Department of Anatomy and Cell Biology, University of Florida, Gainesville, FL 32610, USA.
Front Biosci (Landmark Ed). 2011 Jan 1;16(3):803-14. doi: 10.2741/3721.
Despite advances in surgery, radiation therapy, and chemotherapy, patients with cancer have a poor prognosis. Sustained aberrant tumor angiogenesis and metastasis is a major obstacle for effective cancer treatment. Just a few years ago, few would argue that one of the key success stories of the modern cancer medicine were the anti-angiogenic drugs targeting the vascular endothelial growth factor (VEGF) signaling pathway approved by FDA. This initial success inspired many researchers to search for new anti-angiogenic targets and drugs with the hope that one day, anti-angiogenic therapy might really become the panacea for cancer patients. Unfortunately, the limited clinical benefits achieved with anti-angiogenic drugs conflicts with the widely accepted notion that angiogenesis is a key event in tumor progression. Emerging data indicate that unique characteristics of the tumor vasculature within the tumor microenvironment may hold the key for success of anti-angiogenic therapy. In particular, the molecular and cellular alterations that sustain aberrant tumor angiogenesis in the face of angiogenic inhibitors represents novel targets for rationally designing and improving current anti-angiogenic strategies.
尽管手术、放疗和化疗方面取得了进展,但癌症患者的预后仍然很差。肿瘤血管生成和转移的持续异常是癌症治疗的主要障碍。就在几年前,很少有人会争辩说,FDA 批准的针对血管内皮生长因子 (VEGF) 信号通路的抗血管生成药物是现代癌症医学的主要成功案例之一。这一初步成功激发了许多研究人员寻找新的抗血管生成靶点和药物,希望有一天,抗血管生成疗法真的能成为癌症患者的万能药。不幸的是,抗血管生成药物所取得的有限临床获益与广泛接受的观点相冲突,即血管生成是肿瘤进展的关键事件。新出现的数据表明,肿瘤微环境中肿瘤血管的独特特征可能是抗血管生成治疗成功的关键。特别是,在抗血管生成抑制剂的情况下维持异常肿瘤血管生成的分子和细胞改变为合理设计和改进当前抗血管生成策略提供了新的靶点。