Liu Dongwu, Chen Zhiwei
Analysis and Testing Center, Shandong University of Technology, 255049 Zibo, China.
Anticancer Agents Med Chem. 2009 May;9(4):392-6. doi: 10.2174/1871520610909040392.
Natural product extracts are a rich source of small molecules that display antitumor activity. Cantharidin, in the form of the dried body of the Chinese blister beetles: Mylabris phalerata or M. cichorii, displays antitumor activity and induces apoptosis in many types of tumor cells. Cantharidin has been used as an anticancer agent by the Chinese for the treatment of hepatoma and oesophageal carcinoma for a long time. Although cantharidin is a natural toxin that possesses potent anti-tumor properties, its clinical application is limited due to severe side-effects and highly toxic nature. Therefore, some modified cantharidin analogues are synthesized chemically in order to achieve a comparable antitumour property to the mother compound but simultaneously produce a less toxic effect on non-cancer cells. In recent years, based on the structure of cantharidin, there has been intense interest in developing potent and selective inhibitors of PP1 and PP2A on tumour cells. Though numerous analogues of cantharidin have been synthesized and researched with tumour cell lines, there is little success on clinical application because of the potential toxicity of cantharidin derivates. The focus of this review is to describe how cantharidin and cantharidin derivates participate in antitumour processes in tumour cells, and discuss the molecular mechanisms of cantharidin and cantharidin derivates on tumour cells.
天然产物提取物是具有抗肿瘤活性的小分子的丰富来源。斑蝥素,以中国斑蝥(斑蝥或南方大斑蝥)干燥虫体的形式存在,具有抗肿瘤活性,并能诱导多种肿瘤细胞凋亡。长期以来,斑蝥素被中国人用作抗癌剂来治疗肝癌和食管癌。尽管斑蝥素是一种具有强大抗肿瘤特性的天然毒素,但其临床应用因严重的副作用和高毒性而受到限制。因此,人们通过化学合成一些修饰的斑蝥素类似物,以获得与母体化合物相当的抗肿瘤特性,同时对非癌细胞产生较小的毒性作用。近年来,基于斑蝥素的结构,人们对开发针对肿瘤细胞的高效、选择性PP1和PP2A抑制剂产生了浓厚兴趣。尽管已经合成了许多斑蝥素类似物并在肿瘤细胞系中进行了研究,但由于斑蝥素衍生物的潜在毒性,临床应用几乎没有成功。本综述的重点是描述斑蝥素和斑蝥素衍生物如何参与肿瘤细胞的抗肿瘤过程,并讨论斑蝥素和斑蝥素衍生物对肿瘤细胞的分子机制。