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MDM2/p53通路对多发性骨髓瘤RPMI 8226细胞凋亡的调控

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成果类型:
期刊论文
论文标题(英文):
The role of MDM2/p53pathway in regulating apoptosis of multiple myeloma RPMI8226cells
作者:
梁昊;廖灿;李红;刘文龙
通讯作者:
Li, H.
作者机构:
[梁昊] Institute of TCM Diagnostics, Hunan University of Chinese Medicine, Changsha, 410208, China
[廖灿] School of Chinese Medicine, Hunan University of Chinese Medicine, Changsha, 410208, China
[李红] Science and Technology Innovation Center, Hunan University of Chinese Medicine, Changsha, 410208, China
[刘文龙] School of Pharmacy, Hunan University of Chinese Medicine, Changsha, 410208, China
通讯机构:
Science and Technology Innovation Center, Hunan University of Chinese Medicine, Changsha, China
语种:
中文
关键词:
多发性骨髓;凋亡
关键词(英文):
nutlin 3;protein bcl 2;protein MDM2;protein p53;apoptosis;apoptosis rate;Article;cell proliferation;controlled study;flow cytometry;in vitro study;multiple myeloma cell line;protein degradation;protein expression;regulatory mechanism;RPMI-8226/LR-5 cell line;transactivation;Western blotting
期刊:
西安交通大学学报(医学版)
ISSN:
1671-8259
年:
2020
卷:
41
期:
2
页码:
197-200
基金类别:
Supported by the Open Fund of Key Laboratory of Ministry of Education of the People's Republic of China (No.ZYNK201607), Project of Research-oriented Learning and Innovative Experiment for College Students (No.2018-01), National Natural Science Foundation of China (No.81874344), China Postdoctoral Fund Project (No.2018M640755), and Natural the Science Foundation of Hunan Province (No.2019JJ0307)
机构署名:
本校为第一且通讯机构
院系归属:
医学院
中医学院
药学院
中医诊断研究所
摘要:
目的 研究MDM2/p53通路对多发性骨髓瘤(MM)细胞凋亡的调控作用及机制.方法 体外培养人MM细胞株(RPMI 8226)并分为实验组(Nutlin-3a)和对照组(药物溶剂),采用CCK-8法检测各组细胞的增殖情况和抑制率,Western blot检测凋亡相关蛋白表达,流式细胞术检测细胞凋亡情况.结果 与对照组相比,24、48、72 h时间点实验组细胞增殖明显降低,抑制率明显增高(P
摘要(英文):
Objective:To study the regulatory effect and mechanism of MDM2/p53 pathway on apoptosis in multiple myeloma (MM). Methods: RPMI8226 cells were cultured in vitro and divided into Nutlin-3a group, control group and blank group. CCK-8 method was used to detect the cell inhibition rate, Western blot was used to detect the expression of apoptosis-related protein, and flow cytometry was used to detect the apoptosis in the two groups. Results: Compared with that in control group, the inhibition rate of cells in the experimental group increased signifi...

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