Department I of Internal Medicine, University of Cologne, Cologne, Germany.
Manitoba Institute of Cell Biology, University of Manitoba, Winnipeg, MB, Canada.
Crit Rev Oncol Hematol. 2015 Mar;93(3):225-36. doi: 10.1016/j.critrevonc.2014.10.007. Epub 2014 Oct 12.
The role of angiogenesis in haematological malignancies such as chronic lymphocytic leukaemia (CLL) is difficult to envision, because leukaemia cells are not dependent on a network of blood vessels to support basic physiological requirements. Regardless, CLL cells secrete high levels of major angiogenic factors, such as vascular endothelial growth factor (VEGF), basic fibroblast growth factor (bFGF), and platelet derived growth factor (PDGF). Nonetheless, it remains unclear how most angiogenic factors regulate accumulation and delayed apoptosis of CLL cells. Angiogenic factors such as leptin, granulocyte colony-stimulating factor (G-CSF), follistatin, angiopoietin-1 (Ang1), angiogenin (ANG), midkine (MK), pleiotrophin (PTN), progranulin (PGRN), proliferin (PLF), placental growth factor (PIGF), and endothelial locus-1 (Del-1), represent novel therapeutic targets of future CLL research but have remained widely overlooked. This review aims to outline our current understanding of angiogenic growth factors and their relationship with CLL, a still uncured haematopoietic malignancy.
血管生成在血液系统恶性肿瘤(如慢性淋巴细胞白血病(CLL))中的作用难以想象,因为白血病细胞不依赖血管网络来支持基本的生理需求。尽管如此,CLL 细胞仍会分泌高水平的主要血管生成因子,如血管内皮生长因子(VEGF)、碱性成纤维细胞生长因子(bFGF)和血小板衍生生长因子(PDGF)。然而,大多数血管生成因子如何调节 CLL 细胞的积累和延迟凋亡仍不清楚。瘦素、粒细胞集落刺激因子(G-CSF)、卵泡抑素、血管生成素-1(Ang1)、血管生成素(ANG)、中期因子(MK)、多效蛋白(PTN)、颗粒蛋白前体(PGRN)、增殖蛋白(PLF)、胎盘生长因子(PIGF)和内皮基因座-1(Del-1)等血管生成因子是未来 CLL 研究的新治疗靶点,但仍被广泛忽视。本综述旨在概述我们目前对血管生成生长因子及其与 CLL 的关系的理解,CLL 是一种尚未治愈的造血恶性肿瘤。