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Epigallocatechin-3-gallate suppresses hemin-aggravated colon carcinogenesis through Nrf2-inhibited mitochondrial reactive oxygen species accumulation

BACKGROUND: Previous studies have presented evidence to support the significant association between red meat intake and colon cancer, suggesting that heme iron plays a key role in colon carcinogenesis. Epigallocatechin-3-gallate (EGCG), the major constituent of green tea, exhibits anti-oxidative and...

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Autores principales: Seok, Ju Hyung, Kim, Dae Hyun, Kim, Hye Jih, Jo, Hang Hyo, Kim, Eun Young, Jeong, Jae-Hwang, Park, Young Seok, Lee, Sang Hun, Kim, Dae Joong, Nam, Sang Yoon, Lee, Beom Jun, Lee, Hyun Jik
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society of Veterinary Science 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9523342/
https://www.ncbi.nlm.nih.gov/pubmed/36174978
http://dx.doi.org/10.4142/jvs.22097
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author Seok, Ju Hyung
Kim, Dae Hyun
Kim, Hye Jih
Jo, Hang Hyo
Kim, Eun Young
Jeong, Jae-Hwang
Park, Young Seok
Lee, Sang Hun
Kim, Dae Joong
Nam, Sang Yoon
Lee, Beom Jun
Lee, Hyun Jik
author_facet Seok, Ju Hyung
Kim, Dae Hyun
Kim, Hye Jih
Jo, Hang Hyo
Kim, Eun Young
Jeong, Jae-Hwang
Park, Young Seok
Lee, Sang Hun
Kim, Dae Joong
Nam, Sang Yoon
Lee, Beom Jun
Lee, Hyun Jik
author_sort Seok, Ju Hyung
collection PubMed
description BACKGROUND: Previous studies have presented evidence to support the significant association between red meat intake and colon cancer, suggesting that heme iron plays a key role in colon carcinogenesis. Epigallocatechin-3-gallate (EGCG), the major constituent of green tea, exhibits anti-oxidative and anti-cancer effects. However, the effect of EGCG on red meat-associated colon carcinogenesis is not well understood. OBJECTIVES: We aimed to investigate the regulatory effects of hemin and EGCG on colon carcinogenesis and the underlying mechanism of action. METHODS: Hemin and EGCG were treated in Caco2 cells to perform the water-soluble tetrazolium salt-1 assay, lactate dehydrogenase release assay, reactive oxygen species (ROS) detection assay, real-time quantitative polymerase chain reaction and western blot. We investigated the regulatory effects of hemin and EGCG on an azoxymethane (AOM) and dextran sodium sulfate (DSS)-induced colon carcinogenesis mouse model. RESULTS: In Caco2 cells, hemin increased cell proliferation and the expression of cell cycle regulatory proteins, and ROS levels. EGCG suppressed hemin-induced cell proliferation and cell cycle regulatory protein expression as well as mitochondrial ROS accumulation. Hemin increased nuclear factor erythroid-2-related factor 2 (Nrf2) expression, but decreased Keap1 expression. EGCG enhanced hemin-induced Nrf2 and antioxidant gene expression. Nrf2 inhibitor reversed EGCG reduced cell proliferation and cell cycle regulatory protein expression. In AOM/DSS mice, hemin treatment induced hyperplastic changes in colon tissues, inhibited by EGCG supplementation. EGCG reduced the hemin-induced numbers of total aberrant crypts and malondialdehyde concentration in the AOM/DSS model. CONCLUSIONS: We demonstrated that EGCG reduced hemin-induced proliferation and colon carcinogenesis through Nrf2-inhibited mitochondrial ROS accumulation.
