National Health Commission Key Laboratory of Molecular Probes and Targeted Diagnosis and Therapy, Harbin Medical University, Harbin 150001, China.
Department of Urology, The Fourth Affiliated Hospital of Harbin Medical University, Harbin 150001, China.
Molecules. 2023 Mar 28;28(7):3026. doi: 10.3390/molecules28073026.
Encoded by the gene, menin protein is a fusion protein that is essential for the oncogenic transformation of mixed-lineage leukemia (MLL) and leads to acute leukemia (AL). Therefore, accumulating evidence has demonstrated that inhibition of the high-affinity relationship between menin and mixed-lineage leukemia 1 (MLL1 and KMT2A) is an effective treatment for MLL-rearranged (MLL-r) leukemia in vitro and in vivo. Meanwhile, recent studies found that menin-MLL1 interaction inhibitors exhibited a firm tumor suppressive ability in specific cancer cells, such as prostate cancer, breast cancer, liver cancer, and lung cancer. Overall, it seems to serve as a novel therapeutic means for cancers. Herein, we review the recent progress in exploring the inhibitors of small molecule menin-MLL1 interactions. The molecular mechanisms of these inhibitors' functions and their application prospects in the treatment of AL and cancers are explored.
由 基因编码的 menin 蛋白是一种融合蛋白,对于混合谱系白血病(MLL)的致癌转化至关重要,并导致急性白血病(AL)。因此,越来越多的证据表明,抑制 menin 和混合谱系白血病 1(MLL1 和 KMT2A)之间的高亲和力关系是体外和体内治疗 MLL 重排(MLL-r)白血病的有效方法。同时,最近的研究发现,menin-MLL1 相互作用抑制剂在特定癌细胞(如前列腺癌、乳腺癌、肝癌和肺癌)中表现出坚定的肿瘤抑制能力。总的来说,它似乎为癌症提供了一种新的治疗手段。本文综述了小分子 menin-MLL1 相互作用抑制剂的最新研究进展。探讨了这些抑制剂的功能的分子机制及其在治疗 AL 和癌症中的应用前景。