Rajabi Mehdi, Mousa Shaker A
Pharmaceutical Research Institute, Albany College of Pharmacy and Health Sciences, Rensselaer, NY 12144, USA.
Biomedicines. 2017 Jun 21;5(2):34. doi: 10.3390/biomedicines5020034.
A number of anti-angiogenesis drugs have been FDA-approved and are being used in cancer treatment, and a number of other agents are in different stages of clinical development or in preclinical evaluation. However, pharmacologic anti-angiogenesis strategies that arrest tumor progression might not be enough to eradicate tumors. Decreased anti-angiogenesis activity in single mechanism-based anti-angiogenic strategies is due to the redundancy, multiplicity, and development of compensatory mechanism by which blood vessels are remodeled. Improving anti-angiogenesis drug efficacy will require identification of broad-spectrum anti-angiogenesis targets. These strategies may have novel features, such as increased porosity, and are the result of complex interactions among endothelial cells, extracellular matrix proteins, growth factors, pericyte, and smooth muscle cells. Thus, combinations of anti-angiogenic drugs and other anticancer strategies such as chemotherapy appear essential for optimal outcome in cancer patients. This review will focus on the role of anti-angiogenesis strategies in cancer treatment.
多种抗血管生成药物已获美国食品药品监督管理局(FDA)批准并用于癌症治疗,还有多种其他药物正处于临床开发的不同阶段或临床前评估阶段。然而,阻止肿瘤进展的药理学抗血管生成策略可能不足以根除肿瘤。基于单一机制的抗血管生成策略中抗血管生成活性降低是由于血管重塑的冗余性、多样性以及代偿机制的发展。提高抗血管生成药物疗效将需要识别广谱抗血管生成靶点。这些策略可能具有诸如孔隙率增加等新特性,并且是内皮细胞、细胞外基质蛋白、生长因子、周细胞和平滑肌细胞之间复杂相互作用的结果。因此,抗血管生成药物与其他抗癌策略(如化疗)联合使用对于癌症患者获得最佳治疗效果似乎至关重要。本综述将聚焦于抗血管生成策略在癌症治疗中的作用。