Vasudev, NS orcid.org/0000-0001-8470-7481 and Reynolds, AR (2014) Anti-angiogenic therapy for cancer: Current progress, unresolved questions and future directions. Angiogenesis, 17 (3). pp. 471-494. ISSN 0969-6970
Abstract
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. © 2014 The Author(s).
Metadata
Item Type: | Article |
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Authors/Creators: |
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Copyright, Publisher and Additional Information: | � The Author(s) 2014. This article is published with open access at Springerlink.com This article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited. |
Keywords: | VEGF; Angiogenesis; Metastasis; Resistance; Microenvironment; Personalised medicine |
Dates: |
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Institution: | The University of Leeds |
Depositing User: | Symplectic Publications |
Date Deposited: | 03 Jan 2017 15:51 |
Last Modified: | 03 Jan 2017 15:51 |
Published Version: | https://doi.org/10.1007/s10456-014-9420-y |
Status: | Published |
Publisher: | Springer |
Identification Number: | 10.1007/s10456-014-9420-y |
Open Archives Initiative ID (OAI ID): | oai:eprints.whiterose.ac.uk:110033 |