Yung Yammy, Lee Emily, Chu Hiu-Tung, Yip Pui-Kwan, Gill Harinder
Division of Haematology, Medical Oncology and Haemopoietic Stem Cell transplantation, Department of Medicine, LKS Faculty of Medicine, The University of Hong Kong, Hong Kong, China.
Int J Mol Sci. 2021 Jan 11;22(2):659. doi: 10.3390/ijms22020659.
Myeloproliferative neoplasms (MPNs) are unique hematopoietic stem cell disorders sharing mutations that constitutively activate the signal-transduction pathways involved in haematopoiesis. They are characterized by stem cell-derived clonal myeloproliferation. The key MPNs comprise chronic myeloid leukemia (CML), polycythemia vera (PV), essential thrombocythemia (ET), and primary myelofibrosis (PMF). CML is defined by the presence of the Philadelphia (Ph) chromosome and fusion gene. Despite effective cytoreductive agents and targeted therapy, complete CML/MPN stem cell eradication is rarely achieved. In this review article, we discuss the novel agents and combination therapy that can potentially abnormal hematopoietic stem cells in CML and MPNs and the CML/MPN stem cell-sustaining bone marrow microenvironment.
骨髓增殖性肿瘤(MPNs)是一类独特的造血干细胞疾病,具有共同的突变,这些突变可组成性激活参与造血的信号转导通路。它们的特征是干细胞来源的克隆性骨髓增殖。主要的MPNs包括慢性髓性白血病(CML)、真性红细胞增多症(PV)、原发性血小板增多症(ET)和原发性骨髓纤维化(PMF)。CML由费城(Ph)染色体和融合基因的存在所定义。尽管有有效的细胞减灭剂和靶向治疗,但很少能实现完全清除CML/MPN干细胞。在这篇综述文章中,我们讨论了可能作用于CML和MPNs中异常造血干细胞以及维持CML/MPN干细胞的骨髓微环境的新型药物和联合疗法。