The State Key Laboratory of Medicinal Chemical Biology, College of Pharmacy, and Tianjin Key Laboratory of Molecular Drug Research, Nankai University, Tianjin 300353, China.
Int J Mol Sci. 2023 Mar 8;24(6):5184. doi: 10.3390/ijms24065184.
Eukaryotic elongation factor 1A (eEF1A) canonically delivers amino acyl tRNA to the ribosomal A site during the elongation stage of protein biosynthesis. Yet paradoxically, the oncogenic nature of this instrumental protein has long been recognized. Consistently, eEF1A has proven to be targeted by a wide assortment of small molecules with excellent anticancer activity, among which plitidepsin has been granted approval for the treatment of multiple myeloma. Meanwhile, metarrestin is currently under clinical development for metastatic cancers. Bearing these exciting advances in mind, it would be desirable to present a systematic up-to-date account of the title topic, which, to the best of our knowledge, has thus far been unavailable in the literature. The present review summarizes recent advances in eEF1A-targeting anticancer agents, both naturally occurring and synthetically crafted, with regard to their discovery or design, target identification, structure-activity relationship, and mode of action. Their structural diversity and differential eEF1A-targeting mechanisms warrant continuing research in pursuit of curing eEF1A-driven malignancy.
真核延伸因子 1A(eEF1A)在蛋白质生物合成的延伸阶段将氨酰-tRNA 递送至核糖体 A 位。然而,具有讽刺意味的是,这种工具蛋白的致癌性质早已被认识到。一直以来,eEF1A 已被证明是多种具有优异抗癌活性的小分子的靶标,其中plitidepsin 已被批准用于治疗多发性骨髓瘤。同时,metarrestin 目前正在开发用于转移性癌症的药物。考虑到这些令人兴奋的进展,有必要对标题主题进行系统的最新阐述,据我们所知,迄今为止文献中尚无相关内容。本综述总结了近年来在 eEF1A 靶向抗癌药物方面的进展,包括天然存在的和人工合成的,涉及它们的发现或设计、靶标鉴定、结构-活性关系和作用机制。它们的结构多样性和差异化的 eEF1A 靶向机制需要继续研究,以寻求治愈 eEF1A 驱动的恶性肿瘤。