Department of Dermatology, University Hospital Essen, Hufelandstrasse 55, D-45122 Essen, Germany.
Mol Oncol. 2011 Apr;5(2):137-49. doi: 10.1016/j.molonc.2011.01.003. Epub 2011 Feb 3.
Angiogenesis is a pivotal process for growth, invasion and spread of the majority of solid tumors including melanoma. Anti-angiogenic agents have not been systematically tested in patients with advanced melanoma. Clinical efficacy of angiogenesis inhibitors targeting endothelial cells has not been as affirmative as initially hoped and improved clinical outcomes have been observed in combination with chemotherapy or additional drugs for many types of human cancer. However, angiogenesis is not only dependent on endothelial cell invasion and proliferation, it also requires pericyte coverage of vascular sprouts for stabilization and maturation of vascular walls. Recent data suggest that pericytes might be able to confer resistance to anti-vascular endothelial growth factor (VEGF) therapy. This review will focus on the significance of the vascular phenotype but also on the impact of pericyte-mediated vessel maturation for the susceptibility to anti-angiogenic therapy, including malignant melanoma, which we identified as crucial factor regarding therapeutic efficacy.
血管生成是大多数实体瘤(包括黑色素瘤)生长、侵袭和扩散的关键过程。抗血管生成药物尚未在晚期黑色素瘤患者中进行系统测试。针对内皮细胞的血管生成抑制剂的临床疗效并不像最初预期的那样肯定,并且在许多类型的人类癌症中与化疗或其他药物联合使用时观察到了改善的临床结果。然而,血管生成不仅依赖于内皮细胞的侵袭和增殖,还需要周细胞覆盖血管芽,以稳定和成熟血管壁。最近的数据表明,周细胞可能能够赋予对抗血管内皮生长因子(VEGF)治疗的耐药性。这篇综述将重点关注血管表型的意义,以及周细胞介导的血管成熟对血管生成治疗敏感性的影响,包括恶性黑色素瘤,我们认为这是治疗效果的关键因素。