Yang Qiong, Crispino John D, Wen Qiang Jeremy
Beijing Key Laboratory of Gene Resource and Molecular Development, College of Life Sciences, Beijing Normal University, Beijing, China.
Division of Hematology and Oncology, Department of Medicine, Northwestern University, Chicago, IL.
Exp Hematol. 2017 Apr;48:32-38. doi: 10.1016/j.exphem.2016.12.007. Epub 2016 Dec 30.
The myeloproliferative neoplasms (MPNs) are somatic mutation-driven hematologic malignancies characterized by bone marrow fibrosis and the accumulation of atypical megakaryocytes with reduced polyploidization in the primary myelofibrosis subtype of the MPNs. Increasing evidence points to a dominant role of abnormal megakaryocytes in disease initiation and progression. Here we review the literature related to kinase signaling pathways relevant to megakaryocyte differentiation and proliferation, including Aurora A kinase, RhoA/ROCK, and JAK/STAT, as well as the activities of their targeted inhibitors in models of the disease. Some of these pathway inhibitors selectively induce megakaryocyte differentiation, suppress malignant proliferation, and promote polyploidization and proplatelet formation. Moreover, combining sets of these inhibitors may be an effective approach to treat and potentially cure MPN patients. For example, preclinical studies reported significant synergistic effects of the combination of an Aurora A inhibitor and JAK1/2 inhibitor, in a murine model of the primary myelofibrosis. Future basic and clinical research into the contributions of these signaling pathways to aberrant megakaryopoiesis may lead to novel effective treatments for MPN patients.
骨髓增殖性肿瘤(MPN)是由体细胞突变驱动的血液系统恶性肿瘤,其特征为骨髓纤维化以及在MPN的原发性骨髓纤维化亚型中存在非典型巨核细胞积聚且多倍体化减少。越来越多的证据表明异常巨核细胞在疾病的起始和进展中起主导作用。在此,我们综述了与巨核细胞分化和增殖相关的激酶信号通路的文献,包括极光激酶A、RhoA/ROCK和JAK/STAT,以及它们的靶向抑制剂在该疾病模型中的活性。其中一些通路抑制剂可选择性诱导巨核细胞分化、抑制恶性增殖并促进多倍体化和前血小板形成。此外,联合使用这些抑制剂可能是治疗并潜在治愈MPN患者的有效方法。例如,临床前研究报道,在原发性骨髓纤维化的小鼠模型中,极光激酶A抑制剂和JAK1/2抑制剂联合使用具有显著的协同效应。未来对这些信号通路在异常巨核细胞生成中的作用进行的基础和临床研究,可能会为MPN患者带来新的有效治疗方法。