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青蒿素作为一种抗癌药物:靶标分析和作用机制的最新进展。

Artemisinin as an anticancer drug: Recent advances in target profiling and mechanisms of action.

机构信息

Department of Physiology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.

Department of Biological Sciences, National University of Singapore, Singapore, Singapore.

出版信息

Med Res Rev. 2017 Nov;37(6):1492-1517. doi: 10.1002/med.21446. Epub 2017 Jun 23.

Abstract

Artemisinin and its derivatives (collectively termed as artemisinins) are among the most important and effective antimalarial drugs, with proven safety and efficacy in clinical use. Beyond their antimalarial effects, artemisinins have also been shown to possess selective anticancer properties, demonstrating cytotoxic effects against a wide range of cancer types both in vitro and in vivo. These effects appear to be mediated by artemisinin-induced changes in multiple signaling pathways, interfering simultaneously with multiple hallmarks of cancer. Great strides have been taken to characterize these pathways and to reveal their anticancer mechanisms of action of artemisinin. Moreover, encouraging data have also been obtained from a limited number of clinical trials to support their anticancer property. However, there are several key gaps in knowledge that continue to serve as significant barriers to the repurposing of artemisinins as effective anticancer agents. This review focuses on important and emerging aspects of this field, highlighting breakthroughs in unresolved questions as well as novel techniques and approaches that have been taken in recent studies. We discuss the mechanism of artemisinin activation in cancer, novel and significant findings with regards to artemisinin target proteins and pathways, new understandings in artemisinin-induced cell death mechanisms, as well as the practical issues of repurposing artemisinin. We believe these will be important topics in realizing the potential of artemisinin and its derivatives as safe and potent anticancer agents.

摘要

青蒿素及其衍生物(统称为青蒿素类药物)是最重要和最有效的抗疟药物之一,在临床应用中已被证明安全有效。除了抗疟作用外,青蒿素类药物还具有选择性抗癌特性,在体外和体内对多种癌症类型均显示出细胞毒性作用。这些作用似乎是由青蒿素诱导的多种信号通路变化介导的,同时干扰癌症的多个标志性特征。人们已经做出了巨大的努力来描述这些途径,并揭示青蒿素的抗癌作用机制。此外,从有限数量的临床试验中也获得了令人鼓舞的数据,支持其抗癌特性。然而,仍有几个关键的知识空白继续成为将青蒿素类药物重新用作有效抗癌药物的重大障碍。本综述重点关注该领域的重要和新兴方面,强调解决未决问题的突破以及最近研究中采用的新技术和方法。我们讨论了青蒿素在癌症中的激活机制、青蒿素靶蛋白和途径的新发现、青蒿素诱导的细胞死亡机制的新认识,以及重新利用青蒿素的实际问题。我们相信,这些将是实现青蒿素及其衍生物作为安全有效的抗癌药物的潜力的重要课题。

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