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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Veröffentlicht in: | Journal of veterinary science (Suwŏn-si, Korea) Korea), 2022, Vol.23 (5), p.74.1-74.16 |
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creator | 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 |
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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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.</description><identifier>ISSN: 1229-845X</identifier><identifier>EISSN: 1976-555X</identifier><language>kor</language><ispartof>Journal of veterinary science (Suwŏn-si, Korea), 2022, Vol.23 (5), p.74.1-74.16</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,315,781,785,886,4025</link.rule.ids></links><search><creatorcontrib>Seok, Ju Hyung</creatorcontrib><creatorcontrib>Kim, Dae Hyun</creatorcontrib><creatorcontrib>Kim, Hye Jih</creatorcontrib><creatorcontrib>Jo, Hang Hyo</creatorcontrib><creatorcontrib>Kim, Eun Young</creatorcontrib><creatorcontrib>Jeong, Jae-Hwang</creatorcontrib><creatorcontrib>Park, Young Seok</creatorcontrib><creatorcontrib>Lee, Sang Hun</creatorcontrib><creatorcontrib>Kim, Dae Joong</creatorcontrib><creatorcontrib>Nam, Sang Yoon</creatorcontrib><creatorcontrib>Lee, Beom Jun</creatorcontrib><creatorcontrib>Lee, Hyun Jik</creatorcontrib><title>Epigallocatechin-3-gallate suppresses hemin-aggravated colon carcinogenesis through Nrf2-inhibited mitochondrial reactive oxygen species accumulation</title><title>Journal of veterinary science (Suwŏn-si, Korea)</title><addtitle>Journal of veterinary science</addtitle><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.</description><issn>1229-845X</issn><issn>1976-555X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>JDI</sourceid><recordid>eNqNjcFKAzEYhIMoWLTvkIvHwDbbbLZHkYoo6KWH3kr6b5r8mE2W_NmiD-L7moIP4Glm-GaYK7ZYbXQnlFL76-ql3Ih-rfa3bEmEx0a1re563S_Yz3ZCZ0JIYIoFj1G04pJr4jRPU7ZElri3Y0XGuWzOFQ0cUkiRg8mAMTkbLSHx4nOanefv-SQFRo9HvHRHLAl8ikNGE3i2BgqeLU9f33XIabKA9cIAzONcjzHFe3ZzMoHs8k_v2MPzdvf0Ij6RCh7iQOHw-vj2IRsppdZKrTot1037394vp9VbPQ</recordid><startdate>2022</startdate><enddate>2022</enddate><creator>Seok, Ju Hyung</creator><creator>Kim, Dae Hyun</creator><creator>Kim, Hye Jih</creator><creator>Jo, Hang Hyo</creator><creator>Kim, Eun Young</creator><creator>Jeong, Jae-Hwang</creator><creator>Park, Young Seok</creator><creator>Lee, Sang Hun</creator><creator>Kim, Dae Joong</creator><creator>Nam, Sang Yoon</creator><creator>Lee, Beom Jun</creator><creator>Lee, Hyun Jik</creator><scope>JDI</scope></search><sort><creationdate>2022</creationdate><title>Epigallocatechin-3-gallate suppresses hemin-aggravated colon carcinogenesis through Nrf2-inhibited mitochondrial reactive oxygen species accumulation</title><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></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-kisti_ndsl_JAKO2022277551672403</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>kor</language><creationdate>2022</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Seok, Ju Hyung</creatorcontrib><creatorcontrib>Kim, Dae Hyun</creatorcontrib><creatorcontrib>Kim, Hye Jih</creatorcontrib><creatorcontrib>Jo, Hang Hyo</creatorcontrib><creatorcontrib>Kim, Eun Young</creatorcontrib><creatorcontrib>Jeong, Jae-Hwang</creatorcontrib><creatorcontrib>Park, Young Seok</creatorcontrib><creatorcontrib>Lee, Sang Hun</creatorcontrib><creatorcontrib>Kim, Dae Joong</creatorcontrib><creatorcontrib>Nam, Sang Yoon</creatorcontrib><creatorcontrib>Lee, Beom Jun</creatorcontrib><creatorcontrib>Lee, Hyun Jik</creatorcontrib><collection>KoreaScience</collection><jtitle>Journal of veterinary science (Suwŏn-si, Korea)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Seok, Ju Hyung</au><au>Kim, Dae Hyun</au><au>Kim, Hye Jih</au><au>Jo, Hang Hyo</au><au>Kim, Eun Young</au><au>Jeong, Jae-Hwang</au><au>Park, Young Seok</au><au>Lee, Sang Hun</au><au>Kim, Dae Joong</au><au>Nam, Sang Yoon</au><au>Lee, Beom Jun</au><au>Lee, Hyun Jik</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Epigallocatechin-3-gallate suppresses hemin-aggravated colon carcinogenesis through Nrf2-inhibited mitochondrial reactive oxygen species accumulation</atitle><jtitle>Journal of veterinary science (Suwŏn-si, Korea)</jtitle><addtitle>Journal of veterinary science</addtitle><date>2022</date><risdate>2022</risdate><volume>23</volume><issue>5</issue><spage>74.1</spage><epage>74.16</epage><pages>74.1-74.16</pages><issn>1229-845X</issn><eissn>1976-555X</eissn><abstract>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.</abstract><oa>free_for_read</oa></addata></record> |
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title | Epigallocatechin-3-gallate suppresses hemin-aggravated colon carcinogenesis through Nrf2-inhibited mitochondrial reactive oxygen species accumulation |
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