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Increased Plasma Superoxide Radical in Patients with Non-Metastatic Colorectal Cancer

BACKGROUND: Several studies have investigated the potential role of oxidative stress in the evolution of colorectal cancer. In most of these studies, oxidative stress was assessed indirectly by measurements of indices like lipid peroxidation, protein oxidation or antioxidant status. The present stud...

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Autores principales: Assimakopoulos, Stelios F., Grintzalis, Konstantinos, Papapostolou, Ioannis, Thomopoulos, Konstantinos C., Georgiou, Christos D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elmer Press 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5154215/
https://www.ncbi.nlm.nih.gov/pubmed/27994706
http://dx.doi.org/10.4021/gr2008.11.1249
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author Assimakopoulos, Stelios F.
Grintzalis, Konstantinos
Papapostolou, Ioannis
Thomopoulos, Konstantinos C.
Georgiou, Christos D.
author_facet Assimakopoulos, Stelios F.
Grintzalis, Konstantinos
Papapostolou, Ioannis
Thomopoulos, Konstantinos C.
Georgiou, Christos D.
author_sort Assimakopoulos, Stelios F.
collection PubMed
description BACKGROUND: Several studies have investigated the potential role of oxidative stress in the evolution of colorectal cancer. In most of these studies, oxidative stress was assessed indirectly by measurements of indices like lipid peroxidation, protein oxidation or antioxidant status. The present study was undertaken to directly assess systemic oxidative stress by measuring plasma superoxide radical (O(2)(-)·) in patients with non-metastatic colorectal cancer. METHODS: Twelve patients (6 males and 6 females) with a recent diagnosis of colorectal cancer and no signs of metastases and 12 healthy volunteers matched for age and gender were enrolled in the study. O(2)(-)· levels in plasma were assessed by application of a new ultra-sensitive fluorescent assay. Also lipid peroxidation levels in plasma were measured as thiobarbituric acid reactive species (TBARS). RESULTS: In the plasma fraction of whole blood, there was a significant increase (47%) of O(2)(-)· levels in colorectal carcinoma patients as compared to healthy volunteers (P < 0.001). In fractionated plasma, no O(2)(-)· was detected in both groups. Plasma TBARS levels were increased by 81% in colorectal carcinoma patients as compared to controls (P < 0.001). CONCLUSIONS: These data show that colorectal cancer, even at early (non-metastatic) stages, induces systemic oxidative stress as evidenced by increased O(2)·(-) levels measured in plasma. Given the important role of oxidative stress in carcinogenesis and the fact that O(2)·(-) is considered its primary parameter, our findings if confirmed in larger studies might establish the potential validity of O(2)·(-) as a new biomarker for colorectal cancer.
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spelling pubmed-51542152016-12-19 Increased Plasma Superoxide Radical in Patients with Non-Metastatic Colorectal Cancer Assimakopoulos, Stelios F. Grintzalis, Konstantinos Papapostolou, Ioannis Thomopoulos, Konstantinos C. Georgiou, Christos D. Gastroenterology Res Original Article BACKGROUND: Several studies have investigated the potential role of oxidative stress in the evolution of colorectal cancer. In most of these studies, oxidative stress was assessed indirectly by measurements of indices like lipid peroxidation, protein oxidation or antioxidant status. The present study was undertaken to directly assess systemic oxidative stress by measuring plasma superoxide radical (O(2)(-)·) in patients with non-metastatic colorectal cancer. METHODS: Twelve patients (6 males and 6 females) with a recent diagnosis of colorectal cancer and no signs of metastases and 12 healthy volunteers matched for age and gender were enrolled in the study. O(2)(-)· levels in plasma were assessed by application of a new ultra-sensitive fluorescent assay. Also lipid peroxidation levels in plasma were measured as thiobarbituric acid reactive species (TBARS). RESULTS: In the plasma fraction of whole blood, there was a significant increase (47%) of O(2)(-)· levels in colorectal carcinoma patients as compared to healthy volunteers (P < 0.001). In fractionated plasma, no O(2)(-)· was detected in both groups. Plasma TBARS levels were increased by 81% in colorectal carcinoma patients as compared to controls (P < 0.001). CONCLUSIONS: These data show that colorectal cancer, even at early (non-metastatic) stages, induces systemic oxidative stress as evidenced by increased O(2)·(-) levels measured in plasma. Given the important role of oxidative stress in carcinogenesis and the fact that O(2)·(-) is considered its primary parameter, our findings if confirmed in larger studies might establish the potential validity of O(2)·(-) as a new biomarker for colorectal cancer. Elmer Press 2008-12 2008-11-20 /pmc/articles/PMC5154215/ /pubmed/27994706 http://dx.doi.org/10.4021/gr2008.11.1249 Text en Copyright 2008, Assimakopoulos et al. http://creativecommons.org/licenses/by/2.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Assimakopoulos, Stelios F.
Grintzalis, Konstantinos
Papapostolou, Ioannis
Thomopoulos, Konstantinos C.
Georgiou, Christos D.
Increased Plasma Superoxide Radical in Patients with Non-Metastatic Colorectal Cancer
title Increased Plasma Superoxide Radical in Patients with Non-Metastatic Colorectal Cancer
title_full Increased Plasma Superoxide Radical in Patients with Non-Metastatic Colorectal Cancer
title_fullStr Increased Plasma Superoxide Radical in Patients with Non-Metastatic Colorectal Cancer
title_full_unstemmed Increased Plasma Superoxide Radical in Patients with Non-Metastatic Colorectal Cancer
title_short Increased Plasma Superoxide Radical in Patients with Non-Metastatic Colorectal Cancer
title_sort increased plasma superoxide radical in patients with non-metastatic colorectal cancer
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5154215/
https://www.ncbi.nlm.nih.gov/pubmed/27994706
http://dx.doi.org/10.4021/gr2008.11.1249
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