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姜黄素下调Notch-1与抑制胰腺癌细胞生长及诱导其凋亡有关。

Notch-1 down-regulation by curcumin is associated with the inhibition of cell growth and the induction of apoptosis in pancreatic cancer cells.

作者信息

Wang Zhiwei, Zhang Yuxiang, Banerjee Sanjeev, Li Yiwei, Sarkar Fazlul H

机构信息

Department of Pathology, Karmanos Cancer Institute, Wayne State University School of Medicine, Detroit, Michigan 48201, USA.

出版信息

Cancer. 2006 Jun 1;106(11):2503-13. doi: 10.1002/cncr.21904.

Abstract

BACKGROUND

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.

METHODS

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.

RESULTS

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.

CONCLUSIONS

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.

摘要

背景

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。

方法

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。

结果

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。

结论

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。

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