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Mitochondrial Peroxiredoxin III is a Potential Target for Cancer Therapy
Mitochondria are involved either directly or indirectly in oncogenesis and the alteration of metabolism in cancer cells. Cancer cells contain large numbers of abnormal mitochondria and produce large amounts of reactive oxygen species (ROS). Oxidative stress is caused by an imbalance between the prod...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Molecular Diversity Preservation International (MDPI)
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3211031/ https://www.ncbi.nlm.nih.gov/pubmed/22072940 http://dx.doi.org/10.3390/ijms12107163 |
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author | Song, In-Sung Kim, Hyoung-Kyu Jeong, Seung-Hun Lee, Sung-Ryul Kim, Nari Rhee, Byoung Doo Ko, Kyung Soo Han, Jin |
author_facet | Song, In-Sung Kim, Hyoung-Kyu Jeong, Seung-Hun Lee, Sung-Ryul Kim, Nari Rhee, Byoung Doo Ko, Kyung Soo Han, Jin |
author_sort | Song, In-Sung |
collection | PubMed |
description | Mitochondria are involved either directly or indirectly in oncogenesis and the alteration of metabolism in cancer cells. Cancer cells contain large numbers of abnormal mitochondria and produce large amounts of reactive oxygen species (ROS). Oxidative stress is caused by an imbalance between the production of ROS and the antioxidant capacity of the cell. Several cancer therapies, such as chemotherapeutic drugs and radiation, disrupt mitochondrial homeostasis and release cytochrome c, leading to apoptosome formation, which activates the intrinsic pathway. This is modulated by the extent of mitochondrial oxidative stress. The peroxiredoxin (Prx) system is a cellular defense system against oxidative stress, and mitochondria in cancer cells are known to contain high levels of Prx III. Here, we review accumulating evidence suggesting that mitochondrial oxidative stress is involved in cancer, and discuss the role of the mitochondrial Prx III antioxidant system as a potential target for cancer therapy. We hope that this review will provide the basis for new strategic approaches in the development of effective cancer treatments. |
format | Online Article Text |
id | pubmed-3211031 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Molecular Diversity Preservation International (MDPI) |
record_format | MEDLINE/PubMed |
spelling | pubmed-32110312011-11-09 Mitochondrial Peroxiredoxin III is a Potential Target for Cancer Therapy Song, In-Sung Kim, Hyoung-Kyu Jeong, Seung-Hun Lee, Sung-Ryul Kim, Nari Rhee, Byoung Doo Ko, Kyung Soo Han, Jin Int J Mol Sci Review Mitochondria are involved either directly or indirectly in oncogenesis and the alteration of metabolism in cancer cells. Cancer cells contain large numbers of abnormal mitochondria and produce large amounts of reactive oxygen species (ROS). Oxidative stress is caused by an imbalance between the production of ROS and the antioxidant capacity of the cell. Several cancer therapies, such as chemotherapeutic drugs and radiation, disrupt mitochondrial homeostasis and release cytochrome c, leading to apoptosome formation, which activates the intrinsic pathway. This is modulated by the extent of mitochondrial oxidative stress. The peroxiredoxin (Prx) system is a cellular defense system against oxidative stress, and mitochondria in cancer cells are known to contain high levels of Prx III. Here, we review accumulating evidence suggesting that mitochondrial oxidative stress is involved in cancer, and discuss the role of the mitochondrial Prx III antioxidant system as a potential target for cancer therapy. We hope that this review will provide the basis for new strategic approaches in the development of effective cancer treatments. Molecular Diversity Preservation International (MDPI) 2011-10-21 /pmc/articles/PMC3211031/ /pubmed/22072940 http://dx.doi.org/10.3390/ijms12107163 Text en © 2011 by the authors; licensee MDPI, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0 This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Review Song, In-Sung Kim, Hyoung-Kyu Jeong, Seung-Hun Lee, Sung-Ryul Kim, Nari Rhee, Byoung Doo Ko, Kyung Soo Han, Jin Mitochondrial Peroxiredoxin III is a Potential Target for Cancer Therapy |
title | Mitochondrial Peroxiredoxin III is a Potential Target for Cancer Therapy |
title_full | Mitochondrial Peroxiredoxin III is a Potential Target for Cancer Therapy |
title_fullStr | Mitochondrial Peroxiredoxin III is a Potential Target for Cancer Therapy |
title_full_unstemmed | Mitochondrial Peroxiredoxin III is a Potential Target for Cancer Therapy |
title_short | Mitochondrial Peroxiredoxin III is a Potential Target for Cancer Therapy |
title_sort | mitochondrial peroxiredoxin iii is a potential target for cancer therapy |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3211031/ https://www.ncbi.nlm.nih.gov/pubmed/22072940 http://dx.doi.org/10.3390/ijms12107163 |
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