Margolin Kim
Departments of Medical Oncology and Therapeutics Research, City of Hope National Medical Center, 1500 East Duarte Road, Duarte, CA 91010, USA.
Curr Oncol Rep. 2002 Jan;4(1):20-8. doi: 10.1007/s11912-002-0044-9.
Vascular endothelial growth factor (VEGF) is the term used for a family of tumor-derived angiogenic factors that mediate endothelial proliferation and vascular permeability. Preclinical models have demonstrated the essential nature of VEGF in the angiogenesis of solid tumor growth and metastasis, whereas pathologic investigations have revealed strong correlations between VEGF production, microvessel density, and overall aggressiveness of many human solid tumors. Recent advances in the understanding of the molecular mechanisms of VEGF action have led to successful models for intervention in VEGF-mediated pathways in therapy for solid tumors. These include antibodies to block the binding of VEGF to its cellular receptors, small-molecule chemical inhibitors of the tyrosine kinase functions of the VEGF receptors, and antisense nucleic acids to interfere with cellular production of VEGF. Clinical investigations are ongoing to test the value of VEGF-based intervention alone or in combination with other anticancer agents.
血管内皮生长因子(VEGF)是用于称呼一族肿瘤源性血管生成因子的术语,这些因子介导内皮细胞增殖和血管通透性。临床前模型已证明VEGF在实体瘤生长和转移的血管生成中具有本质性作用,而病理学研究则揭示了VEGF产生、微血管密度与许多人类实体瘤的总体侵袭性之间存在密切关联。对VEGF作用分子机制认识的最新进展已促成了在实体瘤治疗中干预VEGF介导途径的成功模型。这些模型包括阻断VEGF与其细胞受体结合的抗体、VEGF受体酪氨酸激酶功能的小分子化学抑制剂以及干扰细胞产生VEGF的反义核酸。目前正在进行临床研究以测试基于VEGF的干预单独使用或与其他抗癌药物联合使用的价值。