Yang Huayu, Guo Wei, Xu Bo, Li Min, Cui Jingrong
State Key Laboratory of Natural and Biomimetic Drugs, Peking University Health Science Center, Beijing, PRC.
Anticancer Drugs. 2007 Nov;18(10):1133-7. doi: 10.1097/CAD.0b013e3282eeb1c5.
Norcantharidin (NCTD), a demethylated form of cantharidin, is currently used as an anticancer drug in China, but five newly synthesized derivatives have not been tested for antitumor efficacy. In this study, we investigated the in-vitro and in-vivo activity of five derivatives on Bel-7402, HeLa and PC-3M1E8 cell lines on a sulfarhodamine B assay. All of the derivatives showed significant antiproliferative activity, hence we elected to study further one of them, NCTD-Nd3II, in an in-vivo mouse model, and to examine its effects on cell cycle and protein expression. NCTD-Nd3II inhibited H22 tumors in mice in a dose-dependent manner with low toxicity. Flow cytometry results showed that apoptosis and G2/M cell cycle arrest contributed to the cytotoxic and cytostatic effects of NCTD-Nd3II. Further studies showed that Bax and p21 protein expression was upregulated, whereas cyclin B1, Cdc-2 and Bcl-2 protein expression was downregulated. Our findings show that NCTD-Nd3II might be a promising chemotherapeutic agent for hepatomas.
去甲斑蝥素(NCTD)是斑蝥素的去甲基化形式,目前在中国用作抗癌药物,但五种新合成的衍生物尚未进行抗肿瘤疗效测试。在本研究中,我们通过磺基罗丹明B测定法研究了五种衍生物对Bel-7402、HeLa和PC-3M1E8细胞系的体外和体内活性。所有衍生物均显示出显著的抗增殖活性,因此我们选择在体内小鼠模型中进一步研究其中一种,即NCTD-Nd3II,并研究其对细胞周期和蛋白质表达的影响。NCTD-Nd3II以剂量依赖性方式抑制小鼠H22肿瘤,且毒性较低。流式细胞术结果表明,凋亡和G2/M期细胞周期阻滞导致了NCTD-Nd3II的细胞毒性和细胞抑制作用。进一步研究表明,Bax和p21蛋白表达上调,而细胞周期蛋白B1、Cdc-2和Bcl-2蛋白表达下调。我们的研究结果表明,NCTD-Nd3II可能是一种有前景的肝癌化疗药物。