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新型蒽环类药物乌托柔比星用于癌症治疗。

Novel Anthracycline Utorubicin for Cancer Therapy.

机构信息

Institute of Biomedicine and Translational Medicine, University of Tartu, Ravila 14b, 50411, Tartu, Estonia.

Toxinvent LLC, Tiigi 61b, 50410, Tartu, Estonia.

出版信息

Angew Chem Int Ed Engl. 2021 Jul 26;60(31):17018-17027. doi: 10.1002/anie.202016421. Epub 2021 Jun 1.

Abstract

Novel anticancer compounds and their precision delivery systems are actively developed to create potent and well-tolerated anticancer therapeutics. Here, we report the synthesis of a novel anthracycline, Utorubicin (UTO), and its preclinical development as an anticancer payload for nanocarriers. Free UTO was significantly more toxic to cultured tumor cell lines than the clinically used anthracycline, doxorubicin. Nanoformulated UTO, encapsulated in polymeric nanovesicles (polymersomes, PS), reduced the viability of cultured malignant cells and this effect was potentiated by functionalization with a tumor-penetrating peptide (TPP). Systemic peptide-guided PS showed preferential accumulation in triple-negative breast tumor xenografts implanted in mice. At the same systemic UTO dose, the highest UTO accumulation in tumor tissue was seen for the TPP-targeted PS, followed by nontargeted PS, and free doxorubicin. Our study suggests potential applications for UTO in the treatment of malignant diseases and encourages further preclinical and clinical studies on UTO as a nanocarrier payload for precision cancer therapy.

摘要

新型抗癌化合物及其精准投递系统正在被积极研发,以创造高效且耐受良好的抗癌疗法。在这里,我们报告了一种新型蒽环类药物,乌托柔比星(UTO)的合成及其作为纳米载体抗癌有效载荷的临床前开发。游离 UTO 对培养的肿瘤细胞系的毒性明显高于临床使用的蒽环类药物多柔比星。包裹在聚合物纳米囊泡(聚合物囊泡,PS)中的纳米化 UTO 降低了培养的恶性细胞的活力,并且这种作用通过与肿瘤穿透肽(TPP)功能化而增强。系统肽引导的 PS 显示在植入小鼠的三阴性乳腺癌异种移植肿瘤中优先积累。在相同的系统 UTO 剂量下,在肿瘤组织中观察到 TPP 靶向 PS 的 UTO 积累最高,其次是非靶向 PS 和游离多柔比星。我们的研究表明 UTO 在治疗恶性疾病方面具有潜在的应用,并鼓励进一步对 UTO 作为精准癌症治疗的纳米载体有效载荷进行临床前和临床研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5406/8362190/11179212aa84/ANIE-60-17018-g003.jpg

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