Kanda Shigeru, Miyata Yasuyoshi, Kanetake Hiroshi
Department of Molecular Microbiology and Immunology, Division of Endothelial Cell Biology, Nagasaki University Graduate School of Biomedical Science, 1-7-1 Sakamoto, Nagasaki 852-8501, Japan.
Int J Clin Oncol. 2006 Apr;11(2):90-107. doi: 10.1007/s10147-006-0565-6.
Angiogenesis is considered a prerequisite for solid tumor growth. Antiangiogenic therapy reduces tumor size and extends host survival in a number of preclinical animal models. However, in humans antiangiogenic therapy is a poor promoter of tumor regression and has shown minimal effect on patient survival. In urinary cancers, such as renal cell cancer, prostate cancer, and bladder cancer, advanced refractory disease is a good candidate for antiangiogenic therapy because of its resistance to ordinary chemotherapy, radiotherapy, and hormonal therapy. Unique characteristics of molecular mechanisms underlie the induction of angiogenesis in urinary cancers. In this review, we summarize these unique mechanisms and review the results of clinical trials of antiangiogenic therapy for these cancers, discussing prospects and problems relating to antiangiogenic therapy.
血管生成被认为是实体瘤生长的先决条件。在许多临床前动物模型中,抗血管生成疗法可减小肿瘤大小并延长宿主生存期。然而,在人类中,抗血管生成疗法对肿瘤消退的促进作用不佳,对患者生存期的影响也微乎其微。在泌尿系统癌症,如肾细胞癌、前列腺癌和膀胱癌中,晚期难治性疾病是抗血管生成疗法的理想候选对象,因为它对普通化疗、放疗和激素疗法具有抗性。泌尿系统癌症中血管生成诱导的分子机制具有独特特征。在本综述中,我们总结了这些独特机制,并回顾了这些癌症抗血管生成疗法的临床试验结果,讨论了与抗血管生成疗法相关的前景和问题。