他卡洛内酯微管稳定剂。

Q1 Medicine
Samantha S Yee, Lin Du, April L Risinger
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引用次数: 0

摘要

微管稳定剂是许多实体癌症治疗的支柱,并继续在与分子靶向抗癌药物和免疫疗法的联合治疗中发挥作用。然而,对微管稳定剂的先天和获得性耐药限制了其临床疗效。塔卡内酯是从塔卡植物中分离出来的一类独特的微管稳定剂,可以规避临床相关的耐药机制。虽然最初的报道表明,塔卡洛内酯的微管稳定活性与直接结合微管蛋白无关,但进一步的研究发现,有效的C-22、C-23环氧化塔卡洛内酯与β-微管蛋白的天冬氨酸226残基共价结合,这种相互作用对其微管稳定活性至关重要。与其他微管稳定剂相比,塔卡洛内酯具有不同的特性,它们对微管结构和动力学的生化作用促进了不同的细胞表型。一些他卡洛内酯类药物已经在耐药肿瘤模型中显示出了良好的效力和持久的抗肿瘤功效,这是由于它们的不可逆靶向作用。最近在他卡洛内酯支架上可修饰的位点的鉴定为他卡洛内酯-微管蛋白相互作用的特异性提供了证据。这也为进一步优化他卡洛内酯的靶向递送,进一步提高其抗癌功效和临床开发潜力提供了机会。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Taccalonolide Microtubule Stabilizers.

Microtubule stabilizers are a mainstay in the treatment of many solid cancers and continue to find utility in combination therapy with molecularly targeted anticancer agents and immunotherapeutics. However, innate and acquired resistance to microtubule stabilizers can limit their clinical efficacy. The taccalonolides are a unique class of microtubule stabilizers isolated from plants of Tacca that circumvent clinically relevant mechanisms of drug resistance. Although initial reports suggested that the microtubule-stabilizing activity of the taccalonolides was independent of direct tubulin binding, additional studies have identified that potent C-22, C-23 epoxidized taccalonolides covalently bind the Aspartate 226 residue of β-tubulin and that this interaction is critical for their microtubule-stabilizing activity. The taccalonolides have distinct properties as compared to other microtubule stabilizers with regard to their biochemical effects on tubulin structure and dynamics that promote distinct cellular phenotypes. Some taccalonolides have demonstrated in vivo antitumor efficacy in drug-resistant tumor models with exquisite potency and long-lasting antitumor efficacy as a result of their irreversible target engagement. The recent identification of a site on the taccalonolide scaffold that is amenable to modification has provided evidence of the specificity of the taccalonolide-tubulin interaction. This also affords an opportunity to further optimize the targeted delivery of the taccalonolides to further improve their anticancer efficacy and potential for clinical development.

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CiteScore
4.40
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