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spelling pubmed-95233422022-10-11 Epigallocatechin-3-gallate suppresses hemin-aggravated colon carcinogenesis through Nrf2-inhibited mitochondrial reactive oxygen species accumulation Seok, Ju Hyung Kim, Dae Hyun Kim, Hye Jih Jo, Hang Hyo Kim, Eun Young Jeong, Jae-Hwang Park, Young Seok Lee, Sang Hun Kim, Dae Joong Nam, Sang Yoon Lee, Beom Jun Lee, Hyun Jik J Vet Sci Original Article BACKGROUND: Previous studies have presented evidence to support the significant association between red meat intake and colon cancer, suggesting that heme iron plays a key role in colon carcinogenesis. Epigallocatechin-3-gallate (EGCG), the major constituent of green tea, exhibits anti-oxidative and anti-cancer effects. However, the effect of EGCG on red meat-associated colon carcinogenesis is not well understood. OBJECTIVES: We aimed to investigate the regulatory effects of hemin and EGCG on colon carcinogenesis and the underlying mechanism of action. METHODS: Hemin and EGCG were treated in Caco2 cells to perform the water-soluble tetrazolium salt-1 assay, lactate dehydrogenase release assay, reactive oxygen species (ROS) detection assay, real-time quantitative polymerase chain reaction and western blot. We investigated the regulatory effects of hemin and EGCG on an azoxymethane (AOM) and dextran sodium sulfate (DSS)-induced colon carcinogenesis mouse model. RESULTS: In Caco2 cells, hemin increased cell proliferation and the expression of cell cycle regulatory proteins, and ROS levels. EGCG suppressed hemin-induced cell proliferation and cell cycle regulatory protein expression as well as mitochondrial ROS accumulation. Hemin increased nuclear factor erythroid-2-related factor 2 (Nrf2) expression, but decreased Keap1 expression. EGCG enhanced hemin-induced Nrf2 and antioxidant gene expression. Nrf2 inhibitor reversed EGCG reduced cell proliferation and cell cycle regulatory protein expression. In AOM/DSS mice, hemin treatment induced hyperplastic changes in colon tissues, inhibited by EGCG supplementation. EGCG reduced the hemin-induced numbers of total aberrant crypts and malondialdehyde concentration in the AOM/DSS model. CONCLUSIONS: We demonstrated that EGCG reduced hemin-induced proliferation and colon carcinogenesis through Nrf2-inhibited mitochondrial ROS accumulation. The Korean Society of Veterinary Science 2022-08-18 /pmc/articles/PMC9523342/ /pubmed/36174978 http://dx.doi.org/10.4142/jvs.22097 Text en © 2022 The Korean Society of Veterinary Science https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0 (https://creativecommons.org/licenses/by-nc/4.0/) ) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Seok, Ju Hyung
Kim, Dae Hyun
Kim, Hye Jih
Jo, Hang Hyo
Kim, Eun Young
Jeong, Jae-Hwang
Park, Young Seok
Lee, Sang Hun
Kim, Dae Joong
Nam, Sang Yoon
Lee, Beom Jun
Lee, Hyun Jik
Epigallocatechin-3-gallate suppresses hemin-aggravated colon carcinogenesis through Nrf2-inhibited mitochondrial reactive oxygen species accumulation
title Epigallocatechin-3-gallate suppresses hemin-aggravated colon carcinogenesis through Nrf2-inhibited mitochondrial reactive oxygen species accumulation
title_full Epigallocatechin-3-gallate suppresses hemin-aggravated colon carcinogenesis through Nrf2-inhibited mitochondrial reactive oxygen species accumulation
title_fullStr Epigallocatechin-3-gallate suppresses hemin-aggravated colon carcinogenesis through Nrf2-inhibited mitochondrial reactive oxygen species accumulation
title_full_unstemmed Epigallocatechin-3-gallate suppresses hemin-aggravated colon carcinogenesis through Nrf2-inhibited mitochondrial reactive oxygen species accumulation
title_short Epigallocatechin-3-gallate suppresses hemin-aggravated colon carcinogenesis through Nrf2-inhibited mitochondrial reactive oxygen species accumulation
title_sort epigallocatechin-3-gallate suppresses hemin-aggravated colon carcinogenesis through nrf2-inhibited mitochondrial reactive oxygen species accumulation
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9523342/
https://www.ncbi.nlm.nih.gov/pubmed/36174978
http://dx.doi.org/10.4142/jvs.22097
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