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急性髓系白血病中乳酸化和液-液相分离相关基因的潜在预后价值及免疫图谱

Potential prognostic value and immune landscape of lactylation and liquid-liquid phase separation related genes in acute myeloid leukemia.

作者信息

Jiang Tingxiu, Chen Hong, Qin Chunjie, Xie Guoran, Huang Qiumei, Chen Shaomei, Lai Yongrong

机构信息

Department of Hematology, The First Affiliated Hospital of Guangxi Medical University, Nanning, People's Republic of China.

Department of Hematology, The Fourth Affiliated Hospital of Guangxi Medical University, Liuzhou, People's Republic of China.

出版信息

Hematology. 2025 Dec;30(1):2548073. doi: 10.1080/16078454.2025.2548073. Epub 2025 Sep 1.

Abstract

OBJECTIVES

Lactylation- and liquid-liquid phase separation-related differentially expressed genes (LLRDEGs) have been implicated in cancer. However, their role in acute myeloid leukemia (AML) remains largely unexplored.

METHODS

LLRDEGs associated with AML prognosis were identified using Cox regression and LASSO analyzes. A prognostic model based on three LLRDEGs was constructed for AML, and its associated biological functions were investigated. Furthermore, we evaluated differences in the tumor immune microenvironment based on this prognostic signature.

RESULTS

This study represents the first comprehensive analysis of the prognostic value of LLRDEGs in AML patients, identifying three LLRDEGs with prognostic significance. A prognostic risk model was constructed using these three LLRDEGs, and its prognostic value was validated in an independent external AML dataset. This model was associated with the immune microenvironment of AML. Finally, we observed that chaperonin containing TCP1 subunit 5 (CCT5) was highly expressed in AML. In vitro experiments demonstrated that inhibition of CCT5 induces HL-60 cell cycle arrest and apoptosis.

CONCLUSION

This research provides a theoretical basis relevant to AML treatment strategies.

摘要

目的

乳酸化和液-液相分离相关的差异表达基因(LLRDEGs)与癌症有关。然而,它们在急性髓系白血病(AML)中的作用在很大程度上仍未被探索。

方法

使用Cox回归和LASSO分析确定与AML预后相关的LLRDEGs。构建了一个基于三个LLRDEGs的AML预后模型,并研究了其相关的生物学功能。此外,我们基于这个预后特征评估了肿瘤免疫微环境的差异。

结果

本研究首次对LLRDEGs在AML患者中的预后价值进行了全面分析,确定了三个具有预后意义的LLRDEGs。使用这三个LLRDEGs构建了一个预后风险模型,并在独立的外部AML数据集中验证了其预后价值。该模型与AML的免疫微环境相关。最后,我们观察到含TCP1亚基5的伴侣蛋白(CCT5)在AML中高表达。体外实验表明,抑制CCT5可诱导HL-60细胞周期停滞和凋亡。

结论

本研究为AML治疗策略提供了理论依据。

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