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The mechanistic immunosuppressive role of the tumour vasculature and potential nanoparticle-mediated therapeutic strategies
The tumour vasculature is well-established to display irregular structure and hierarchy that is conducive to promoting tumour growth and metastasis while maintaining immunosuppression. As tumours grow, their metabolic rate increases while their distance from blood vessels furthers, generating a hypo...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9423123/ https://www.ncbi.nlm.nih.gov/pubmed/36045675 http://dx.doi.org/10.3389/fimmu.2022.976677 |
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author | Ileiwat, Zakaria Elias Tabish, Tanveer A. Zinovkin, Dmitry A. Yuzugulen, Jale Arghiani, Nahid Pranjol, Md Zahidul I. |
author_facet | Ileiwat, Zakaria Elias Tabish, Tanveer A. Zinovkin, Dmitry A. Yuzugulen, Jale Arghiani, Nahid Pranjol, Md Zahidul I. |
author_sort | Ileiwat, Zakaria Elias |
collection | PubMed |
description | The tumour vasculature is well-established to display irregular structure and hierarchy that is conducive to promoting tumour growth and metastasis while maintaining immunosuppression. As tumours grow, their metabolic rate increases while their distance from blood vessels furthers, generating a hypoxic and acidic tumour microenvironment. Consequently, cancer cells upregulate the expression of pro-angiogenic factors which propagate aberrant blood vessel formation. This generates atypical vascular features that reduce chemotherapy, radiotherapy, and immunotherapy efficacy. Therefore, the development of therapies aiming to restore the vasculature to a functional state remains a necessary research target. Many anti-angiogenic therapies aim to target this such as bevacizumab or sunitinib but have shown variable efficacy in solid tumours due to intrinsic or acquired resistance. Therefore, novel therapeutic strategies such as combination therapies and nanotechnology-mediated therapies may provide alternatives to overcoming the barriers generated by the tumour vasculature. This review summarises the mechanisms that induce abnormal tumour angiogenesis and how the vasculature’s features elicit immunosuppression. Furthermore, the review explores examples of treatment regiments that target the tumour vasculature. |
format | Online Article Text |
id | pubmed-9423123 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-94231232022-08-30 The mechanistic immunosuppressive role of the tumour vasculature and potential nanoparticle-mediated therapeutic strategies Ileiwat, Zakaria Elias Tabish, Tanveer A. Zinovkin, Dmitry A. Yuzugulen, Jale Arghiani, Nahid Pranjol, Md Zahidul I. Front Immunol Immunology The tumour vasculature is well-established to display irregular structure and hierarchy that is conducive to promoting tumour growth and metastasis while maintaining immunosuppression. As tumours grow, their metabolic rate increases while their distance from blood vessels furthers, generating a hypoxic and acidic tumour microenvironment. Consequently, cancer cells upregulate the expression of pro-angiogenic factors which propagate aberrant blood vessel formation. This generates atypical vascular features that reduce chemotherapy, radiotherapy, and immunotherapy efficacy. Therefore, the development of therapies aiming to restore the vasculature to a functional state remains a necessary research target. Many anti-angiogenic therapies aim to target this such as bevacizumab or sunitinib but have shown variable efficacy in solid tumours due to intrinsic or acquired resistance. Therefore, novel therapeutic strategies such as combination therapies and nanotechnology-mediated therapies may provide alternatives to overcoming the barriers generated by the tumour vasculature. This review summarises the mechanisms that induce abnormal tumour angiogenesis and how the vasculature’s features elicit immunosuppression. Furthermore, the review explores examples of treatment regiments that target the tumour vasculature. Frontiers Media S.A. 2022-08-15 /pmc/articles/PMC9423123/ /pubmed/36045675 http://dx.doi.org/10.3389/fimmu.2022.976677 Text en Copyright © 2022 Ileiwat, Tabish, Zinovkin, Yuzugulen, Arghiani and Pranjol https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Immunology Ileiwat, Zakaria Elias Tabish, Tanveer A. Zinovkin, Dmitry A. Yuzugulen, Jale Arghiani, Nahid Pranjol, Md Zahidul I. The mechanistic immunosuppressive role of the tumour vasculature and potential nanoparticle-mediated therapeutic strategies |
title | The mechanistic immunosuppressive role of the tumour vasculature and potential nanoparticle-mediated therapeutic strategies |
title_full | The mechanistic immunosuppressive role of the tumour vasculature and potential nanoparticle-mediated therapeutic strategies |
title_fullStr | The mechanistic immunosuppressive role of the tumour vasculature and potential nanoparticle-mediated therapeutic strategies |
title_full_unstemmed | The mechanistic immunosuppressive role of the tumour vasculature and potential nanoparticle-mediated therapeutic strategies |
title_short | The mechanistic immunosuppressive role of the tumour vasculature and potential nanoparticle-mediated therapeutic strategies |
title_sort | mechanistic immunosuppressive role of the tumour vasculature and potential nanoparticle-mediated therapeutic strategies |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9423123/ https://www.ncbi.nlm.nih.gov/pubmed/36045675 http://dx.doi.org/10.3389/fimmu.2022.976677 |
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