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Increased Oxidative Stress as a Selective Anticancer Therapy

Reactive oxygen species (ROS) are closely related to tumorgenesis. Under hypoxic environment, increased levels of ROS induce the expression of hypoxia inducible factors (HIFs) in cancer stem cells (CSCs), resulting in the promotion of the upregulation of CSC markers, and the reduction of intracellul...

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Detalles Bibliográficos
Autores principales: Liu, Jiahui, Wang, Zhichong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4529973/
https://www.ncbi.nlm.nih.gov/pubmed/26273420
http://dx.doi.org/10.1155/2015/294303
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author Liu, Jiahui
Wang, Zhichong
author_facet Liu, Jiahui
Wang, Zhichong
author_sort Liu, Jiahui
collection PubMed
description Reactive oxygen species (ROS) are closely related to tumorgenesis. Under hypoxic environment, increased levels of ROS induce the expression of hypoxia inducible factors (HIFs) in cancer stem cells (CSCs), resulting in the promotion of the upregulation of CSC markers, and the reduction of intracellular ROS level, thus facilitating CSCs survival and proliferation. Although the ROS level is regulated by powerful antioxidant defense mechanisms in cancer cells, it is observed to remain higher than that in normal cells. Cancer cells may be more sensitive than normal cells to the accumulation of ROS; consequently, it is supposed that increased oxidative stress by exogenous ROS generation therapy has an effect on selectively killing cancer cells without affecting normal cells. This paper reviews the mechanisms of redox regulation in CSCs and the pivotal role of ROS in anticancer treatment.
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spelling pubmed-45299732015-08-13 Increased Oxidative Stress as a Selective Anticancer Therapy Liu, Jiahui Wang, Zhichong Oxid Med Cell Longev Review Article Reactive oxygen species (ROS) are closely related to tumorgenesis. Under hypoxic environment, increased levels of ROS induce the expression of hypoxia inducible factors (HIFs) in cancer stem cells (CSCs), resulting in the promotion of the upregulation of CSC markers, and the reduction of intracellular ROS level, thus facilitating CSCs survival and proliferation. Although the ROS level is regulated by powerful antioxidant defense mechanisms in cancer cells, it is observed to remain higher than that in normal cells. Cancer cells may be more sensitive than normal cells to the accumulation of ROS; consequently, it is supposed that increased oxidative stress by exogenous ROS generation therapy has an effect on selectively killing cancer cells without affecting normal cells. This paper reviews the mechanisms of redox regulation in CSCs and the pivotal role of ROS in anticancer treatment. Hindawi Publishing Corporation 2015 2015-07-26 /pmc/articles/PMC4529973/ /pubmed/26273420 http://dx.doi.org/10.1155/2015/294303 Text en Copyright © 2015 J. Liu and Z. Wang. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Liu, Jiahui
Wang, Zhichong
Increased Oxidative Stress as a Selective Anticancer Therapy
title Increased Oxidative Stress as a Selective Anticancer Therapy
title_full Increased Oxidative Stress as a Selective Anticancer Therapy
title_fullStr Increased Oxidative Stress as a Selective Anticancer Therapy
title_full_unstemmed Increased Oxidative Stress as a Selective Anticancer Therapy
title_short Increased Oxidative Stress as a Selective Anticancer Therapy
title_sort increased oxidative stress as a selective anticancer therapy
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4529973/
https://www.ncbi.nlm.nih.gov/pubmed/26273420
http://dx.doi.org/10.1155/2015/294303
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