Liongue Clifford, Ward Alister C
School of Medicine, Deakin University, Waurn Ponds, VIC 3216, Australia.
Institute for Mental and Physical Health and Clinical Translation, Deakin University, Waurn Ponds, VIC 3216, Australia.
Cancers (Basel). 2024 Jan 11;16(2):313. doi: 10.3390/cancers16020313.
Myeloproliferative neoplasms (MPNs) are hematopoietic diseases characterized by the clonal expansion of single or multiple lineages of differentiated myeloid cells that accumulate in the blood and bone marrow. MPNs are grouped into distinct categories based on key clinical presentations and distinctive mutational hallmarks. These include chronic myeloid leukemia (CML), which is strongly associated with the signature gene translocation, polycythemia vera (PV), essential thrombocythemia (ET), and primary (idiopathic) myelofibrosis (PMF), typically accompanied by molecular alterations in the , , or genes. There are also rarer forms such as chronic neutrophilic leukemia (CNL), which involves mutations in the gene. However, rather than focusing on the differences between these alternate disease categories, this review aims to present a unifying molecular etiology in which these overlapping diseases are best understood as disruptions of normal hematopoietic signaling: specifically, the chronic activation of signaling pathways, particularly involving signal transducer and activator of transcription (STAT) transcription factors, most notably STAT5B, leading to the sustained stimulation of myelopoiesis, which underpins the various disease sequalae.
骨髓增殖性肿瘤(MPNs)是一类造血系统疾病,其特征为分化的髓系细胞单系或多系的克隆性扩增,这些细胞在血液和骨髓中蓄积。MPNs根据关键临床表现和独特的突变特征分为不同类别。这些类别包括与标志性基因易位密切相关的慢性髓性白血病(CML)、真性红细胞增多症(PV)、原发性血小板增多症(ET)以及原发性(特发性)骨髓纤维化(PMF),后者通常伴有JAK2、CALR或MPL基因的分子改变。还有一些较为罕见的类型,如慢性中性粒细胞白血病(CNL),其涉及CSF3R基因的突变。然而,本综述并非聚焦于这些不同疾病类别的差异,而是旨在呈现一种统一的分子病因学,在这种病因学中,这些重叠性疾病最好被理解为正常造血信号传导的破坏:具体而言,是信号传导通路的慢性激活,特别是涉及信号转导和转录激活因子(STAT)转录因子,最显著的是STAT5B,导致骨髓生成的持续刺激,这是各种疾病后遗症的基础。