Wang Zhiwei, Zhang Yuxiang, Banerjee Sanjeev, Li Yiwei, Sarkar Fazlul H
Department of Pathology, Karmanos Cancer Institute, Wayne State University School of Medicine, Detroit, Michigan 48201, USA.
Cancer. 2006 Jun 1;106(11):2503-13. doi: 10.1002/cncr.21904.
Notch signaling plays a critical role in maintaining the balance between cell proliferation, differentiation, and apoptosis, and thereby may contribute to the development of pancreatic cancer. Therefore, the down-regulation of Notch signaling may be a novel approach for pancreatic cancer therapy. It has been reported that curcumin down-regulates many genes that are known to promote survival and also up-regulates genes that are known promoters of apoptosis in pancreatic cancer cells in vitro. It also has been reported that there is cross-talk between Notch-1 and another major cell growth and apoptotic regulatory pathway, the nuclear factor kappaB (NF-kappaB) pathway, which is down-regulated by both curcumin and reduction of Notch-1 levels. However, to the authors' knowledge to date, no studies have determined whether the down-regulation of Notch-1 signaling, resulting in the inactivation of NF-kappaB activity, contributes to curcumin-induced cell growth inhibition and apoptosis in pancreatic cancer cells.
The authors used multiple molecular approaches, such as the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay, an apoptosis assay, gene transfection, real-time reverse transcriptase-polymerase chain reaction analysis, Western blot analysis, and an electrophoretic mobility shift assay to measure the DNA binding activity of NF-kappaB.
Curcumin inhibited cell growth and induced apoptosis in pancreatic cancer cells. Notch-1, Hes-1, and Bcl-XL expression levels concomitantly were down-regulated by curcumin treatment. These results correlated with the inactivation of NF-kappaB activity and increased apoptosis induced by curcumin. The down-regulation of Notch-1 by small-interfering RNA prior to curcumin treatment resulted in enhanced cell growth inhibition and apoptosis.
The current results provide the first demonstration to the authors' knowledge that the Notch-1 signaling pathway is associated mechanistically with NF-kappaB activity during curcumin-induced cell growth inhibition and apoptosis of pancreatic cells. These results suggest that the down-regulation of Notch signaling by curcumin may be a novel strategy for the treatment of patients with pancreatic cancer.
Notch信号通路在维持细胞增殖、分化和凋亡之间的平衡中起关键作用,因此可能与胰腺癌的发生发展有关。所以,下调Notch信号通路可能是一种治疗胰腺癌的新方法。据报道,姜黄素在体外可下调许多已知的促进细胞存活的基因,并上调已知的胰腺癌细胞凋亡促进基因。也有报道称,Notch-1与另一条主要的细胞生长和凋亡调节通路——核因子κB(NF-κB)通路之间存在相互作用,姜黄素和降低Notch-1水平均可下调该通路。然而,据作者所知,迄今为止尚无研究确定Notch-1信号通路的下调是否会导致NF-κB活性失活,从而促进姜黄素诱导的胰腺癌细胞生长抑制和凋亡。
作者采用了多种分子方法,如3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四氮唑溴盐(MTT)法、凋亡检测、基因转染、实时逆转录聚合酶链反应分析、蛋白质免疫印迹分析以及电泳迁移率变动分析来检测NF-κB的DNA结合活性。
姜黄素抑制胰腺癌细胞生长并诱导其凋亡。姜黄素处理后,Notch-1、Hes-1和Bcl-XL的表达水平同时下调。这些结果与NF-κB活性失活以及姜黄素诱导的凋亡增加相关。在姜黄素处理前用小干扰RNA下调Notch-1可增强细胞生长抑制和凋亡。
据作者所知,目前的结果首次证明在姜黄素诱导胰腺细胞生长抑制和凋亡过程中,Notch-1信号通路与NF-κB活性在机制上相关。这些结果表明,姜黄素下调Notch信号通路可能是治疗胰腺癌患者的一种新策略。