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Modulation of heme and tumor vascular oxygenation- a novel strategy for lung cancer therapy

Hypoxia and faulty vasculature are well-known hallmarks of cancer and in addition to being associated with poor prognosis in patients, these hallmarks are also known to contribute to therapy resistance. In recent years, therapeutics that alleviate hypoxia and promote normalization of vasculature are...

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Detalles Bibliográficos
Autores principales: Ghosh, Poorva, Mason, Ralph P., Liu, Li, Zhang, Li
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9718586/
https://www.ncbi.nlm.nih.gov/pubmed/36471789
http://dx.doi.org/10.18632/oncoscience.569
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author Ghosh, Poorva
Mason, Ralph P.
Liu, Li
Zhang, Li
author_facet Ghosh, Poorva
Mason, Ralph P.
Liu, Li
Zhang, Li
author_sort Ghosh, Poorva
collection PubMed
description Hypoxia and faulty vasculature are well-known hallmarks of cancer and in addition to being associated with poor prognosis in patients, these hallmarks are also known to contribute to therapy resistance. In recent years, therapeutics that alleviate hypoxia and promote normalization of vasculature are being explored for cancer therapy. In addition to being hypoxic, cancers such as non-small cell lung cancers exhibit elevated oxidative phosphorylation. Therapeutic strategies that can normalize vasculature and reduce oxidative phosphorylation could greatly benefit the landscape of cancer therapeutics. Here, we highlight a heme-targeting therapeutic strategy that demonstrates significant tumor growth inhibition in non-small cell lung cancer mouse models using multi-spectral optoacoustic tomography.
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spelling pubmed-97185862022-12-04 Modulation of heme and tumor vascular oxygenation- a novel strategy for lung cancer therapy Ghosh, Poorva Mason, Ralph P. Liu, Li Zhang, Li Oncoscience Research Perspective Hypoxia and faulty vasculature are well-known hallmarks of cancer and in addition to being associated with poor prognosis in patients, these hallmarks are also known to contribute to therapy resistance. In recent years, therapeutics that alleviate hypoxia and promote normalization of vasculature are being explored for cancer therapy. In addition to being hypoxic, cancers such as non-small cell lung cancers exhibit elevated oxidative phosphorylation. Therapeutic strategies that can normalize vasculature and reduce oxidative phosphorylation could greatly benefit the landscape of cancer therapeutics. Here, we highlight a heme-targeting therapeutic strategy that demonstrates significant tumor growth inhibition in non-small cell lung cancer mouse models using multi-spectral optoacoustic tomography. Impact Journals LLC 2022-12-02 /pmc/articles/PMC9718586/ /pubmed/36471789 http://dx.doi.org/10.18632/oncoscience.569 Text en https://creativecommons.org/licenses/by/3.0/Copyright: © 2022 Ghosh et al. This is an open access article distributed under the terms of the Creative Commons Attribution License (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Perspective
Ghosh, Poorva
Mason, Ralph P.
Liu, Li
Zhang, Li
Modulation of heme and tumor vascular oxygenation- a novel strategy for lung cancer therapy
title Modulation of heme and tumor vascular oxygenation- a novel strategy for lung cancer therapy
title_full Modulation of heme and tumor vascular oxygenation- a novel strategy for lung cancer therapy
title_fullStr Modulation of heme and tumor vascular oxygenation- a novel strategy for lung cancer therapy
title_full_unstemmed Modulation of heme and tumor vascular oxygenation- a novel strategy for lung cancer therapy
title_short Modulation of heme and tumor vascular oxygenation- a novel strategy for lung cancer therapy
title_sort modulation of heme and tumor vascular oxygenation- a novel strategy for lung cancer therapy
topic Research Perspective
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9718586/
https://www.ncbi.nlm.nih.gov/pubmed/36471789
http://dx.doi.org/10.18632/oncoscience.569
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