells penetrating Transwell chamber membrane significantly decreased in siRNA group compared with that of control group (P <0.01). After 24h, negative control and normal control groups had similar apoptotic rates (P >0.05) which were both significantly lower than that of siRNA group (P <0.01). After Arf6 expression was downregulated, p-ERK1/2 and Rac1 protein expressions were significantly lower than those of control group (P <0.05). CONCLUSION: Downregulating Arf6 expression can inhibit the proliferation, migration and invasion of prostate cancer cells in vitro, which may be related to ERK1/2 phosphorylation and Rac1 downregulation.