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乳酸化修饰鉴定KMT2A重排急性髓系白血病中的关键生物标志物和治疗靶点。

Lactylation modulation identifies key biomarkers and therapeutic targets in KMT2A-rearranged AML.

作者信息

Liu Dan, Liu Silu, Ji Yujie, Jin Ziyan, He Zhewei, Hou Mengjia, Li Dongyang, Ma Xiao

机构信息

Soochow Hopes Hematonosis Hospital, Wudong Road 1339, Wuzhong District, Suzhou, 215100, China.

National Clinical Research Center for Hematologic Diseases, Jiangsu Institute of Hematology, The First Affiliated Hospital of Soochow University, Suzhou, China.

出版信息

Sci Rep. 2025 Jan 9;15(1):1511. doi: 10.1038/s41598-025-86136-2.

Abstract

Acute Myeloid Leukemia (AML) with KMT2A rearrangements (KMT2Ar), found on chromosome 11q23, is often called KMT2A-rearranged AML (KMT2Ar-AML). This variant is highly aggressive, characterized by rapid disease progression and poor outcomes. Growing knowledge of epigenetic changes, especially lactylation, has opened new avenues for investigation and management of this subtype. Lactylation plays a significant role in cancer, inflammation, and tissue regeneration, but the underlying mechanisms are not yet fully understood. This research examined the influence of lactylation on gene expression within KMT2Ar-AML, initially identifying twelve notable lactylation-dependent differentially expressed genes (DEGs). Using advanced machine learning techniques, six key lactylation-associated genes (PFN1, S100A6, CBR1, LDHB, LGALS1, PRDX1) were identified as essential for prognostic evaluation and linked to relevant disease pathways. The study also suggested PI3K inhibitors and Pevonedistat as possible therapeutic options to modulate immune cell infiltration. Our findings confirm the critical role of lactylation in KMT2Ar-AML and identify six key genes that may serve as biomarkers for diagnosis and treatment. In addition to highlighting the need for further validation in clinical settings, these findings contribute to our understanding of KMT2Ar-AML's molecular mechanisms.

摘要

11号染色体q23上发现的伴有KMT2A重排(KMT2Ar)的急性髓系白血病(AML),通常称为KMT2A重排AML(KMT2Ar-AML)。这种变体具有高度侵袭性,其特征是疾病进展迅速且预后不良。对表观遗传变化,尤其是乳酰化的认识不断增加,为该亚型的研究和管理开辟了新途径。乳酰化在癌症、炎症和组织再生中发挥着重要作用,但其潜在机制尚未完全了解。本研究考察了乳酰化对KMT2Ar-AML内基因表达的影响,最初鉴定出12个显著的乳酰化依赖性差异表达基因(DEG)。使用先进的机器学习技术,确定了6个关键的乳酰化相关基因(PFN1、S100A6、CBR1、LDHB、LGALS1、PRDX1)对预后评估至关重要,并与相关疾病途径相关。该研究还表明,PI3K抑制剂和pevonedistat可能是调节免疫细胞浸润的治疗选择。我们的研究结果证实了乳酰化在KMT2Ar-AML中的关键作用,并确定了6个可能作为诊断和治疗生物标志物的关键基因。除了强调在临床环境中需要进一步验证外,这些发现有助于我们理解KMT2Ar-AML的分子机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd55/11718094/08e19d03a904/41598_2025_86136_Fig1_HTML.jpg

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