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Next-Generation Anti-Angiogenic Therapies as a Future Prospect for Glioma Immunotherapy; From Bench to Bedside
Glioblastoma (grade IV glioma) is the most aggressive histopathological subtype of glial tumors with inordinate microvascular proliferation as one of its key pathological features. Extensive angiogenesis in the tumor microenvironment supplies oxygen and nutrients to tumoral cells; retains their surv...
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/PMC9231436/ https://www.ncbi.nlm.nih.gov/pubmed/35757736 http://dx.doi.org/10.3389/fimmu.2022.859633 |
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author | Shamshiripour, Parisa Hajiahmadi, Fahimeh Lotfi, Shahla Esmaeili, Niloofar Robab Zare, Amir Akbarpour, Mahzad Ahmadvand, Davoud |
author_facet | Shamshiripour, Parisa Hajiahmadi, Fahimeh Lotfi, Shahla Esmaeili, Niloofar Robab Zare, Amir Akbarpour, Mahzad Ahmadvand, Davoud |
author_sort | Shamshiripour, Parisa |
collection | PubMed |
description | Glioblastoma (grade IV glioma) is the most aggressive histopathological subtype of glial tumors with inordinate microvascular proliferation as one of its key pathological features. Extensive angiogenesis in the tumor microenvironment supplies oxygen and nutrients to tumoral cells; retains their survival under hypoxic conditions; and induces an immunosuppressive microenvironment. Anti-angiogenesis therapy for high-grade gliomas has long been studied as an adjuvant immunotherapy strategy to overcome tumor growth. In the current review, we discussed the underlying molecular mechanisms contributing to glioblastoma aberrant angiogenesis. Further, we discussed clinical applications of monoclonal antibodies, tyrosine kinase inhibitors, and aptamers as three major subgroups of anti-angiogenic immunotherapeutics and their limitations. Moreover, we reviewed clinical and preclinical applications of small interfering RNAs (siRNAs) as the next-generation anti-angiogenic therapeutics and summarized their potential advantages and limitations. siRNAs may serve as next-generation anti-angiogenic therapeutics for glioma. Additionally, application of nanoparticles as a delivery vehicle could increase their selectivity and lower their off-target effects. |
format | Online Article Text |
id | pubmed-9231436 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-92314362022-06-25 Next-Generation Anti-Angiogenic Therapies as a Future Prospect for Glioma Immunotherapy; From Bench to Bedside Shamshiripour, Parisa Hajiahmadi, Fahimeh Lotfi, Shahla Esmaeili, Niloofar Robab Zare, Amir Akbarpour, Mahzad Ahmadvand, Davoud Front Immunol Immunology Glioblastoma (grade IV glioma) is the most aggressive histopathological subtype of glial tumors with inordinate microvascular proliferation as one of its key pathological features. Extensive angiogenesis in the tumor microenvironment supplies oxygen and nutrients to tumoral cells; retains their survival under hypoxic conditions; and induces an immunosuppressive microenvironment. Anti-angiogenesis therapy for high-grade gliomas has long been studied as an adjuvant immunotherapy strategy to overcome tumor growth. In the current review, we discussed the underlying molecular mechanisms contributing to glioblastoma aberrant angiogenesis. Further, we discussed clinical applications of monoclonal antibodies, tyrosine kinase inhibitors, and aptamers as three major subgroups of anti-angiogenic immunotherapeutics and their limitations. Moreover, we reviewed clinical and preclinical applications of small interfering RNAs (siRNAs) as the next-generation anti-angiogenic therapeutics and summarized their potential advantages and limitations. siRNAs may serve as next-generation anti-angiogenic therapeutics for glioma. Additionally, application of nanoparticles as a delivery vehicle could increase their selectivity and lower their off-target effects. Frontiers Media S.A. 2022-06-10 /pmc/articles/PMC9231436/ /pubmed/35757736 http://dx.doi.org/10.3389/fimmu.2022.859633 Text en Copyright © 2022 Shamshiripour, Hajiahmadi, Lotfi, Esmaeili, Zare, Akbarpour and Ahmadvand 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 Shamshiripour, Parisa Hajiahmadi, Fahimeh Lotfi, Shahla Esmaeili, Niloofar Robab Zare, Amir Akbarpour, Mahzad Ahmadvand, Davoud Next-Generation Anti-Angiogenic Therapies as a Future Prospect for Glioma Immunotherapy; From Bench to Bedside |
title | Next-Generation Anti-Angiogenic Therapies as a Future Prospect for Glioma Immunotherapy; From Bench to Bedside |
title_full | Next-Generation Anti-Angiogenic Therapies as a Future Prospect for Glioma Immunotherapy; From Bench to Bedside |
title_fullStr | Next-Generation Anti-Angiogenic Therapies as a Future Prospect for Glioma Immunotherapy; From Bench to Bedside |
title_full_unstemmed | Next-Generation Anti-Angiogenic Therapies as a Future Prospect for Glioma Immunotherapy; From Bench to Bedside |
title_short | Next-Generation Anti-Angiogenic Therapies as a Future Prospect for Glioma Immunotherapy; From Bench to Bedside |
title_sort | next-generation anti-angiogenic therapies as a future prospect for glioma immunotherapy; from bench to bedside |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9231436/ https://www.ncbi.nlm.nih.gov/pubmed/35757736 http://dx.doi.org/10.3389/fimmu.2022.859633 |
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