Yu Ziming, Shah Dinesh M
Department of Obstetrics and Gynecology, University of Wisconsin-Madison, 7E-Meriter Hospital, 202 South Park Street, Madison, WI 53715, USA.
Gynecol Oncol. 2007 Sep;106(3):541-8. doi: 10.1016/j.ygyno.2007.05.024. Epub 2007 Jun 27.
Curcumin has been demonstrated to have an anti-tumor activity but the underlying molecular mechanisms are not fully uncovered. The present study was undertaken to determine the effect of curcumin on the expression of the proto-oncogene Ets-1 and the anti-apoptotic molecule Bcl-2 in human endometrial adenocarcinoma HEC-1-A cells.
Confluent HEC-1-A cells were treated with curcumin at various doses for 16 h or at 60 microM for various time points. At the end of the designated treatments, changes in cell morphology, DNA fragmentation and protein contents of Ets-1 and Bcl-2 were determined, respectively, by light microscopy, DNA laddering assay and Western blot analysis. As an initial step towards understanding whether Ets-1 was a possible up-stream regulator of Bcl-2 expression in HEC-1-A cells and if so, whether curcumin could attenuate the Ets-1-induced up-regulation of Bcl-2 expression, cells were transiently transfected with an Ets-1/GFP (Green Fluorescence Protein) fusion construct and the transfectants were treated with 60 microM curcumin for 16 h, followed by whole cell lysate preparation for Western blot analysis of Bcl-2 protein contents.
Curcumin induced apoptosis-like morphological changes and DNA degradation and decreased basal levels of Ets-1 and Bcl-2 protein contents in HEC-1-A cells in a time- and dose-dependent manner. Overexpression of Ets-1 in the cell resulted in an increase in Bcl-2 protein contents and that increase was attenuated by curcumin treatment.
Curcumin down-regulates Ets-1 and Bcl-2 expression and induces apoptosis in HEC-1-A cells, suggesting a novel molecular mechanism for the anti-tumor activity of curcumin.
姜黄素已被证明具有抗肿瘤活性,但其潜在的分子机制尚未完全阐明。本研究旨在确定姜黄素对人子宫内膜腺癌HEC-1-A细胞中原癌基因Ets-1和抗凋亡分子Bcl-2表达的影响。
将汇合的HEC-1-A细胞用不同剂量的姜黄素处理16小时或用60微摩尔姜黄素处理不同时间点。在指定处理结束时,分别通过光学显微镜、DNA梯状条带分析和蛋白质印迹分析来确定细胞形态变化、DNA片段化以及Ets-1和Bcl-2的蛋白质含量变化。作为了解Ets-1是否可能是HEC-1-A细胞中Bcl-2表达的上游调节因子以及如果是,姜黄素是否能减弱Ets-1诱导的Bcl-2表达上调的初步步骤,将细胞用Ets-1/绿色荧光蛋白(GFP)融合构建体进行瞬时转染,然后将转染细胞用60微摩尔姜黄素处理16小时,随后制备全细胞裂解物用于蛋白质印迹分析Bcl-2蛋白质含量。
姜黄素以时间和剂量依赖性方式诱导HEC-1-A细胞出现凋亡样形态变化和DNA降解,并降低Ets-1和Bcl-2蛋白质的基础水平。细胞中Ets-1的过表达导致Bcl-2蛋白质含量增加,而姜黄素处理可减弱这种增加。
姜黄素下调HEC-1-A细胞中Ets-1和Bcl-2的表达并诱导细胞凋亡,提示姜黄素抗肿瘤活性的一种新的分子机制。