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Immune consequences of anti-angiogenic therapyin renal cell carcinoma

Current therapies of renal cell carcinoma (RCC), a highly vascularised tumour, mostly rely on anti-angiogenic treatment options. These include tyrosine kinase inhibitors (TKIs) and anti-VEGF monoclonal antibodies. Although these strategies aim at restraining vascularisation to control tumour growth,...

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Detalles Bibliográficos
Autores principales: Brodaczewska, Klaudia K., Szczylik, Cezary, Kieda, Claudine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Termedia Publishing House 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5885083/
https://www.ncbi.nlm.nih.gov/pubmed/29628789
http://dx.doi.org/10.5114/wo.2018.73878
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author Brodaczewska, Klaudia K.
Szczylik, Cezary
Kieda, Claudine
author_facet Brodaczewska, Klaudia K.
Szczylik, Cezary
Kieda, Claudine
author_sort Brodaczewska, Klaudia K.
collection PubMed
description Current therapies of renal cell carcinoma (RCC), a highly vascularised tumour, mostly rely on anti-angiogenic treatment options. These include tyrosine kinase inhibitors (TKIs) and anti-VEGF monoclonal antibodies. Although these strategies aim at restraining vascularisation to control tumour growth, the effects of such therapies are much wider, as affecting the vessel structure deeply modifies the microenvironment of the tumour mass. The aim of this review is to provide an overview of current knowledge on the global effects of anti-angiogenic treatment, mostly TKIs, on the shaping of the immune component of the RCC microenvironment. The data supporting the modification of immunity by anti-angiogenic therapies are collected to reveal the potential of angiogenesis modulation as a strategy for the adjuvant anti-cancer approach in immunotherapy.
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spelling pubmed-58850832018-04-06 Immune consequences of anti-angiogenic therapyin renal cell carcinoma Brodaczewska, Klaudia K. Szczylik, Cezary Kieda, Claudine Contemp Oncol (Pozn) Review Current therapies of renal cell carcinoma (RCC), a highly vascularised tumour, mostly rely on anti-angiogenic treatment options. These include tyrosine kinase inhibitors (TKIs) and anti-VEGF monoclonal antibodies. Although these strategies aim at restraining vascularisation to control tumour growth, the effects of such therapies are much wider, as affecting the vessel structure deeply modifies the microenvironment of the tumour mass. The aim of this review is to provide an overview of current knowledge on the global effects of anti-angiogenic treatment, mostly TKIs, on the shaping of the immune component of the RCC microenvironment. The data supporting the modification of immunity by anti-angiogenic therapies are collected to reveal the potential of angiogenesis modulation as a strategy for the adjuvant anti-cancer approach in immunotherapy. Termedia Publishing House 2018-03-05 2018-03 /pmc/articles/PMC5885083/ /pubmed/29628789 http://dx.doi.org/10.5114/wo.2018.73878 Text en Copyright: © 2018 Termedia Sp. z o. o. http://creativecommons.org/licenses/by-nc-sa/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) License, allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, provided the original work is properly cited and states its license.
spellingShingle Review
Brodaczewska, Klaudia K.
Szczylik, Cezary
Kieda, Claudine
Immune consequences of anti-angiogenic therapyin renal cell carcinoma
title Immune consequences of anti-angiogenic therapyin renal cell carcinoma
title_full Immune consequences of anti-angiogenic therapyin renal cell carcinoma
title_fullStr Immune consequences of anti-angiogenic therapyin renal cell carcinoma
title_full_unstemmed Immune consequences of anti-angiogenic therapyin renal cell carcinoma
title_short Immune consequences of anti-angiogenic therapyin renal cell carcinoma
title_sort immune consequences of anti-angiogenic therapyin renal cell carcinoma
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5885083/
https://www.ncbi.nlm.nih.gov/pubmed/29628789
http://dx.doi.org/10.5114/wo.2018.73878
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