骨髓纤维化
间充质干细胞
骨髓增生性肿瘤
干细胞
医学
造血
骨髓
骨髓增生性疾病
造血干细胞
癌症研究
间质细胞
免疫学
髓外造血
病理
生物
细胞生物学
作者
Sonia Selicean,Ciprian Tomuleasa,Ravnit Grewal,Graça Almeida‐Porada,Ioana Berindan‐Neagoe
标识
DOI:10.1080/10428194.2018.1516881
摘要
Primary myelofibrosis (PMF) is the most aggressive Philadelphia-negative (Ph-) myeloproliferative neoplasm (MPN), characterized by bone marrow (BM) insufficiency, myelofibrosis (MF), osteosclerosis, neoangiogenesis, and extramedullary hematopoiesis (EMH) in spleen and liver. Presently, there is no curative treatment for this disease and therapy consists primarily of symptom relief and, in selected cases, allogeneic hematopoietic stem cell transplant (alloHSCT). PMF's major defining characteristics, as well as several recently described aspects of its cellular and molecular pathophysiology all support a critical role for dysregulated cell-cell/cell-extracellular matrix interactions and cytokine/chemokine signaling within the BM niche in the natural history of this disease. This review will highlight current data concerning the involvement of the BM niche, particularly of mesenchymal stem cells (MSC), in PMF, and will then discuss the rationale for a stroma-directed treatment, and the advantages such an approach would offer over the current treatments focused on targeting the malignant clone.
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