Wang Fang, Yang Zhe, Wu Yujie, Bai Huanrong, Xin Minhang
Department of Pharmacy & Health Management, Hebei Chemical & Pharmaceutical College, Shijiazhuang, Hebei, P.R. China.
School of Pharmacy, Health Science Center, Xi'an Jiaotong University, Xi'an, Shaanxi, P.R. China.
Expert Opin Ther Pat. 2025 Jan;35(1):65-78. doi: 10.1080/13543776.2024.2422380. Epub 2024 Nov 3.
Acute leukemia harboring rearrangement of the Mixed lineage leukemia (MLL) and/or mutation of the nucleophosmin is a type of poorly prognostic and highly malignant leukemia which is extremely difficult to treat. Blocking the protein-protein interaction between Menin and MLL is a strategic approach for treating leukemias, as a new direction for drug discovery. Many biotech and pharmaceutical companies made great efforts to this drug development field, and a large number of small molecular Menin-MLL PPI inhibitors were reported during the recent three years.
This review is to mainly summarize the Menin-MLL PPI inhibitors reported in the recent three years' patents.
Although the past 12 years have witnessed the progress of the Menin-MLL PPI inhibitors in the treatment of acute leukemia, especially for leukemia harboring rearranged KMT2A and/or mutated NPM1, recent studies showed Menin-MLL PPI inhibitors suffered from new issues such as toxicity, acquired resistance, and homogenization. Therefore, new drug discovery strategies should be considered in advance. The expert opinion was proposed from several aspects, such as developing diverse chemical structures, discovering covalent inhibitors, designing small molecular PROTACs, and targeting the amino acids mutations for next-generation inhibitors.
伴有混合谱系白血病(MLL)重排和/或核仁磷酸蛋白突变的急性白血病是一种预后较差、恶性程度高且极难治疗的白血病。阻断Menin与MLL之间的蛋白质-蛋白质相互作用是治疗白血病的一种策略性方法,也是药物研发的一个新方向。许多生物技术和制药公司在这个药物研发领域付出了巨大努力,在最近三年报道了大量小分子Menin-MLL蛋白-蛋白相互作用抑制剂。
本综述主要总结最近三年专利中报道的Menin-MLL蛋白-蛋白相互作用抑制剂。
尽管在过去12年里,Menin-MLL蛋白-蛋白相互作用抑制剂在急性白血病治疗方面取得了进展,尤其是对于伴有KMT2A重排和/或NPM1突变的白血病,但最近的研究表明,Menin-MLL蛋白-蛋白相互作用抑制剂出现了毒性、获得性耐药和同质化等新问题。因此,应提前考虑新的药物研发策略。从开发多样化化学结构、发现共价抑制剂、设计小分子PROTAC以及针对下一代抑制剂的氨基酸突变等几个方面提出了专家观点。