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JAK2 V617F突变对PRV-1表达的影响。

The effect of the JAK2 V617F mutation on PRV-1 expression.

作者信息

Mnjoyan Zakar, Yoon Donghoon, Li Jun, Delhommeau François, Afshar-Kharghan Vahid

出版信息

Haematologica. 2006 Mar;91(3):411-2. Epub 2006 Feb 17.

PMID:16503546
Abstract

JAK2(V617F)an acquired mutation of JAK2, is present in a majority of patients with polycythemia vera and to a lesser extent among patients with the other myeloproliferative disorders. We analyzed the effect of JAK2(V617F) on the expression of polycythemia rubra vera 1(PRV-1), using an in vitro model. Compared to wild-type JAK2, the presence of JAK2(V617F) increased both PRV-1 protein and mRNA levels in murine myeloid cells. A JAK2 inhibitor eliminated the V617F-induced increase in PRV-1 expression.

摘要

JAK2(V617F)是JAK2的一种获得性突变,存在于大多数真性红细胞增多症患者中,在其他骨髓增殖性疾病患者中出现的比例较低。我们使用体外模型分析了JAK2(V617F)对真性红细胞增多症1(PRV-1)表达的影响。与野生型JAK2相比,JAK2(V617F)的存在增加了小鼠骨髓细胞中PRV-1蛋白和mRNA水平。一种JAK2抑制剂消除了V617F诱导的PRV-1表达增加。

相似文献

1
The effect of the JAK2 V617F mutation on PRV-1 expression.JAK2 V617F突变对PRV-1表达的影响。
Haematologica. 2006 Mar;91(3):411-2. Epub 2006 Feb 17.
2
Concomitant neutrophil JAK2 mutation screening and PRV-1 expression analysis in myeloproliferative disorders and secondary polycythaemia.骨髓增殖性疾病和继发性红细胞增多症中中性粒细胞JAK2突变筛查与PRV-1表达分析的同步进行
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JAK2 V617F mutation, PRV-1 overexpression and endogenous erythroid colony formation show different coexpression patterns among Ph-negative chronic myeloproliferative disorders.JAK2 V617F突变、PRV-1过表达和内源性红系集落形成在Ph阴性慢性骨髓增殖性疾病中呈现不同的共表达模式。
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Application of PRV-1 mRNA expression level and JAK2V617F mutation for the differentiating between polycytemia vera and secondary erythrocytosis and assessment of treatment by interferon or hydroxyurea.PRV-1 mRNA表达水平和JAK2V617F突变在真性红细胞增多症与继发性红细胞增多症鉴别诊断及干扰素或羟基脲治疗评估中的应用
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Inconsistencies in the association between the JAK2(V617F) mutation and PRV-1 over-expression among the chronic myeloproliferative diseases.慢性骨髓增殖性疾病中JAK2(V617F)突变与PRV-1过表达之间关联的不一致性。
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引用本文的文献

1
Deregulation of apoptosis-related genes is associated with PRV1 overexpression and JAK2 V617F allele burden in Essential Thrombocythemia and Myelofibrosis.凋亡相关基因的失调与原发性血小板增多症和骨髓纤维化中 PRV1 过表达和 JAK2 V617F 等位基因负担有关。
J Hematol Oncol. 2012 Feb 2;5:2. doi: 10.1186/1756-8722-5-2.