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骨髓增殖性肿瘤:等待 JAK2 突变克隆扩增。

Myeloproliferative Neoplasms: The Long Wait for JAK2-Mutant Clone Expansion.

机构信息

Department of Biomedicine, Experimental Hematology, University Hospital Basel and University of Basel, Basel, Switzerland.

Institute of Integrative Biology, ETH Zürich, Zürich, Switzerland.

出版信息

Cell Stem Cell. 2021 Mar 4;28(3):359-361. doi: 10.1016/j.stem.2021.02.018.

DOI:10.1016/j.stem.2021.02.018
PMID:33667352
Abstract

Myeloproliferative neoplasms (MPNs) are hematological malignancies caused by somatic mutations originating from a single hematopoietic stem cell (HSC). In this issue of Cell Stem Cell,Van Egeren et al. (2021) used whole-genome sequencing of hematopoietic colonies to reconstruct the clonal history and time of acquisition of the disease-initiating gene mutation.

摘要

骨髓增殖性肿瘤(MPNs)是由起源于单个造血干细胞(HSC)的体细胞突变引起的血液系统恶性肿瘤。在本期《Cell Stem Cell》杂志上,Van Egeren 等人(2021 年)利用造血集落的全基因组测序来重建疾病起始基因突变的克隆历史和获得时间。

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Myeloproliferative Neoplasms: The Long Wait for JAK2-Mutant Clone Expansion.骨髓增殖性肿瘤:等待 JAK2 突变克隆扩增。
Cell Stem Cell. 2021 Mar 4;28(3):359-361. doi: 10.1016/j.stem.2021.02.018.
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Myeloproliferative neoplasm stem cells.骨髓增殖性肿瘤干细胞
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Molecular insights into regulation of JAK2 in myeloproliferative neoplasms.骨髓增殖性肿瘤中JAK2调控的分子见解
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Clonal analysis of TET2 and JAK2 mutations suggests that TET2 can be a late event in the progression of myeloproliferative neoplasms.TET2 和 JAK2 突变的克隆分析表明,TET2 可能是骨髓增殖性肿瘤进展过程中的晚期事件。
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JAK2 and MPL mutations in myeloproliferative neoplasms.骨髓增殖性肿瘤中的JAK2和MPL突变
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Clonal heterogeneity as a driver of disease variability in the evolution of myeloproliferative neoplasms.克隆异质性作为骨髓增殖性肿瘤演变中疾病变异性的驱动因素。
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JAK2-mutant vascular niche contributes to JAK2 clonal expansion in myeloproliferative neoplasms.JAK2 突变的血管微环境促进骨髓增殖性肿瘤中 JAK2 的克隆性扩增。
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引用本文的文献

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Contributions of bone marrow monocytes/macrophages in myeloproliferative neoplasms with JAK2 mutation.骨髓单核细胞/巨噬细胞在 JAK2 突变的骨髓增殖性肿瘤中的作用。
Ann Hematol. 2023 Jul;102(7):1745-1759. doi: 10.1007/s00277-023-05284-5. Epub 2023 May 26.
2
Case report: Double L611S/V617L mutation in a patient with polycythemia vera originally diagnosed with essential thrombocythemia.病例报告:一名最初诊断为原发性血小板增多症的真性红细胞增多症患者存在双L611S/V617L突变。
Front Oncol. 2022 Nov 22;12:937362. doi: 10.3389/fonc.2022.937362. eCollection 2022.
3
Clonal hematopoiesis in cardiovascular disease and therapeutic implications.
心血管疾病中的克隆性造血及其治疗意义。
Nat Cardiovasc Res. 2022 Feb;1(2):116-124. doi: 10.1038/s44161-021-00015-3. Epub 2022 Feb 7.
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Functional Consequences of Mutations in Myeloproliferative Neoplasms.骨髓增殖性肿瘤中突变的功能后果
Hemasphere. 2021 Jun 1;5(6):e578. doi: 10.1097/HS9.0000000000000578. eCollection 2021 Jun.