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Redox Regulation in Cancer Cells during Metastasis

Metastasis is an inefficient process in which the vast majority of cancer cells are fated to die, partly because they experience oxidative stress. Metastasizing cancer cells migrate through diverse environments that differ dramatically from their tumor of origin, leading to redox imbalances. The rar...

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Detalles Bibliográficos
Autores principales: Tasdogan, Alpaslan, Ubellacker, Jessalyn M., Morrison, Sean J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for Cancer Research 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8563381/
https://www.ncbi.nlm.nih.gov/pubmed/34649956
http://dx.doi.org/10.1158/2159-8290.CD-21-0558
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author Tasdogan, Alpaslan
Ubellacker, Jessalyn M.
Morrison, Sean J.
author_facet Tasdogan, Alpaslan
Ubellacker, Jessalyn M.
Morrison, Sean J.
author_sort Tasdogan, Alpaslan
collection PubMed
description Metastasis is an inefficient process in which the vast majority of cancer cells are fated to die, partly because they experience oxidative stress. Metastasizing cancer cells migrate through diverse environments that differ dramatically from their tumor of origin, leading to redox imbalances. The rare metastasizing cells that survive undergo reversible metabolic changes that confer oxidative stress resistance. We review the changes in redox regulation that cancer cells undergo during metastasis. By better understanding these mechanisms, it may be possible to develop pro-oxidant therapies that block disease progression by exacerbating oxidative stress in cancer cells. SIGNIFICANCE: Oxidative stress often limits cancer cell survival during metastasis, raising the possibility of inhibiting cancer progression with pro-oxidant therapies. This is the opposite strategy of treating patients with antioxidants, an approach that worsened outcomes in large clinical trials.
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spelling pubmed-85633812022-05-01 Redox Regulation in Cancer Cells during Metastasis Tasdogan, Alpaslan Ubellacker, Jessalyn M. Morrison, Sean J. Cancer Discov Mini Review Metastasis is an inefficient process in which the vast majority of cancer cells are fated to die, partly because they experience oxidative stress. Metastasizing cancer cells migrate through diverse environments that differ dramatically from their tumor of origin, leading to redox imbalances. The rare metastasizing cells that survive undergo reversible metabolic changes that confer oxidative stress resistance. We review the changes in redox regulation that cancer cells undergo during metastasis. By better understanding these mechanisms, it may be possible to develop pro-oxidant therapies that block disease progression by exacerbating oxidative stress in cancer cells. SIGNIFICANCE: Oxidative stress often limits cancer cell survival during metastasis, raising the possibility of inhibiting cancer progression with pro-oxidant therapies. This is the opposite strategy of treating patients with antioxidants, an approach that worsened outcomes in large clinical trials. American Association for Cancer Research 2021-11 2021-10-14 /pmc/articles/PMC8563381/ /pubmed/34649956 http://dx.doi.org/10.1158/2159-8290.CD-21-0558 Text en ©2021 The Authors; Published by the American Association for Cancer Research https://creativecommons.org/licenses/by/4.0/This open access article is distributed under the Creative Commons Attribution License 4.0 International (CC BY).
spellingShingle Mini Review
Tasdogan, Alpaslan
Ubellacker, Jessalyn M.
Morrison, Sean J.
Redox Regulation in Cancer Cells during Metastasis
title Redox Regulation in Cancer Cells during Metastasis
title_full Redox Regulation in Cancer Cells during Metastasis
title_fullStr Redox Regulation in Cancer Cells during Metastasis
title_full_unstemmed Redox Regulation in Cancer Cells during Metastasis
title_short Redox Regulation in Cancer Cells during Metastasis
title_sort redox regulation in cancer cells during metastasis
topic Mini Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8563381/
https://www.ncbi.nlm.nih.gov/pubmed/34649956
http://dx.doi.org/10.1158/2159-8290.CD-21-0558
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