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JAK2 突变。

The JAK2 mutation.

机构信息

Children's Research Institute and the Department of Pediatrics, University of Texas Southwestern Medical Center, Dallas, TX, United States.

出版信息

Int Rev Cell Mol Biol. 2021;365:117-162. doi: 10.1016/bs.ircmb.2021.09.002. Epub 2021 Oct 5.

Abstract

Myeloproliferative neoplasms (MPNs) are clonal hematopoietic stem cell (HSC) disorders with overproduction of mature myeloid blood cells, including essential thrombocythemia (ET), polycythemia vera (PV), and primary myelofibrosis (PMF). In 2005, several groups identified a single gain-of-function point mutation JAK2V617F in the majority of MPN patients. The JAK2V617F mutation confers cytokine independent proliferation to hematopoietic progenitor cells by constitutively activating canonical and non-canonical downstream pathways. In this chapter, we focus on (1) the regulation of JAK2, (2) the molecular mechanisms used by JAK2V617F to induce MPNs, (3) the factors that are involved in the phenotypic diversity in MPNs, and (4) the effects of JAK2V617F on hematopoietic stem cells (HSCs). The discovery of the JAK2V617F mutation led to a comprehensive understanding of MPN; however, the question still remains about how one mutation can give rise to three distinct disease entities. Various mechanisms have been proposed, including JAK2V617F allele burden, differential STAT signaling, and host genetic modifiers. In vivo modeling of JAK2V617F has dramatically enhanced the understanding of the pathophysiology of the disease and provided the pre-clinical platform. Interestingly, most of these models do not show an increased hematopoietic stem cell self-renewal and function compared to wildtype controls, raising the question of whether JAK2V617F alone is sufficient to give a clonal advantage in MPN patients. In addition, the advent of modern sequencing technologies has led to a broader understanding of the mutational landscape and detailed JAK2V617F clonal architecture in MPN patients.

摘要

骨髓增殖性肿瘤(MPN)是克隆性造血干细胞(HSC)疾病,表现为成熟髓系血细胞过度生成,包括原发性血小板增多症(ET)、真性红细胞增多症(PV)和原发性骨髓纤维化(PMF)。2005 年,几个研究小组在大多数 MPN 患者中发现了单一的功能获得性点突变 JAK2V617F。JAK2V617F 突变通过持续激活经典和非经典下游途径,赋予造血祖细胞细胞因子非依赖性增殖能力。在本章中,我们重点介绍(1)JAK2 的调节,(2)JAK2V617F 诱导 MPN 的分子机制,(3)参与 MPN 表型多样性的因素,以及(4)JAK2V617F 对造血干细胞(HSCs)的影响。JAK2V617F 突变的发现使人们对 MPN 有了全面的了解;然而,一个突变如何导致三种不同的疾病实体,这个问题仍然存在。已经提出了各种机制,包括 JAK2V617F 等位基因负担、不同的 STAT 信号转导和宿主遗传修饰物。JAK2V617F 的体内建模极大地增强了对疾病病理生理学的理解,并提供了临床前平台。有趣的是,与野生型对照相比,这些模型中的大多数都没有表现出造血干细胞自我更新和功能的增加,这就提出了一个问题,即 JAK2V617F 本身是否足以在 MPN 患者中获得克隆优势。此外,现代测序技术的出现使人们对 MPN 患者的突变景观和详细的 JAK2V617F 克隆结构有了更广泛的了解。

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