Department of Pharmacy, "G. d'Annunzio" University of Chieti-Pescara, Via dei Vestini 31, 66100, Chieti, Italy.
Department of Pharmacy, "G. d'Annunzio" University of Chieti-Pescara, Via dei Vestini 31, 66100, Chieti, Italy.
Eur J Med Chem. 2025 Jan 5;281:117021. doi: 10.1016/j.ejmech.2024.117021. Epub 2024 Oct 31.
Since their discovery from natural sources, the potent cytotoxic effects of combretastatins were widely studied for the application in antitumor therapy. However, major pharmacokinetic issues as low water solubility and chemical instability of the double bond configuration prevented their use in therapy. A lot of efforts have been directed towards the search of novel strategies, allowing a safer use of combretastatins as anticancer agents. This review analyses the recent landscape in combretastatin research, characterized by the identification of hybrids, prodrugs, and novel combination treatments. Interestingly, the potent cytotoxic agent combretastatin A4 (CA4) was recently proposed as payload in the construction of novel antibody-drug conjugates (ADCs), allowing an efficient targeting of the cytotoxic agent to specific tumors.
自天然来源发现以来,由于其强大的细胞毒性作用,康普瑞汀已被广泛研究用于抗肿瘤治疗。然而,低水溶性和双键构型的化学不稳定性等主要药代动力学问题阻止了它们在治疗中的应用。人们已经投入了大量的努力来寻找新的策略,以使康普瑞汀作为抗癌药物更安全地使用。这篇综述分析了康普瑞汀研究的最新进展,其特点是鉴定了杂种、前药和新的联合治疗方法。有趣的是,强效细胞毒剂康普瑞汀 A4(CA4)最近被提议作为新型抗体药物偶联物(ADC)的有效载荷,使细胞毒性剂能够有效地靶向特定肿瘤。