Lenz Heinz-Josef
USC/Norris Comprehensive Cancer Center, USC Keck School of Medicine, Los Angeles, California 90033, USA.
Oncology (Williston Park). 2005 Apr;19(4 Suppl 3):17-25.
There is substantial preclinical and clinical evidence that angiogenesis plays a role in the development of tumors and the progression of malignancies. Inhibiting angiogenesis has been shown to suppress tumor growth and metastasis in many preclinical models. These benefits have translated to the clinic with both marketed and investigational antiangiogenesis agents. The most prominent target of these compounds is vascular endothelial growth factor (VEGF) and its receptors. However, several other factors are of interest as well. These include integrins, matrix metalloproteinases, and endogenous antiangiogenic factors. Data from late-stage clinical trials support the role of antiangiogenic agents in cancer therapy and the significant role that VEGF plays in angiogenesis. Future research will focus on determining the tumor types and stages that will benefit most from antiangiogenic therapy and combining therapies that target different factors in the angiogenesis pathway.
有大量临床前和临床证据表明血管生成在肿瘤发展和恶性肿瘤进展中起作用。在许多临床前模型中,抑制血管生成已被证明可抑制肿瘤生长和转移。这些益处已通过已上市和正在研究的抗血管生成药物转化到临床。这些化合物最主要的靶点是血管内皮生长因子(VEGF)及其受体。然而,其他几个因素也受到关注。这些因素包括整合素、基质金属蛋白酶和内源性抗血管生成因子。晚期临床试验的数据支持抗血管生成药物在癌症治疗中的作用以及VEGF在血管生成中所起的重要作用。未来的研究将集中于确定最能从抗血管生成治疗中获益的肿瘤类型和阶段,以及联合针对血管生成途径中不同因素的治疗方法。