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A phase I pilot study evaluating the beneficial effects of black raspberries in patients with Barrett’s esophagus
Black raspberries inhibit a broad range of cancers in preclinical models which has led to clinical evaluations targeting premalignant lesions of the colon, oral cavity and esophagus. A phase I pilot study was conducted in twenty Barrett's esophagus (BE) patients to investigate the effect of lyo...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6219678/ https://www.ncbi.nlm.nih.gov/pubmed/30450163 http://dx.doi.org/10.18632/oncotarget.10457 |
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author | Kresty, Laura A. Fromkes, John J. Frankel, Wendy L. Hammond, Cynthia D. Seeram, Navindra P. Baird, Maureen Stoner, Gary D. |
author_facet | Kresty, Laura A. Fromkes, John J. Frankel, Wendy L. Hammond, Cynthia D. Seeram, Navindra P. Baird, Maureen Stoner, Gary D. |
author_sort | Kresty, Laura A. |
collection | PubMed |
description | Black raspberries inhibit a broad range of cancers in preclinical models which has led to clinical evaluations targeting premalignant lesions of the colon, oral cavity and esophagus. A phase I pilot study was conducted in twenty Barrett's esophagus (BE) patients to investigate the effect of lyophilized black raspberries (LBR) on urinary metabolites and markers of lipid peroxidation, DNA damage and tissue markers of cellular proliferation, detoxification, and inflammation. Surveys, biopsies, blood and urine samples were collected before and after 6 months of LBR treatment (32 or 45 g). LBR significantly reduced urinary excretion of 8-epi-prostaglandin F2α, a marker of lipid peroxidation linked to oxidative stress and free radical damage. Urinary levels of the ellagitannin metabolites, urolithin A-glucuronide, urolithin A-sulfate and dimethylellagic acid glucuronide were significantly increased following 12 and 26 weeks of LBR consumption and may prove useful as indicators of compliance in future clinical studies. Immunohistochemical staining of BE biopsies following LBR treatment showed significant increases in mean GST-pi levels, with 55.6% of subjects responding favorably. In summary, LBR significantly decreased urinary lipid peroxidation levels and significantly increased GST-pi, a marker of detoxification, in BE epithelium. Still, LBR may need to be formulated differently, administered at higher concentrations or multiple times a day to increase efficacy. |
format | Online Article Text |
id | pubmed-6219678 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-62196782018-11-16 A phase I pilot study evaluating the beneficial effects of black raspberries in patients with Barrett’s esophagus Kresty, Laura A. Fromkes, John J. Frankel, Wendy L. Hammond, Cynthia D. Seeram, Navindra P. Baird, Maureen Stoner, Gary D. Oncotarget Clinical Research Paper Black raspberries inhibit a broad range of cancers in preclinical models which has led to clinical evaluations targeting premalignant lesions of the colon, oral cavity and esophagus. A phase I pilot study was conducted in twenty Barrett's esophagus (BE) patients to investigate the effect of lyophilized black raspberries (LBR) on urinary metabolites and markers of lipid peroxidation, DNA damage and tissue markers of cellular proliferation, detoxification, and inflammation. Surveys, biopsies, blood and urine samples were collected before and after 6 months of LBR treatment (32 or 45 g). LBR significantly reduced urinary excretion of 8-epi-prostaglandin F2α, a marker of lipid peroxidation linked to oxidative stress and free radical damage. Urinary levels of the ellagitannin metabolites, urolithin A-glucuronide, urolithin A-sulfate and dimethylellagic acid glucuronide were significantly increased following 12 and 26 weeks of LBR consumption and may prove useful as indicators of compliance in future clinical studies. Immunohistochemical staining of BE biopsies following LBR treatment showed significant increases in mean GST-pi levels, with 55.6% of subjects responding favorably. In summary, LBR significantly decreased urinary lipid peroxidation levels and significantly increased GST-pi, a marker of detoxification, in BE epithelium. Still, LBR may need to be formulated differently, administered at higher concentrations or multiple times a day to increase efficacy. Impact Journals LLC 2016-07-07 /pmc/articles/PMC6219678/ /pubmed/30450163 http://dx.doi.org/10.18632/oncotarget.10457 Text en Copyright: © 2018 Kresty et al. http://creativecommons.org/licenses/by/3.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) (CC-BY), which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Clinical Research Paper Kresty, Laura A. Fromkes, John J. Frankel, Wendy L. Hammond, Cynthia D. Seeram, Navindra P. Baird, Maureen Stoner, Gary D. A phase I pilot study evaluating the beneficial effects of black raspberries in patients with Barrett’s esophagus |
title | A phase I pilot study evaluating the beneficial effects of black raspberries in patients with Barrett’s esophagus |
title_full | A phase I pilot study evaluating the beneficial effects of black raspberries in patients with Barrett’s esophagus |
title_fullStr | A phase I pilot study evaluating the beneficial effects of black raspberries in patients with Barrett’s esophagus |
title_full_unstemmed | A phase I pilot study evaluating the beneficial effects of black raspberries in patients with Barrett’s esophagus |
title_short | A phase I pilot study evaluating the beneficial effects of black raspberries in patients with Barrett’s esophagus |
title_sort | phase i pilot study evaluating the beneficial effects of black raspberries in patients with barrett’s esophagus |
topic | Clinical Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6219678/ https://www.ncbi.nlm.nih.gov/pubmed/30450163 http://dx.doi.org/10.18632/oncotarget.10457 |
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