Medinger Michael, Passweg Jakob
Haematology, University Hospital Basel, Switzerland.
Swiss Med Wkly. 2014 Nov 6;144:w14050. doi: 10.4414/smw.2014.14050. eCollection 2014.
Tumour angiogenesis plays a key role in the pathogenesis and progression of haematological malignancies. Thereby, pro- and anti-angiogenic growth factors and cytokines regulate the angiogenic process. The most important growth factor, vascular endothelial growth factor (VEGF) and its signaling through its receptors 1 and 2, is not only involved in solid tumours, but there is also emerging evidence that tumour progression in haematological malignancies also depends on the induction of new blood vessel formation. The evidence supporting this theory includes the finding of increased bone marrow microvessel density and increased levels of plasma pro-angiogenic cytokines. Leukaemia cells interact with surrounding host cells and extracellular matrix, this crosstalk affecting the most important aspects of the malignant phenotype. The pathophysiology of leukaemia induced angiogenesis involves both direct production of angiogenic cytokines by leukaemia cells and their interaction with bone marrow microenvironment. The inhibition of VEGF signalling by monoclonal antibodies or small molecules (kinase inhibitors) has already been successfully used for the treatment of different cancer entities, and multiple new drugs are being tested. This review summarises recent advances in the basic understanding of the role of angiogenesis in haematological malignancies and the translation of such basic findings into clinical studies.
肿瘤血管生成在血液系统恶性肿瘤的发病机制和进展中起着关键作用。因此,促血管生成和抗血管生成生长因子及细胞因子调节血管生成过程。最重要的生长因子——血管内皮生长因子(VEGF)及其通过受体1和2的信号传导,不仅参与实体瘤,而且越来越多的证据表明血液系统恶性肿瘤的进展也依赖于新血管形成的诱导。支持这一理论的证据包括骨髓微血管密度增加和血浆促血管生成细胞因子水平升高。白血病细胞与周围宿主细胞及细胞外基质相互作用,这种相互作用影响恶性表型的最重要方面。白血病诱导血管生成的病理生理学涉及白血病细胞直接产生血管生成细胞因子及其与骨髓微环境的相互作用。单克隆抗体或小分子(激酶抑制剂)对VEGF信号的抑制已成功用于治疗不同的癌症实体,并且多种新药正在进行测试。本综述总结了对血管生成在血液系统恶性肿瘤中的作用的基本认识以及将这些基本发现转化为临床研究的最新进展。