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ASXL1、SRSF2和EZH2突变在骨髓增生异常肿瘤和急性髓系白血病染色质失调中的作用。

The role of ASXL1, SRSF2, and EZH2 mutations in chromatin dysregulation of myelodysplastic neoplasia and acute myeloid leukemia.

作者信息

Yu Hosang, Hong Junshik, Shin Dong-Yeop, Lee Chul-Hwan

机构信息

Department of Pharmacology, Seoul National University College of Medicine, Seoul, Republic of Korea.

Department of Biomedical Sciences, Seoul National University College of Medicine, Seoul, Republic of Korea.

出版信息

Leukemia. 2025 Jun 25. doi: 10.1038/s41375-025-02657-9.

Abstract

Mutations in chromatin-regulating genes play a critical role in the pathogenesis of myelodysplastic neoplasia (MDS) and acute myeloid leukemia (AML), as genetic mutations affecting chromatin structure and function are key drivers of these hematologic malignancies. Central to the discussion are key emerging genes such as ASXL1, SRSF2, and EZH2, which are recognized as adverse prognostic markers. Mutations in these genes, coupled with subsequent alterations in epigenetic mechanisms, disrupt normal gene expression by impairing histone modification and RNA splicing processes. Specifically, mutations in ASXL1 enhance removal of ubiquitylation at histone H2AK119, leading to altered gene expression and impaired hematopoietic stem cell differentiation. Mutations in SRSF2, an RNA splicing factor, alter RNA-binding specificity, inducing aberrant splicing of key genes such as EZH2. Loss-of-function mutations in EZH2 disrupt PRC2-mediated transcriptional repression, promoting leukemic progression. However, while the effects of these mutations are understood, treatment options for high-risk patients remain limited. Emerging strategies, such as venetoclax combined with hypomethylating agents, showing promise in mitigating the poor prognosis associated with these mutations. This review consolidates recent findings on these epigenetic regulators and their interactions, providing insights into the multifaceted mechanisms of leukemogenesis in the interest of inspiring targeted therapeutic strategies and bridging extant treatment gaps for MDS/AML.

摘要

染色质调节基因的突变在骨髓增生异常综合征(MDS)和急性髓系白血病(AML)的发病机制中起着关键作用,因为影响染色质结构和功能的基因突变是这些血液系统恶性肿瘤的关键驱动因素。讨论的核心是一些新出现的关键基因,如ASXL1、SRSF2和EZH2,它们被认为是不良预后标志物。这些基因的突变,再加上随后表观遗传机制的改变,通过损害组蛋白修饰和RNA剪接过程来破坏正常基因表达。具体而言,ASXL1的突变增强了组蛋白H2AK119上泛素化的去除,导致基因表达改变和造血干细胞分化受损。RNA剪接因子SRSF2的突变改变了RNA结合特异性,诱导关键基因如EZH2的异常剪接。EZH2的功能丧失突变破坏了PRC2介导的转录抑制,促进白血病进展。然而,尽管这些突变的影响已为人所知,但高危患者的治疗选择仍然有限。新兴策略,如维奈克拉联合低甲基化药物,在改善与这些突变相关的不良预后方面显示出前景。本综述总结了关于这些表观遗传调节因子及其相互作用的最新发现,为白血病发生的多方面机制提供了见解,以期激发靶向治疗策略并弥合MDS/AML现有治疗差距。

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