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Single-cell profiling identifies aberrant STAT5 activation in myeloid malignancies with specific clinical and biologic correlates.单细胞分析确定了髓系恶性肿瘤中异常的STAT5激活,并与特定的临床和生物学特征相关。
Cancer Cell. 2008 Oct 7;14(4):335-43. doi: 10.1016/j.ccr.2008.08.014.
2
Going with the flow: JAK-STAT signaling in JMML.顺势而为:幼年型粒单核细胞白血病中的JAK-STAT信号传导
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3
Stat5 is critical for the development and maintenance of myeloproliferative neoplasm initiated by Nf1 deficiency.Stat5对于由Nf1缺陷引发的骨髓增殖性肿瘤的发生和维持至关重要。
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4
Aberrant GM-CSF signal transduction pathway in juvenile myelomonocytic leukemia assayed by flow cytometric intracellular STAT5 phosphorylation measurement.通过流式细胞术检测细胞内STAT5磷酸化来分析青少年型骨髓单核细胞白血病中异常的GM-CSF信号转导通路。
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Aberrant phosphorylation of STAT5 by granulocyte-macrophage colony-stimulating factor in infant cytomegalovirus infection mimicking juvenile myelomonocytic leukemia.粒细胞-巨噬细胞集落刺激因子导致婴儿巨细胞病毒感染时 STAT5 异常磷酸化,类似于幼年型粒单核细胞白血病。
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CBL linker region and RING finger mutations lead to enhanced granulocyte-macrophage colony-stimulating factor (GM-CSF) signaling via elevated levels of JAK2 and LYN.CBL 连接区和 RING 指突变通过提高 JAK2 和 LYN 的水平导致增强的粒细胞-巨噬细胞集落刺激因子 (GM-CSF) 信号传导。
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SOCS2: inhibitor of JAK2V617F-mediated signal transduction.细胞因子信号转导抑制因子2:JAK2V617F介导的信号转导抑制剂。
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Leukemogenic Ptpn11 causes fatal myeloproliferative disorder via cell-autonomous effects on multiple stages of hematopoiesis.致白血病的Ptpn11通过对造血多个阶段的细胞自主效应导致致命的骨髓增殖性疾病。
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Functional evaluation of circulating hematopoietic progenitors in Noonan syndrome.Noonan 综合征中循环造血祖细胞的功能评估。
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Biallelic SH2B3 germline variants are associated with a neonatal myeloproliferative disease and multisystemic involvement.双等位基因SH2B3种系变异与新生儿骨髓增殖性疾病和多系统受累相关。
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Eradication of Therapy-Resistant Cancer Stem Cells by Novel Telmisartan Derivatives.新型替米沙坦衍生物对治疗抵抗性癌症干细胞的根除作用
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Distinct roles of hematopoietic cytokines in the regulation of leukemia stem cells in murine MLL-AF9 leukemia.造血细胞因子在调节小鼠 MLL-AF9 白血病中白血病干细胞的作用不同。
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Germline bi-allelic alteration predisposes to a neonatal juvenile myelomonocytic leukemia-like disorder.种系双等位基因改变易患新生儿青少年骨髓单核细胞白血病样疾病。
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7
Phenotypic profiling of CD34 cells by advanced flow cytometry improves diagnosis of juvenile myelomonocytic leukemia.采用高级流式细胞术对 CD34 细胞进行表型分析可提高青少年骨髓单核细胞白血病的诊断率。
Haematologica. 2024 Feb 1;109(2):521-532. doi: 10.3324/haematol.2023.282805.
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Proposals for Clinical Trials in Chronic Myelomonocytic Leukemia.慢性粒单核细胞白血病临床试验建议。
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ABT199/venetoclax potentiates the cytotoxicity of alkylating agents and fludarabine in acute myeloid leukemia cells.ABT199/venetoclax 增强了烷化剂和氟达拉滨在急性髓系白血病细胞中的细胞毒性。
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本文引用的文献

