Revista: | Brazilian Journal of Pharmaceutical Sciences |
Base de datos: | PERIÓDICA |
Número de sistema: | 000451429 |
ISSN: | 1984-8250 |
Autors: | Shariatnasery, Maria1 Irani, Shiva1 Soleimani, Masoud2 Goodarzi, Navid3 Dinarvand, Rassoul3 |
Institucions: | 1Islamic Azad University, Science and Research Branch, Teherán. Irán 2Tarbiat Modares University, School of Medical Sciences, Teherán. Irán 3Tehran University of Medical Sciences, Faculty of Pharmacy , Teherán. Irán |
Any: | 2020 |
Volum: | 56 |
País: | Brasil |
Idioma: | Inglés |
Tipo de documento: | Artículo |
Enfoque: | Experimental, aplicado |
Resumen en inglés | The functional significance of upregulation miR-34a in combination with albumin-bound paclitaxel nanoparticles in U251 glioblastoma cell line has been evaluated. The MTT assay determined that miR-34a and albumin-bound paclitaxel nanoparticles can reduce cell viability, but the combination of both factors has a stronger effect on cell viability. The application of qRT-PCR has demonstrated that the transduction of miR-34a could lead to exogenous upregulation of miR-34a level and downregulation of SURVIVIN. Moreover, treatment of U251 cells with miR-34a and nanoparticles together considerably inhibit SURVIVIN expression compared to miR-34a and nanoparticles alone. Flow cytometry showed that upon miR-34a overexpression cell cycle arrested in G1 phase, while treatment with nanoparticles increased the cell population in G2 phase. Upregulation of miR-34a along with treatment with nanoparticles elevated the number of cells arrested in G1/ G2 phases of the cell cycle. Expression of miR-34a with albumin-bound paclitaxel nanoparticles reduced cell viability, downregulated SURVIVIN and enhanced cell cycle arrest in G1/G2 phases. Thus, the upregulation of miR-34a with these nanoparticles are potential candidates therapeutic for glioblastoma cancer |
Disciplines | Química, Medicina |
Paraules clau: | Oncología, Farmacología, Nanopartículas, Albúmina, MicroARNs, Paclitaxel, Sinergismo, Proliferación celular, Glioblastoma, Terapia combinada |
Keyword: | Oncology, Pharmacology, Nanoparticles, Albumin, MicroRNAs, Paclitaxel, Synergism, Cell proliferation, Glioblastoma, Combined therapy |
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