Wu Qing, Chen Yan, Li Xing-Gang, Tang Yuan-Yan
Institute of Hematology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430022, China.
Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2006 Apr;14(2):293-7.
The purpose of this study was to investigate the effect of curcumin on proliferation of B-NHL Raji cell line and explore the relationship between this effect and regulatory expression of p300 and HDAC1 transcription. The in vitro cultured Raji cells were treated with curcumin at various concentrations (6.25-50 micromol/L) and at different time points (0, 6, 12, 24 and 48 hours), the inhibitory ratio of cell growth was measured by MTT assay, the cell apoptosis rate was detected by flow cytometry with Annexin V-FITC/PI double staining, the changes of p300 and HDAC1 mRNA expression and protein level in Raji cells were determined by RT-PCR and Western blot. The results showed that the curcumin could inhibit Raji cell proliferation in significant time-and concentration-dependent manners, IC50 at 24 hours was 25 micromol/L; the curcumin could induce apoptosis of Raji cells in concentration-dependent manner, apoptosis rate was 14.38%-61.18%. The curcumin significantly inhibited activity and expression of p300 and HDAC1. At IC50 concentration, expression of p300 and HDAC1 mRNA and protein level decreased with time-dependent manner, difference between tested and control groups was significant (P < 0.05). It is concluded that the curcumin can inhibit proliferation of B-NHL Raji cells and promote apoptosis of those cells. Curcumin can inhibit the activity and expression of the transcriptional co-activator p300 and HDAC1, which may be involved in its pharmacological mechanisms on B lymphoma cells.
本研究旨在探讨姜黄素对B-NHL Raji细胞系增殖的影响,并探讨这种影响与p300和HDAC1转录调控表达之间的关系。将体外培养的Raji细胞用不同浓度(6.25 - 50 μmol/L)的姜黄素处理,并在不同时间点(0、6、12、24和48小时)进行处理,通过MTT法测定细胞生长抑制率,采用Annexin V-FITC/PI双染流式细胞术检测细胞凋亡率,通过RT-PCR和Western blot检测Raji细胞中p300和HDAC1 mRNA表达及蛋白水平的变化。结果表明,姜黄素能以显著的时间和浓度依赖性方式抑制Raji细胞增殖,24小时的IC50为25 μmol/L;姜黄素能以浓度依赖性方式诱导Raji细胞凋亡,凋亡率为14.38% - 61.18%。姜黄素显著抑制p300和HDAC1的活性和表达。在IC50浓度下,p300和HDAC1 mRNA表达及蛋白水平随时间呈下降趋势,试验组与对照组差异有统计学意义(P < 0.05)。结论是,姜黄素可抑制B-NHL Raji细胞增殖并促进其凋亡。姜黄素可抑制转录共激活因子p300和HDAC1的活性和表达,这可能参与其对B淋巴瘤细胞的药理作用机制。