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Chemopreventive Potential of 2,3,5,4′-Tetrahydroxystilbene-2-O-β-D-glucoside on the Formation of Aberrant Crypt Foci in Azoxymethane-Induced Colorectal Cancer in Rats

2,3,5,4′-Tetrahydroxystilbene-2-O-β-D-glucoside (THSG) has been shown to have antioxidative and anti-inflammatory effects. Oxidative and inflammatory reactions are related to the development of colorectal carcinoma (CRC). In the present study, we characterized the preventive activities of THSG on co...

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Autores principales: Lin, Chien-Liang, Jeng, Jiiang-Huei, Wu, Chih-Chung, Hsieh, Shu-Ling, Huang, Guan-Cheng, Leung, Wan, Lee, Chining-Ting, Chen, Chung-Yi, Lee, Chien-Hsing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5697369/
https://www.ncbi.nlm.nih.gov/pubmed/29238715
http://dx.doi.org/10.1155/2017/3634915
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author Lin, Chien-Liang
Jeng, Jiiang-Huei
Wu, Chih-Chung
Hsieh, Shu-Ling
Huang, Guan-Cheng
Leung, Wan
Lee, Chining-Ting
Chen, Chung-Yi
Lee, Chien-Hsing
author_facet Lin, Chien-Liang
Jeng, Jiiang-Huei
Wu, Chih-Chung
Hsieh, Shu-Ling
Huang, Guan-Cheng
Leung, Wan
Lee, Chining-Ting
Chen, Chung-Yi
Lee, Chien-Hsing
author_sort Lin, Chien-Liang
collection PubMed
description 2,3,5,4′-Tetrahydroxystilbene-2-O-β-D-glucoside (THSG) has been shown to have antioxidative and anti-inflammatory effects. Oxidative and inflammatory reactions are related to the development of colorectal carcinoma (CRC). In the present study, we characterized the preventive activities of THSG on colon carcinogenesis using the azoxymethane- (AOM-) mediated rat colon carcinogenesis model. F344 male rats were randomly divided into 5 groups (untreated and AOM model rats treated with or without THSG at 30, 150, or 250 mg/kg) after which the numbers of aberrant crypt foci (ACF) were assessed in the colon tissues of all rats. The expressions of nuclear factor-κB (NF-κB), cyclooxygenase-2 (COX-2), matrix metalloproteinase proteins (MMPs), and carcinoembryonic antigen (CEA) were measured as effective early predictors of CRC using western blot analysis. Treatment with THSG (150 or 250 mg/kg) induced a 50% reduction in total colonic ACF formation (P < 0.05). Furthermore, our results revealed a downregulation of CEA and NF-κB protein levels in the reduced number of ACF elicited by treatment with THSG, whereas levels of COX-2 and MMPs proteins were not changed. Collectively, THSG may be a promising natural lead compound or drug candidate for treating early phases of CRC.
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spelling pubmed-56973692017-12-13 Chemopreventive Potential of 2,3,5,4′-Tetrahydroxystilbene-2-O-β-D-glucoside on the Formation of Aberrant Crypt Foci in Azoxymethane-Induced Colorectal Cancer in Rats Lin, Chien-Liang Jeng, Jiiang-Huei Wu, Chih-Chung Hsieh, Shu-Ling Huang, Guan-Cheng Leung, Wan Lee, Chining-Ting Chen, Chung-Yi Lee, Chien-Hsing Biomed Res Int Research Article 2,3,5,4′-Tetrahydroxystilbene-2-O-β-D-glucoside (THSG) has been shown to have antioxidative and anti-inflammatory effects. Oxidative and inflammatory reactions are related to the development of colorectal carcinoma (CRC). In the present study, we characterized the preventive activities of THSG on colon carcinogenesis using the azoxymethane- (AOM-) mediated rat colon carcinogenesis model. F344 male rats were randomly divided into 5 groups (untreated and AOM model rats treated with or without THSG at 30, 150, or 250 mg/kg) after which the numbers of aberrant crypt foci (ACF) were assessed in the colon tissues of all rats. The expressions of nuclear factor-κB (NF-κB), cyclooxygenase-2 (COX-2), matrix metalloproteinase proteins (MMPs), and carcinoembryonic antigen (CEA) were measured as effective early predictors of CRC using western blot analysis. Treatment with THSG (150 or 250 mg/kg) induced a 50% reduction in total colonic ACF formation (P < 0.05). Furthermore, our results revealed a downregulation of CEA and NF-κB protein levels in the reduced number of ACF elicited by treatment with THSG, whereas levels of COX-2 and MMPs proteins were not changed. Collectively, THSG may be a promising natural lead compound or drug candidate for treating early phases of CRC. Hindawi 2017 2017-11-07 /pmc/articles/PMC5697369/ /pubmed/29238715 http://dx.doi.org/10.1155/2017/3634915 Text en Copyright © 2017 Chien-Liang Lin et al. https://creativecommons.org/licenses/by/4.0/ 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 Research Article
Lin, Chien-Liang
Jeng, Jiiang-Huei
Wu, Chih-Chung
Hsieh, Shu-Ling
Huang, Guan-Cheng
Leung, Wan
Lee, Chining-Ting
Chen, Chung-Yi
Lee, Chien-Hsing
Chemopreventive Potential of 2,3,5,4′-Tetrahydroxystilbene-2-O-β-D-glucoside on the Formation of Aberrant Crypt Foci in Azoxymethane-Induced Colorectal Cancer in Rats
title Chemopreventive Potential of 2,3,5,4′-Tetrahydroxystilbene-2-O-β-D-glucoside on the Formation of Aberrant Crypt Foci in Azoxymethane-Induced Colorectal Cancer in Rats
title_full Chemopreventive Potential of 2,3,5,4′-Tetrahydroxystilbene-2-O-β-D-glucoside on the Formation of Aberrant Crypt Foci in Azoxymethane-Induced Colorectal Cancer in Rats
title_fullStr Chemopreventive Potential of 2,3,5,4′-Tetrahydroxystilbene-2-O-β-D-glucoside on the Formation of Aberrant Crypt Foci in Azoxymethane-Induced Colorectal Cancer in Rats
title_full_unstemmed Chemopreventive Potential of 2,3,5,4′-Tetrahydroxystilbene-2-O-β-D-glucoside on the Formation of Aberrant Crypt Foci in Azoxymethane-Induced Colorectal Cancer in Rats
title_short Chemopreventive Potential of 2,3,5,4′-Tetrahydroxystilbene-2-O-β-D-glucoside on the Formation of Aberrant Crypt Foci in Azoxymethane-Induced Colorectal Cancer in Rats
title_sort chemopreventive potential of 2,3,5,4′-tetrahydroxystilbene-2-o-β-d-glucoside on the formation of aberrant crypt foci in azoxymethane-induced colorectal cancer in rats
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5697369/
https://www.ncbi.nlm.nih.gov/pubmed/29238715
http://dx.doi.org/10.1155/2017/3634915
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