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靶向急性髓系白血病中的染色质修饰复合物

Targeting chromatin modifying complexes in acute myeloid leukemia.

作者信息

Schurer Alexandra, Glushakow-Smith Shira G, Gritsman Kira

机构信息

Department of Cell Biology, Albert Einstein College of Medicine, Bronx, NY 10461, United States.

The Ruth L. and David S. Gottesman Institute for Stem Cell Research and Regenerative Medicine, Albert Einstein College of Medicine, Bronx, NY 10461, United States.

出版信息

Stem Cells Transl Med. 2025 Feb 11;14(2). doi: 10.1093/stcltm/szae089.

Abstract

Acute myeloid leukemia (AML) is a devastating hematologic malignancy with high rates of relapse, which can, in part, be attributed to the dysregulation of chromatin modifications. These epigenetic modifications can affect the capacity of hematopoietic cells to self-renew or differentiate, which can lead to transformation. Aberrant histone modifications contribute to the derepression of self-renewal genes such as HOXA/B and MEIS1 in committed hematopoietic progenitors, which is considered a key mechanism of leukemogenesis in MLL-rearranged (MLL-r) and NPM1-mutated AML. As regulators of some of the key histone modifications in this disease, the menin-KMT2A and polycomb repressive (PRC1/2) complexes have been identified as promising targets for the treatment of AML. This review explores recent discoveries of how leukemic cells hijack these complexes and their interactions with other chromatin regulators to promote disease progression. We also discuss inhibitors targeting these complexes that have demonstrated therapeutic efficacy in preclinical and clinical studies and propose novel therapeutic combinations targeting the KMT2A and PRC1/2 broader interacting networks to overcome issues of resistance to existing monotherapies.

摘要

急性髓系白血病(AML)是一种具有高复发率的毁灭性血液系统恶性肿瘤,其复发部分可归因于染色质修饰的失调。这些表观遗传修饰会影响造血细胞自我更新或分化的能力,进而导致细胞转化。异常的组蛋白修饰会导致已定向的造血祖细胞中自我更新基因(如HOXA/B和MEIS1)的去抑制,这被认为是MLL重排(MLL-r)和NPM1突变型AML白血病发生的关键机制。作为该疾病中一些关键组蛋白修饰的调节因子,Menin-KMT2A和多梳抑制(PRC1/2)复合物已被确定为治疗AML的有前景的靶点。本综述探讨了白血病细胞如何劫持这些复合物以及它们与其他染色质调节因子的相互作用以促进疾病进展的最新发现。我们还讨论了在临床前和临床研究中已显示出治疗效果的靶向这些复合物的抑制剂,并提出了针对KMT2A和PRC1/2更广泛相互作用网络的新型治疗组合,以克服对现有单一疗法产生耐药性的问题。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d43f/11878770/20f32990f742/szae089_iffig1.jpg

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