首页> 美国卫生研究院文献>Springer Open Choice >Anti-angiogenic therapy for cancer: current progress unresolved questions and future directions
【2h】

Anti-angiogenic therapy for cancer: current progress unresolved questions and future directions

机译:癌症抗血管生成疗法:当前进展未解决的问题和未来方向

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Tumours require a vascular supply to grow and can achieve this via the expression of pro-angiogenic growth factors, including members of the vascular endothelial growth factor (VEGF) family of ligands. Since one or more of the VEGF ligand family is overexpressed in most solid cancers, there was great optimism that inhibition of the VEGF pathway would represent an effective anti-angiogenic therapy for most tumour types. Encouragingly, VEGF pathway targeted drugs such as bevacizumab, sunitinib and aflibercept have shown activity in certain settings. However, inhibition of VEGF signalling is not effective in all cancers, prompting the need to further understand how the vasculature can be effectively targeted in tumours. Here we present a succinct review of the progress with VEGF-targeted therapy and the unresolved questions that exist in the field: including its use in different disease stages (metastatic, adjuvant, neoadjuvant), interactions with chemotherapy, duration and scheduling of therapy, potential predictive biomarkers and proposed mechanisms of resistance, including paradoxical effects such as enhanced tumour aggressiveness. In terms of future directions, we discuss the need to delineate further the complexities of tumour vascularisation if we are to develop more effective and personalised anti-angiogenic therapies.
机译:肿瘤需要血管供应才能生长,并且可以通过表达促血管生成生长因子来实现,其中包括血管内皮生长因子(VEGF)配体家族的成员。由于一种或多种VEGF配体家族在大多数实体癌中均过表达,因此人们非常乐观地认为,抑制VEGF途径可代表大多数肿瘤类型的有效抗血管生成疗法。令人鼓舞的是,靶向VEGF途径的药物(例如贝伐单抗,舒尼替尼和阿柏西普)在某些情况下显示出活性。但是,VEGF信号传导的抑制并非在所有癌症中都有效,因此需要进一步了解如何有效地靶向肿瘤中的脉管系统。在这里,我们简要概述了VEGF靶向疗法的进展以及该领域中尚未解决的问题:包括其在不同疾病阶段的使用(转移性,辅助性,新辅助性),与化疗的相互作用,治疗的持续时间和时间表,潜在的预测性生物标志物和拟议的耐药机制,包括反常效应,例如增强的肿瘤侵袭性。在未来的方向上,我们讨论了如果我们要开发更有效和个性化的抗血管生成疗法,则需要进一步描述肿瘤血管形成的复杂性。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号