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Phenanthridone Alkaloids of the Amaryllidaceae as Activators of the Apoptosis-related Proteolytic Enzymes, Caspases

机译:Amaryllidaceae的菲亚蒽酮作为凋亡相关蛋白水解酶,胱天蛋白酶的活化剂

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摘要

Apoptosis-inducing anticancer drugs have garnered widespread interest in recent years. Targets which concomitantly also exhibit minimal adverse effects in normal, healthy cells have been particularly well-received. The phenanthridone alkaloids such as pancratistatin and narciclasine exemplify such a class of chemotherapeutics, with potent and selective cytotoxic effects in a wide variety of cancer cells which are manifested via the apoptotic mode of cell death. Caspases are central to the apoptotic process through their key function as effector molecules in apoptosis-related signaling pathways. Any attempt to mediate in such pathways, for example to probe the efficacy or mechanism of action of a drug, would inexorably serve to have a modulatory effect on these proteolytic enzymes. Apoptosis studies of phenanthridone alkaloids of the Amaryllidaceae have only gathered momentum over the past decade, following which caspases have understandably emerged as reliable biochemical markers of the process in an assortment of cancers. This review covers such studies of these alkaloids based on their structural-type, pointing out the various caspases which have been activated in different cancer cells and how structure modification can to a certain extent have a bearing on such activity. Also considered are clues to the apoptosis signaling pathways mediated following phenanthridone-induced activation of caspases.
机译:近年来,诱导凋亡诱导的抗癌药物普遍存在普遍的兴趣。尤其是在正常,健康细胞中表现出最小的不良反应的目标是特别接受的。菲尼酮等生物碱如Pancratistatin和Narciclasine举例说明了一类化学治疗剂,具有有效和选择性的细胞毒性在各种癌细胞中,其表现为通过细胞死亡的凋亡模式表现出来。通过其关键功能作为凋亡相关的信号通路中的效应分子是凋亡过程的凋亡过程中的核酶。任何在这种途径中介导的尝试,例如探测药物的疗效或作用的作用机制,将不可避免地对这些蛋白水解酶进行调节作用。疟原虫植物生物碱的凋亡研究仅在过去十年中聚集了势头,后面的血症酶在各种各样的癌症中可理解的过程中可用的生化标志物。本综述涵盖了基于它们的结构型对这些生物碱的研究,指出在不同癌细胞中被激活的各种胱天蛋白酶以及结构改性如何在一定程度上具有轴承的这种活性。还考虑了介导的培养酮诱导的胱天蛋白酶活化后介导的凋亡信号传导途径的线索。

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