首页 | 本学科首页   官方微博 | 高级检索  
     

姜黄素对K562细胞STAT5信号分子的影响
引用本文:陈伟红,陈燕,谷俊侠,何静. 姜黄素对K562细胞STAT5信号分子的影响[J]. 中华血液学杂志, 2004, 25(3): 151-153
作者姓名:陈伟红  陈燕  谷俊侠  何静
作者单位:430022,武汉,华中科技大学同济医学院附属协和医院血液科
基金项目:国家自然科学基金资助项目 (3 0 2 71672 )
摘    要:目的 了解姜黄素对信号分子的影响 ,探讨其抗白血病的分子机制。方法 用MTT比色法检测细胞增殖活性。用原位杂交法检测细胞STAT5mRNA的表达。用免疫印迹法 (Westernblot ting)检测细胞STAT5蛋白的表达。结果 ①姜黄素抑制K5 6 2细胞增殖与作用时间及姜黄素浓度分别呈依赖关系 ,最适作用时间为 12h ,最适作用浓度为 2 5 μmol L。②姜黄素组K5 6 2细胞STAT5mRNA表达的阳性率为 19% ,与K5 6 2细胞组 (31% )相比明显减少 (P <0 .0 1)。③姜黄素组K5 6 2细胞STAT5蛋白的表达 (A值为 15 2 6 6± 76 9)与K5 6 2细胞组 (A值为 2 5 781± 12 4 0 )相比明显减低 (P <0 .0 1)。结论 姜黄素能抑制K5 6 2细胞STAT5信号分子的活化及表达 ,进一步抑制白血病细胞的增殖。

关 键 词:姜黄素  细胞系  K562  分子信号  STAT5
修稿时间:2003-04-07

Effect of curcumin on STAT5 signaling molecule in K562 cells
CHEN Wei-hong,CHEN Yan,GU Jun-xia,HE Jing. Effect of curcumin on STAT5 signaling molecule in K562 cells[J]. Chinese Journal of Hematology, 2004, 25(3): 151-153
Authors:CHEN Wei-hong  CHEN Yan  GU Jun-xia  HE Jing
Affiliation:Department of Hematology, Affiliated Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430022, China.
Abstract:OBJECTIVE: To investigate the effect of curcumin on STAT 5 signaling molecule in K562 cells and its molecular mechanism of antileukemia. METHODS: Cell proliferation was studied by tetrazolium dye assay. The expressions of STAT5 mRNA and protein were assayed by in situ hybridization, and Western blotting respectively. RESULTS: Curcumin could inhibit K562 cell proliferation in a time- and dose-dependent manner. The percentage of STAT5-positive cells was 19% in curcunin group, significantly less than 31% of that in K562 cell group (P < 0.01). The A value of the expression level of STAT5 protein in curcumin group was 15 266 +/- 769, significantly less than 25 781 +/- 1240 of that in K562 cell group (P < 0.01). CONCLUSION: The expressions of STAT5 mRNA and protein in K562 cells were inhibited by curcumin and curcumin could inhibit K562 cell proliferation.
Keywords:Curcumin  Cell line  K562  Signaling molecule  STAT5
本文献已被 CNKI 万方数据 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号