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Can the co-dependence of the immune system and angiogenesis facilitate pharmacological targeting of tumours?

Mortara, Lorenzo; Benest, Andrew V; Bates, David O; Noonan, Douglas M

Authors

Lorenzo Mortara

DAVID BATES David.Bates@nottingham.ac.uk
Professor of Oncology

Douglas M Noonan



Abstract

Tumours elicit a number of mechanisms to induce a reprogramming of innate and adaptive immune cells to their advantage, inducing a pro-angiogenic phenotype. Investigation of these events is now leading to the identification of specific myeloid and lymphoid cell-targeted therapies, as well as of unexplored off-target activities of clinically relevant chemotherapeutic and metabolic drugs. It is also leading to an enhanced understanding of the interplay between angiogenesis and the immune system, and the value of novel co-targeting approaches using both immunotherapy and anti-angiogenic therapy. Here, we review recently identified mechanisms and potential pharmacological approaches targeting the crosstalk between cancer cells and the host immune system, providing an overview on novel therapeutic opportunities linking immuno-oncology and anti-angiogenic therapy.

Journal Article Type Article
Acceptance Date Jun 6, 2017
Online Publication Date Jun 14, 2017
Publication Date 2017-08
Deposit Date Apr 19, 2020
Journal Current Opinion in Pharmacology
Print ISSN 1471-4892
Electronic ISSN 1471-4973
Publisher Elsevier
Peer Reviewed Peer Reviewed
Volume 35
Pages 66-74
DOI https://doi.org/10.1016/j.coph.2017.05.009
Public URL https://nottingham-repository.worktribe.com/output/2572142
Publisher URL https://www.sciencedirect.com/science/article/abs/pii/S1471489217300516
Additional Information This article is maintained by: Elsevier; Article Title: Can the co-dependence of the immune system and angiogenesis facilitate pharmacological targeting of tumours?; Journal Title: Current Opinion in Pharmacology; CrossRef DOI link to publisher maintained version: https://doi.org/10.1016/j.coph.2017.05.009; Content Type: article; Copyright: © 2017 Elsevier Ltd. All rights reserved.