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靶向LMO2诱导的自分泌FLT3信号传导以克服早期T细胞前体急性淋巴细胞白血病的化疗耐药性。

Targeting LMO2-induced autocrine FLT3 signaling to overcome chemoresistance in early T-cell precursor acute lymphoblastic leukemia.

作者信息

Tremblay Cedric S, Saw Jesslyn, Yan Feng, Boyle Jacqueline A, Amarasinghe Ovini, Abdollahi Shokoufeh, Vo Anh N Q, Shields Benjamin J, Mayoh Chelsea, McCalmont Hannah, Evans Kathryn, Steiner Anna, Parsons Kevin, McCormack Matthew P, Powell David R, Wong Nicholas C, Jane Stephen M, Lock Richard B, Curtis David J

机构信息

Department of Immunology, Max Rady College of Medicine, University of Manitoba, Winnipeg, MB, Canada.

Paul Albrechtsen Research Institute CancerCare Manitoba, Winnipeg, MB, Canada.

出版信息

Leukemia. 2025 Mar;39(3):577-589. doi: 10.1038/s41375-024-02491-5. Epub 2025 Jan 23.

Abstract

Early T-cell Precursor Acute Lymphoblastic Leukemia (ETP-ALL) is an immature subtype of T-cell acute lymphoblastic leukemia (T-ALL) commonly show deregulation of the LMO2-LYL1 stem cell transcription factors, activating mutations of cytokine receptor signaling, and poor early response to intensive chemotherapy. Previously, studies of the Lmo2 transgenic mouse model of ETP-ALL identified a population of stem-like T-cell progenitors with long-term self-renewal capacity and intrinsic chemotherapy resistance linked to cellular quiescence. Here, analyses of Lmo2 transgenic mice, patient-derived xenografts, and single-cell RNA-sequencing data from primary ETP-ALL identified a rare subpopulation of leukemic stem cells expressing high levels of the cytokine receptor FLT3. Despite a highly proliferative state, these FLT3-overexpressing cells had long-term self-renewal capacity and almost complete resistance to chemotherapy. Chromatin immunoprecipitation and assay for transposase-accessible chromatin sequencing demonstrated FLT3 and its ligand may be direct targets of the LMO2 stem-cell complex. Media conditioned by Lmo2 transgenic thymocytes revealed an autocrine FLT3-dependent signaling loop that could be targeted by the FLT3 inhibitor gilteritinib. Consequently, gilteritinib impaired in vivo growth of ETP-ALL and improved the sensitivity to chemotherapy. Furthermore, gilteritinib enhanced response to the BCL2 inhibitor venetoclax, which may enable "chemo-free" treatment of ETP-ALL. Together, these data provide a cellular and molecular explanation for enhanced cytokine signaling in LMO2-driven ETP-ALL beyond activating mutations and a rationale for clinical trials of FLT3 inhibitors in ETP-ALL.

摘要

早期T细胞前体急性淋巴细胞白血病(ETP-ALL)是T细胞急性淋巴细胞白血病(T-ALL)的一种不成熟亚型,通常表现为LMO2-LYL1干细胞转录因子失调、细胞因子受体信号传导的激活突变以及对强化化疗的早期反应不佳。此前,对ETP-ALL的Lmo2转基因小鼠模型的研究确定了一群具有长期自我更新能力和与细胞静止相关的内在化疗抗性的干细胞样T细胞祖细胞。在此,对Lmo2转基因小鼠、患者来源的异种移植物以及原发性ETP-ALL的单细胞RNA测序数据的分析确定了一个表达高水平细胞因子受体FLT3的罕见白血病干细胞亚群。尽管处于高度增殖状态,但这些FLT3过表达细胞具有长期自我更新能力且几乎对化疗完全耐药。染色质免疫沉淀和转座酶可及染色质测序分析表明,FLT3及其配体可能是LMO2干细胞复合体的直接靶点。由Lmo2转基因胸腺细胞条件培养基揭示了一个自分泌的FLT3依赖性信号环,该信号环可被FLT3抑制剂吉瑞替尼靶向。因此,吉瑞替尼损害了ETP-ALL的体内生长并提高了对化疗的敏感性。此外,吉瑞替尼增强了对BCL2抑制剂维奈克拉的反应,这可能使ETP-ALL能够进行“无化疗”治疗。总之,这些数据为LMO2驱动的ETP-ALL中细胞因子信号增强提供了细胞和分子解释,超出了激活突变,并为ETP-ALL中FLT3抑制剂的临床试验提供了理论依据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/61bc/11879882/34ffe97ec974/41375_2024_2491_Fig1_HTML.jpg

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