Vascular endothelial growth factor receptors and the therapeutic targeting of angiogenesis in cancer: where do we go from here?

Q2 Biochemistry, Genetics and Molecular Biology
Cell Communication and Adhesion Pub Date : 2011-10-01 Epub Date: 2011-10-24 DOI:10.3109/15419061.2011.619673
David Bruce, Peng H Tan
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引用次数: 24

Abstract

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.

血管内皮生长因子受体和肿瘤血管生成的治疗靶点:我们将何去何从?
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,一些疗法已成功推向市场。目前,VEGFR抑制剂似乎是最有希望作为常规化疗佐剂的药物。然而,一些相互作用的信号分子和下游途径最近被证明与VEGFR信号相互作用,并提供了有希望的新靶点,如血小板衍生生长因子(PDGF),上皮生长因子(EGF),人上皮受体-2,(HER-2) -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,这些策略可能与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,并系统地检查了该领域的现有证据和试验。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Cell Communication and Adhesion
Cell Communication and Adhesion 生物-生化与分子生物学
CiteScore
2.50
自引率
0.00%
发文量
0
审稿时长
>12 weeks
期刊介绍: Cessation Cell Communication and Adhesion is an international Open Access journal which provides a central forum for research on mechanisms underlying cellular signalling and adhesion. The journal provides a single source of information concerning all forms of cellular communication, cell junctions, adhesion molecules and families of receptors from diverse biological systems. The journal welcomes submission of original research articles, reviews, short communications and conference reports.
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