James Chloé, Ugo Valérie, Le Couédic Jean-Pierre, Staerk Judith, Delhommeau François, Lacout Catherine, Garçon Loïc, Raslova Hana, Berger Roland, Bennaceur-Griscelli Annelise, Villeval Jean Luc, Constantinescu Stefan N, Casadevall Nicole, Vainchenker William
INSERM U362, Institut Gustave Roussy, Paris XI University, PR1, 39 rue Camille Desmoulins, 94805 Villejuif Cedex, France.
Nature. 2005 Apr 28;434(7037):1144-8. doi: 10.1038/nature03546.
Myeloproliferative disorders are clonal haematopoietic stem cell malignancies characterized by independency or hypersensitivity of haematopoietic progenitors to numerous cytokines. The molecular basis of most myeloproliferative disorders is unknown. On the basis of the model of chronic myeloid leukaemia, it is expected that a constitutive tyrosine kinase activity could be at the origin of these diseases. Polycythaemia vera is an acquired myeloproliferative disorder, characterized by the presence of polycythaemia diversely associated with thrombocytosis, leukocytosis and splenomegaly. Polycythaemia vera progenitors are hypersensitive to erythropoietin and other cytokines. Here, we describe a clonal and recurrent mutation in the JH2 pseudo-kinase domain of the Janus kinase 2 (JAK2) gene in most (> 80%) polycythaemia vera patients. The mutation, a valine-to-phenylalanine substitution at amino acid position 617, leads to constitutive tyrosine phosphorylation activity that promotes cytokine hypersensitivity and induces erythrocytosis in a mouse model. As this mutation is also found in other myeloproliferative disorders, this unique mutation will permit a new molecular classification of these disorders and novel therapeutical approaches.
骨髓增殖性疾病是克隆性造血干细胞恶性肿瘤,其特征是造血祖细胞对多种细胞因子具有自主性或超敏性。大多数骨髓增殖性疾病的分子基础尚不清楚。基于慢性髓性白血病的模型,预计组成型酪氨酸激酶活性可能是这些疾病的起源。真性红细胞增多症是一种获得性骨髓增殖性疾病,其特征是存在真性红细胞增多症,并伴有不同程度的血小板增多、白细胞增多和脾肿大。真性红细胞增多症祖细胞对促红细胞生成素和其他细胞因子超敏。在此,我们描述了大多数(>80%)真性红细胞增多症患者中Janus激酶2(JAK2)基因的JH2假激酶结构域存在克隆性和复发性突变。该突变是氨基酸位置617处的缬氨酸到苯丙氨酸取代,导致组成型酪氨酸磷酸化活性,促进细胞因子超敏反应,并在小鼠模型中诱导红细胞增多症。由于该突变也存在于其他骨髓增殖性疾病中,这种独特的突变将允许对这些疾病进行新的分子分类和新的治疗方法。