Maj Ewa, Papiernik Diana, Wietrzyk Joanna
Hirszfeld Institute of Immunology and Experimental Therapy, Polish Academy of Sciences, 53-114 Wroclaw, Poland.
Int J Oncol. 2016 Nov;49(5):1773-1784. doi: 10.3892/ijo.2016.3709. Epub 2016 Sep 26.
The discovery of tumor angiogenesis opened a new path in fighting cancer. The approval of different antiangiogenic agents, most targeting vascular endothelial growth factor (VEGF) signaling, has either increased the effectiveness of standard chemotherapy or even replaced it by offering better patient outcomes. However, an increasing number of preclinical and clinical observations have shown that the process of angiogenesis is far from clearly understood. Apart from targeting the VEGF pathway, novel strategies aim to influence other molecular factors that are involved in tumor angiogenesis. In addition, naturally occurring compounds seem to offer additional agents for influencing angiogenesis. The first concept of antiangiogenic therapy aimed to destroy tumor vessels, while it turned out that, paradoxically, antiangiogenic drugs normalized vasculature and as a result offered an improvement in chemotherapeutic delivery. In order to design an effective treatment schedule, methods for detecting the time window of normalization and biomarkers predicting patient response are needed. The initial idea that antiangiogenic therapy would be resistance-free failed to materialize and currently we still face the obstacle of resistance to antiangiogenic therapy.
肿瘤血管生成的发现为抗击癌症开辟了一条新途径。不同抗血管生成药物的获批,其中大多数靶向血管内皮生长因子(VEGF)信号通路,要么提高了标准化疗的疗效,要么通过提供更好的患者预后甚至取代了标准化疗。然而,越来越多的临床前和临床观察表明,血管生成过程远未被清楚理解。除了靶向VEGF通路外,新策略旨在影响参与肿瘤血管生成的其他分子因子。此外,天然存在的化合物似乎为影响血管生成提供了额外的药物。抗血管生成治疗的最初概念旨在破坏肿瘤血管,而事实证明,矛盾的是,抗血管生成药物使血管系统正常化,结果改善了化疗药物的递送。为了设计有效的治疗方案,需要检测正常化时间窗的方法和预测患者反应的生物标志物。抗血管生成治疗无耐药性的最初想法未能实现,目前我们仍然面临抗血管生成治疗耐药性的障碍。