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Targeting Nitric Oxide: Say NO to Metastasis
Utilizing targeted therapies capable of reducing cancer metastasis, targeting chemoresistant and self-renewing cancer stem cells, and augmenting the efficacy of systemic chemo/radiotherapies is vital to minimize cancer-associated mortality. Targeting nitric oxide synthase (NOS), a protein within the...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for Cancer Research
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10183809/ https://www.ncbi.nlm.nih.gov/pubmed/36520504 http://dx.doi.org/10.1158/1078-0432.CCR-22-2791 |
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author | Reddy, Tejaswini P. Glynn, Sharon A. Billiar, Timothy R. Wink, David A. Chang, Jenny C. |
author_facet | Reddy, Tejaswini P. Glynn, Sharon A. Billiar, Timothy R. Wink, David A. Chang, Jenny C. |
author_sort | Reddy, Tejaswini P. |
collection | PubMed |
description | Utilizing targeted therapies capable of reducing cancer metastasis, targeting chemoresistant and self-renewing cancer stem cells, and augmenting the efficacy of systemic chemo/radiotherapies is vital to minimize cancer-associated mortality. Targeting nitric oxide synthase (NOS), a protein within the tumor microenvironment, has gained interest as a promising therapeutic strategy to reduce metastatic capacity and augment the efficacy of chemo/radiotherapies in various solid malignancies. Our review highlights the influence of nitric oxide (NO) in tumor progression and cancer metastasis, as well as promising preclinical studies that evaluated NOS inhibitors as anticancer therapies. Lastly, we highlight the prospects and outstanding challenges of using NOS inhibitors in the clinical setting. |
format | Online Article Text |
id | pubmed-10183809 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Association for Cancer Research |
record_format | MEDLINE/PubMed |
spelling | pubmed-101838092023-05-16 Targeting Nitric Oxide: Say NO to Metastasis Reddy, Tejaswini P. Glynn, Sharon A. Billiar, Timothy R. Wink, David A. Chang, Jenny C. Clin Cancer Res Reviews Utilizing targeted therapies capable of reducing cancer metastasis, targeting chemoresistant and self-renewing cancer stem cells, and augmenting the efficacy of systemic chemo/radiotherapies is vital to minimize cancer-associated mortality. Targeting nitric oxide synthase (NOS), a protein within the tumor microenvironment, has gained interest as a promising therapeutic strategy to reduce metastatic capacity and augment the efficacy of chemo/radiotherapies in various solid malignancies. Our review highlights the influence of nitric oxide (NO) in tumor progression and cancer metastasis, as well as promising preclinical studies that evaluated NOS inhibitors as anticancer therapies. Lastly, we highlight the prospects and outstanding challenges of using NOS inhibitors in the clinical setting. American Association for Cancer Research 2023-05-15 2022-12-15 /pmc/articles/PMC10183809/ /pubmed/36520504 http://dx.doi.org/10.1158/1078-0432.CCR-22-2791 Text en ©2022 The Authors; Published by the American Association for Cancer Research https://creativecommons.org/licenses/by-nc-nd/4.0/This open access article is distributed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0) license. |
spellingShingle | Reviews Reddy, Tejaswini P. Glynn, Sharon A. Billiar, Timothy R. Wink, David A. Chang, Jenny C. Targeting Nitric Oxide: Say NO to Metastasis |
title | Targeting Nitric Oxide: Say NO to Metastasis |
title_full | Targeting Nitric Oxide: Say NO to Metastasis |
title_fullStr | Targeting Nitric Oxide: Say NO to Metastasis |
title_full_unstemmed | Targeting Nitric Oxide: Say NO to Metastasis |
title_short | Targeting Nitric Oxide: Say NO to Metastasis |
title_sort | targeting nitric oxide: say no to metastasis |
topic | Reviews |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10183809/ https://www.ncbi.nlm.nih.gov/pubmed/36520504 http://dx.doi.org/10.1158/1078-0432.CCR-22-2791 |
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