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慢病毒介导MicroRNA-376b-3p 对垂体腺瘤细胞增殖和凋亡的 影响及机制探究.
- Source :
-
Progress in Modern Biomedicine . 2020, Vol. 20 Issue 22, p4225-4228. 4p. - Publication Year :
- 2020
-
Abstract
- Objective: To investigate the effect of lentivirus-mediated microrna-376b-3p on the proliferation and apoptosis of pituitary adenomas and its possible mechanism. Methods: Taking human pituitary adenoma cell lines cultured in vitro as the research object, the microRNA-376b-3p mimics group (control group) and lenti-sh MicroRNA-376b-3p group (drug group) were established respectively, and the MTT method was used to detect MicroRNA-376b-3p on the proliferation of pituitary adenoma cells, the AnnexinV-FITC/PI double staining method was used to detect the effect of MicroRNA-376b-3p on the apoptosis rate of pituitary adenoma cells, and the Western blot method was used to detect the effect of MicroRNA-376b-3p on HMGA2, Bax, Caspase-3 protein expression. Result: (1) Lentivirus-mediated Microrna-376b-3p could significantly inhibit the proliferation of pituitary adenoma cells (P<0.05). (2) At 12, 24 and 48 h after microrna-376b-3p intervention, the apoptosis rate of pituitary gland cells in the control group was significantly lower than that in the drug group (P<0.05). Conclusions: (3) After transfection with microrna-376b-3p transformation, the expression of Bax protein increased, and the expression of Bcl-2, Caspase-3, Survivin and HMGA2 protein decreased (P<0.05). Lentivirus-mediated Microrna-376b-3p could significantly inhibit the proliferation of pituitary adenoma cells and induce apoptosis. The mechanism of microrna-376b-3p may be related to its targeted down-regulation of HMGA2 expression, up-regulation of Bax protein expression and regulation of survivin protein expression. [ABSTRACT FROM AUTHOR]
Details
- Language :
- Chinese
- ISSN :
- 16736273
- Volume :
- 20
- Issue :
- 22
- Database :
- Academic Search Index
- Journal :
- Progress in Modern Biomedicine
- Publication Type :
- Academic Journal
- Accession number :
- 148027065
- Full Text :
- https://doi.org/10.13241/j.cnki.pmb.2020.22.005