Adhami Vaqar Mustafa, Aziz Moammir Hasan, Mukhtar Hasan, Ahmad Nihal
Department of Dermatology, University of Wisconsin, Madison, Wisconsin 53706, USA.
Clin Cancer Res. 2003 Aug 1;9(8):3176-82.
Sanguinarine, derived from the root of Sanguinaria canadensis and other poppy fumaria species, possesses strong antimicrobial, anti-inflammatory, and antioxidant properties. We earlier showed that sanguinarine kills human epidermoid carcinoma A431 cells via an induction of apoptosis [N. Ahmad et al., Clin. Cancer Res., 6: 1524-1528, 2000]. In this study, using immortalized human keratinocytes (HaCaT cells), we provide information about mechanism of the antiproliferative effect of sanguinarine. Sanguinarine [0.1 (M-2 (M)] treatment to HaCaT cells was found to inhibit in a dose-dependent manner the cell proliferation and induce apoptosis, as measured by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay and ELISA, respectively. Sanguinarine treatment also resulted in a significant cleavage of poly(ADP-ribose) polymerase in HaCaT cells. Because mitochondrial pathway is critical for the regulation of apoptosis, we studied the involvement and regulation of mitochondrial events in sanguinarine-mediated apoptosis of HaCaT cells. As shown by the immunoblot analysis, our data clearly demonstrated that sanguinarine treatment to HaCaT cells resulted in a dose-dependent (a) increase in the level of Bax with a concomitant decrease in Bcl-2 levels and (b) increase in Bax/Bcl-2 ratio. Sanguinarine also resulted in significant increases in the proapoptotic members of Bcl-2 family proteins, i.e., Bak and Bid. This was accompanied by increase in (a) protein expression of cytochrome c and apoptotic protease-activating factor-1 and (b) activity and protein expression of caspase-3, caspase-7, caspase-8, and caspase-9. Taken together, our data showed the involvement of mitochondrial pathway and Bcl-2 family proteins during sanguinarine-mediated apoptosis of immortalized keratinocytes. We suggest that sanguinarine could be developed as a drug for the management of hyperproliferative skin disorders, including skin cancer.
血根碱,从加拿大血根草的根以及其他罂粟科紫堇属植物中提取,具有强大的抗菌、抗炎和抗氧化特性。我们之前的研究表明,血根碱通过诱导细胞凋亡来杀死人表皮样癌A431细胞 [N. 艾哈迈德等人,《临床癌症研究》,6: 1524 - 1528,2000]。在本研究中,我们使用永生化人角质形成细胞(HaCaT细胞),提供了有关血根碱抗增殖作用机制的信息。通过3 -(4,5 - 二甲基噻唑 - 2 - 基)- 2,5 - 二苯基四氮唑溴盐法和酶联免疫吸附测定法分别检测发现,用0.1(微摩尔)至2(微摩尔)的血根碱处理HaCaT细胞,能以剂量依赖的方式抑制细胞增殖并诱导凋亡。血根碱处理还导致HaCaT细胞中的聚(ADP - 核糖)聚合酶发生显著裂解。由于线粒体途径对细胞凋亡的调节至关重要,我们研究了线粒体事件在血根碱介导的HaCaT细胞凋亡中的参与情况和调节作用。免疫印迹分析结果表明,我们的数据清楚地显示,用 血根碱处理HaCaT细胞会导致:(a)Bax水平呈剂量依赖性升高,同时Bcl - 2水平降低;(b)Bax/Bcl - 2比值升高。血根碱还导致Bcl - 2家族蛋白中的促凋亡成员,即Bak和Bid显著增加。这伴随着:(a)细胞色素c和凋亡蛋白酶激活因子 - 1的蛋白表达增加;(b)半胱天冬酶 - 3、半胱天冬酶 - 7、半胱天冬酶 - 8和半胱天冬酶 - 9的活性及蛋白表达增加。综上所述,我们的数据表明线粒体途径和Bcl - 2家族蛋白参与了血根碱介导的永生化角质形成细胞凋亡过程。我们认为血根碱有望开发成为一种用于治疗包括皮肤癌在内的过度增殖性皮肤疾病的药物。