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Recent Advances in the Development of New Auristatins: Structural Modifications and Application in Antibody Drug Conjugates

机译:新耳他汀开发的最新进展:结构修饰和在抗体药物偶联物中的应用

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摘要

Dolastatin 10 is a powerful antineoplastic agent and microtubule inhibitor that was discovered by Pettit et al. and published in 1987. Since then, many research groups have engaged in SAR studies of synthetic analogues, termed "auristatins". It was eventually discovered that auristatins are of great value as payloads in antibody drug conjugates (ADCs), which led to the FDA-approved ADC brentuximab vedotin (Seattle Genetics). Currently, over 30 ADCs in clinical trials employ auristatins as payloads, and there is a great interest in the research community, both on academic and industrial sides, to further study these analogues. This review will provide an overview of the recent advancements in auristatin development spanning a time frame of about the past ten years. The main focus will be to describe structural changes made to the auristatin peptide and their resulting biological activities in tumor cell proliferation assays. Selected ADC examples will also be described.
机译:Dolastatin 10是一种强大的抗肿瘤药和微管抑制剂,被Pettit等人发现。并于1987年出版。从那时起,许多研究小组就对合成类似物称为“ auristatins”进行了SAR研究。最终发现,澳瑞他汀作为抗体药物偶联物(ADC)中的有效载荷具有巨大价值,这导致了FDA批准的ADC brentuximab vedotin(西雅图遗传学)。目前,在临床试验中有30多个ADC使用auristatin作为有效载荷,学术界和工业界对研究界都怀着极大的兴趣进一步研究这些类似物。这篇综述将概述过去十年中澳瑞他汀开发的最新进展。主要焦点将是描述在肿瘤细胞增殖测定中对澳瑞他汀肽进行的结构变化及其产生的生物学活性。还将介绍所选的ADC示例。

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