Bruce David, Tan Peng H
Nuffield Department of Surgical Science, Oxford University, The John Radcliffe, Headley Way, Oxford, UK.
Cell Commun Adhes. 2011 Oct;18(5):85-103. doi: 10.3109/15419061.2011.619673. Epub 2011 Oct 24.
Abstract Vascular Endothelial Growth Factor receptors (VEGFRs), the interactions with their ligands and the subsequent signalling pathways are known to play a vital role in tumour angiogenesis. Initial clinical trials of VEGFR inhibitors were disappointing but over the past decade some therapies have been successfully brought to market. At present, VEGFR inhibitors appear to be most promising as adjuvants to conventional chemotherapy. However, several interacting signalling molecules and downstream pathways have recently been shown to interact with VEGFR signalling and provide promising novel targets, such as the platelet-derived growth factor (PDGF), epithelial growth factor (EGF), human epithelial receptor-2, (HER-2) Tie-2 and oestrogen receptors. Elucidation of this web of signalling pathways may identify new therapeutic strategies which may be used in combination with VEGFR inhibitors to augment the efficacy of anti-angiogenic cancer treatments. This review assesses the role of modulating VEGFR activity in cancer and systematically examines current evidence and trials in this area.
摘要 血管内皮生长因子受体(VEGFRs)及其与配体的相互作用以及随后的信号通路在肿瘤血管生成中起着至关重要的作用。VEGFR抑制剂的初步临床试验令人失望,但在过去十年中,一些疗法已成功上市。目前,VEGFR抑制剂作为传统化疗的辅助药物似乎最有前景。然而,最近有研究表明,几种相互作用的信号分子和下游通路与VEGFR信号相互作用,并提供了有前景的新靶点,如血小板衍生生长因子(PDGF)、上皮生长因子(EGF)、人表皮受体-2(HER-2)、Tie-2和雌激素受体。阐明这一信号通路网络可能会确定新的治疗策略,这些策略可与VEGFR抑制剂联合使用,以增强抗血管生成癌症治疗的疗效。本综述评估了调节VEGFR活性在癌症中的作用,并系统地审查了该领域的现有证据和试验。