Kamat Ashish M, Tharakan Sheeja T, Sung Bokyung, Aggarwal Bharat B
Department of Urology, The University of Texas M. D. Anderson Cancer Center, Houston, Texas 77030, USA.
Cancer Res. 2009 Dec 1;69(23):8958-66. doi: 10.1158/0008-5472.CAN-09-2045. Epub 2009 Nov 10.
Although Bacillus Calmette-Guerin (BCG) intravesical therapy is a standard treatment for bladder cancer, eventual failure of response is a major problem. Treatments that can augment BCG therapy are urgently needed. We investigated whether curcumin, a component of Curcuma longa (also called turmeric), has potential to improve the current therapy using in vitro and in vivo MBT-2 murine tumor models. We found that curcumin potentiated BCG-induced apoptosis of human bladder cancer cells. BCG stimulated the release of tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) from peripheral mononuclear neutrophils in a dose- and time-dependent manner, whereas curcumin enhanced the upregulation of TRAIL receptors. Electrophoretic mobility shift assay revealed that curcumin also suppressed the BCG-induced activation of the cell survival transcription factor NF-kappaB. In a syngeneic bladder cancer model, curcumin alone reduced the bladder tumor volume, but a significantly greater reduction was observed when BCG and curcumin were used in combination (P < 0.0001 versus control; P < 0.003 versus BCG alone). This was accompanied by a significant decrease in the proliferation marker Ki-67 (P < 0.01 versus control; P < 0.01 versus BCG alone) and microvessel density (CD31; P < 0.01 versus control; P < 0.01 versus BCG alone), decreased NF-kappaB in tumor tissue compared with the control, induced apoptosis, and decreased cyclin D1, vascular endothelial growth factor, cyclooxygenase-2, c-myc, and Bcl-2 expression in the tumor tissue. Upregulation of TRAIL receptor by the combination was also observed in tumor tissues. Overall, our results suggest that curcumin potentiates the antitumor effect of BCG through the inhibition of NF-kappaB and induction of TRAIL receptors in bladder cancer cells.
尽管卡介苗(BCG)膀胱内灌注疗法是膀胱癌的标准治疗方法,但最终治疗反应失败仍是一个主要问题。迫切需要能够增强卡介苗疗法效果的治疗方法。我们使用体外和体内MBT - 2小鼠肿瘤模型,研究了姜黄(也称为姜黄根粉)的成分姜黄素是否具有改善当前治疗方法的潜力。我们发现姜黄素可增强卡介苗诱导的人膀胱癌细胞凋亡。卡介苗以剂量和时间依赖性方式刺激外周单核中性粒细胞释放肿瘤坏死因子相关凋亡诱导配体(TRAIL),而姜黄素增强了TRAIL受体的上调。电泳迁移率变动分析显示,姜黄素还抑制了卡介苗诱导的细胞存活转录因子NF-κB的激活。在同基因膀胱癌模型中,单独使用姜黄素可减小膀胱肿瘤体积,但当卡介苗与姜黄素联合使用时,观察到肿瘤体积有更显著的减小(与对照组相比,P < 0.0001;与单独使用卡介苗相比,P < 0.003)。这伴随着增殖标志物Ki-67显著降低(与对照组相比,P < 0.01;与单独使用卡介苗相比,P < 0.01)和微血管密度(CD31;与对照组相比,P < 0.01;与单独使用卡介苗相比,P < 0.01)降低,肿瘤组织中NF-κB与对照组相比减少,诱导凋亡,并降低肿瘤组织中细胞周期蛋白D1、血管内皮生长因子、环氧合酶-2、c-myc和Bcl-2的表达。在肿瘤组织中还观察到联合使用时TRAIL受体的上调。总体而言,我们的结果表明,姜黄素通过抑制NF-κB和诱导膀胱癌细胞中的TRAIL受体来增强卡介苗的抗肿瘤作用。