1
Genotype-phenotype correlation in cases of juvenile myelomonocytic leukemia with clonal RAS mutations.伴有克隆性RAS突变的青少年骨髓单核细胞白血病病例的基因型-表型相关性
Blood. 2008 Jan 15;111(2):966-7; author reply 967-8. doi: 10.1182/blood-2007-09-111831.
2
Development of an allele-specific minimal residual disease assay for patients with juvenile myelomonocytic leukemia.针对青少年骨髓单核细胞白血病患者的等位基因特异性微小残留病检测方法的开发。
Blood. 2008 Feb 1;111(3):1124-7. doi: 10.1182/blood-2007-06-093302. Epub 2007 Nov 13.
3
Hematopoietic cytokine receptor signaling.造血细胞因子受体信号传导
Oncogene. 2007 Oct 15;26(47):6724-37. doi: 10.1038/sj.onc.1210757.
4
Classification and diagnosis of myeloproliferative neoplasms: the 2008 World Health Organization criteria and point-of-care diagnostic algorithms.骨髓增殖性肿瘤的分类与诊断:2008年世界卫生组织标准及即时诊断算法
Leukemia. 2008 Jan;22(1):14-22. doi: 10.1038/sj.leu.2404955. Epub 2007 Sep 20.
5
Targeting RAS signaling pathways in juvenile myelomonocytic leukemia.靶向青少年粒单核细胞白血病中的RAS信号通路。
Curr Drug Targets. 2007 Jun;8(6):715-25. doi: 10.2174/138945007780830773.
6
Proposals and rationale for revision of the World Health Organization diagnostic criteria for polycythemia vera, essential thrombocythemia, and primary myelofibrosis: recommendations from an ad hoc international expert panel.世界卫生组织真性红细胞增多症、原发性血小板增多症和原发性骨髓纤维化诊断标准修订提案及理由:一个特设国际专家小组的建议
Blood. 2007 Aug 15;110(4):1092-7. doi: 10.1182/blood-2007-04-083501. Epub 2007 May 8.
7
Spontaneous improvement of hematologic abnormalities in patients having juvenile myelomonocytic leukemia with specific RAS mutations.患有特定RAS突变的青少年粒单核细胞白血病患者血液学异常的自发改善。
Blood. 2007 Jun 15;109(12):5477-80. doi: 10.1182/blood-2006-09-046649. Epub 2007 Mar 1.
8
Myeloproliferative disease induced by TEL-PDGFRB displays dynamic range sensitivity to Stat5 gene dosage.由TEL-PDGFRB诱导的骨髓增殖性疾病对Stat5基因剂量表现出动态范围敏感性。
Blood. 2007 May 1;109(9):3906-14. doi: 10.1182/blood-2006-07-036335. Epub 2007 Jan 11.
9
K-RasG12D expression induces hyperproliferation and aberrant signaling in primary hematopoietic stem/progenitor cells.K-RasG12D表达可诱导原代造血干细胞/祖细胞过度增殖及异常信号传导。
Blood. 2007 May 1;109(9):3945-52. doi: 10.1182/blood-2006-09-047530. Epub 2006 Dec 27.
10
JAK2 V617F mutation is a rare event in juvenile myelomonocytic leukemia.JAK2 V617F突变在青少年骨髓单核细胞白血病中是一个罕见事件。
Leukemia. 2007 Feb;21(2):367-9. doi: 10.1038/sj.leu.2404484. Epub 2006 Dec 7.

单细胞分析确定了髓系恶性肿瘤中异常的STAT5激活,并与特定的临床和生物学特征相关。

Single-cell profiling identifies aberrant STAT5 activation in myeloid malignancies with specific clinical and biologic correlates.

作者信息

Kotecha Nikesh, Flores Nikki J, Irish Jonathan M, Simonds Erin F, Sakai Debbie S, Archambeault Sophie, Diaz-Flores Ernesto, Coram Marc, Shannon Kevin M, Nolan Garry P, Loh Mignon L

机构信息

Department of Microbiology and Immunology, Stanford University School of Medicine, Stanford, CA 94305, USA.

出版信息

Cancer Cell. 2008 Oct 7;14(4):335-43. doi: 10.1016/j.ccr.2008.08.014.

DOI:10.1016/j.ccr.2008.08.014
PMID:18835035
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2647559/
Abstract

Progress in understanding the molecular pathogenesis of human myeloproliferative disorders (MPDs) has led to guidelines incorporating genetic assays with histopathology during diagnosis. Advances in flow cytometry have made it possible to simultaneously measure cell type and signaling abnormalities arising as a consequence of genetic pathologies. Using flow cytometry, we observed a specific evoked STAT5 signaling signature in a subset of samples from patients suspected of having juvenile myelomonocytic leukemia (JMML), an aggressive MPD with a challenging clinical presentation during active disease. This signature was a specific feature involving JAK-STAT signaling, suggesting a critical role of this pathway in the biological mechanism of this disorder and indicating potential targets for future therapies.

摘要

在理解人类骨髓增殖性疾病(MPD)分子发病机制方面取得的进展,已促使在诊断过程中将基因检测与组织病理学相结合形成指南。流式细胞术的进步使得同时测量因基因病变而产生的细胞类型和信号异常成为可能。通过流式细胞术,我们在疑似患有青少年粒单核细胞白血病(JMML)的患者样本子集中观察到一种特定的诱发STAT5信号特征,JMML是一种侵袭性MPD,在疾病活跃期临床表现具有挑战性。这种特征是涉及JAK-STAT信号传导的一个特定特点,表明该通路在这种疾病的生物学机制中起关键作用,并为未来治疗指明了潜在靶点。