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白花丹素对骨肉瘤细胞系U2OS的作用及其机制
引用本文:田林强,陈安民,尹德龙,宫晨,任晔,郭风劲. 白花丹素对骨肉瘤细胞系U2OS的作用及其机制[J]. 肿瘤防治研究, 2012, 39(11): 1285-1288. DOI: 10.3971/j.issn.1000-8578.2012.11.001
作者姓名:田林强  陈安民  尹德龙  宫晨  任晔  郭风劲
作者单位:430030武汉,华中科技大学同济医学院附属同济医院骨科
基金项目:973课题资助项目(2002CB513100)
摘    要:目的研究白花丹素对骨肉瘤细胞系U2OS的作用,并初步探讨其作用机制。方法用CCK-8法检测白花丹素对骨肉瘤细胞的促凋亡作用;用HOECHST 33342染色研究白花丹素对骨肉瘤细胞作用后的形态学变化;用Western blot法检测白花丹素作用后骨肉瘤细胞MDM2和p53蛋白表达情况。结果CCK-8结果显示白花丹素对骨肉瘤细胞有明显的抑制作用,而且呈浓度依赖性;HOECHST 33342染色结果显示白花丹素对骨肉瘤U2OS 细胞的抑制作用主要是通过促进凋亡来实现;Western blot结果显示白花丹素能够改变p53/MDM2基因表达比例。结论白花丹素通过细胞凋亡途径抑制骨肉瘤细胞系U2OS细胞的生长。

关 键 词:白花丹素  骨肉瘤细胞  凋亡  p53基因  MDM2基因  
收稿时间:2011-12-08;

Effect and Mechanism of Plumbagin in Human Osteosarcoma Cell Line U2OS
Tian Linqiang,Chen Anmin,Yin Delong,Gong Chen,Ren Ye,Guo Fengjin. Effect and Mechanism of Plumbagin in Human Osteosarcoma Cell Line U2OS[J]. Cancer Research on Prevention and Treatment, 2012, 39(11): 1285-1288. DOI: 10.3971/j.issn.1000-8578.2012.11.001
Authors:Tian Linqiang  Chen Anmin  Yin Delong  Gong Chen  Ren Ye  Guo Fengjin
Affiliation:Department of Orthopedics,Tongji Hospital,Tongji Medical College,Huazhong University of Science and Technology,Wuhan 430030,China
Abstract:Objective
To explore the effect of plumbagin on the growth of osteosarcoma cell line U2OS and its possible underlying mechanisms.MethodsCell apoptosis of plumbagin against osteosarcoma was studied by CCK-8 assay;morphological changes was studied by HOECHST 33342 staining;the expression of p53 and MDM2 gene was studied by Western blot assay.ResultsCCK-8 assay showed that plumbagin had an obvious inhibition on osteosarcoma cell line in a dose-dependent manner;HOECHST 33342 staining showed that plumbagin inhibited the growth of osteosarcoma cell line U2OS through the promotion of apoptosis;Western blot assay showed that plumbagin played the role by changing the expression proportion of p53 and MDM2.ConclusionPlumbagin inhibited osteosarcoma cell line U2OS cells growth through cell apoptotic pathways.
Keywords:Plumbagin  Osteosarcoma cells  Apoptosis  p53 gene  MDM2 gene
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