Ravindran Jayaraj, Prasad Sahdeo, Aggarwal Bharat B
Cytokine Research Laboratory, Department of Experimental Therapeutics, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
AAPS J. 2009 Sep;11(3):495-510. doi: 10.1208/s12248-009-9128-x. Epub 2009 Jul 10.
Cancer is a hyperproliferative disorder that is usually treated by chemotherapeutic agents that are toxic not only to tumor cells but also to normal cells, so these agents produce major side effects. In addition, these agents are highly expensive and thus not affordable for most. Moreover, such agents cannot be used for cancer prevention. Traditional medicines are generally free of the deleterious side effects and usually inexpensive. Curcumin, a component of turmeric (Curcuma longa), is one such agent that is safe, affordable, and efficacious. How curcumin kills tumor cells is the focus of this review. We show that curcumin modulates growth of tumor cells through regulation of multiple cell signaling pathways including cell proliferation pathway (cyclin D1, c-myc), cell survival pathway (Bcl-2, Bcl-xL, cFLIP, XIAP, c-IAP1), caspase activation pathway (caspase-8, 3, 9), tumor suppressor pathway (p53, p21) death receptor pathway (DR4, DR5), mitochondrial pathways, and protein kinase pathway (JNK, Akt, and AMPK). How curcumin selectively kills tumor cells, and not normal cells, is also described in detail.
癌症是一种细胞过度增殖性疾病,通常采用化学治疗药物进行治疗,这些药物不仅对肿瘤细胞有毒性,对正常细胞也有毒性,因此这些药物会产生严重的副作用。此外,这些药物价格高昂,大多数人难以承受。而且,这类药物不能用于癌症预防。传统药物通常没有有害的副作用,而且通常价格低廉。姜黄素是姜黄(Curcuma longa)的一种成分,就是这样一种安全、实惠且有效的药物。姜黄素如何杀死肿瘤细胞是本综述的重点。我们表明,姜黄素通过调节多种细胞信号通路来调节肿瘤细胞的生长,这些信号通路包括细胞增殖通路(细胞周期蛋白D1、c-myc)、细胞存活通路(Bcl-2、Bcl-xL、cFLIP、XIAP、c-IAP1)、半胱天冬酶激活通路(半胱天冬酶-8、3、9)、肿瘤抑制通路(p53、p21)、死亡受体通路(DR4、DR5)、线粒体通路以及蛋白激酶通路(JNK、Akt和AMPK)。本文还详细描述了姜黄素如何选择性地杀死肿瘤细胞而不是正常细胞。