Vasudev Naveen S, Reynolds Andrew R
Tumour Biology Team, Breakthrough Breast Cancer Research Centre, The Institute of Cancer Research, Fulham Road, London, SW3 6JB, UK.
Angiogenesis. 2014 Jul;17(3):471-94. doi: 10.1007/s10456-014-9420-y. Epub 2014 Jan 31.
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.
肿瘤生长需要血管供应,可通过表达促血管生成生长因子来实现这一点,这些因子包括血管内皮生长因子(VEGF)配体家族的成员。由于VEGF配体家族中的一种或多种在大多数实体癌中过度表达,人们曾非常乐观地认为抑制VEGF通路将成为针对大多数肿瘤类型的有效抗血管生成疗法。令人鼓舞的是,贝伐单抗、舒尼替尼和阿柏西普等靶向VEGF通路的药物在某些情况下已显示出活性。然而,抑制VEGF信号传导在所有癌症中并不都有效,这促使人们需要进一步了解如何在肿瘤中有效地靶向脉管系统。在此,我们简要综述VEGF靶向治疗的进展以及该领域存在的未解决问题:包括其在不同疾病阶段(转移性、辅助性、新辅助性)的应用、与化疗的相互作用、治疗持续时间和疗程安排、潜在的预测性生物标志物以及提出的耐药机制,包括诸如增强肿瘤侵袭性等矛盾效应。在未来方向方面,我们讨论了如果要开发更有效和个性化的抗血管生成疗法,需要进一步阐明肿瘤血管生成的复杂性。