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Induction of SIRT1 by melatonin improves alcohol‐mediated oxidative liver injury by disrupting the CRBN‐YY1‐CYP2E1 signaling pathway
Alcoholic liver disease is the most prevalent chronic liver disease. Melatonin is known to control many vital processes. Here, we explored a novel molecular mechanism by which melatonin‐induced SIRT1 signaling protects against alcohol‐mediated oxidative stress and liver injury. Gene expression profi...
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Published in: | Journal of pineal research 2020-04, Vol.68 (3), p.e12638-n/a |
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creator | Lee, Sung‐Eun Koh, Hong Joo, Dong Jin Nedumaran, Balachandar Jeon, Hwang‐Ju Park, Chul‐Seung Harris, Robert A. Kim, Yong Deuk |
description | Alcoholic liver disease is the most prevalent chronic liver disease. Melatonin is known to control many vital processes. Here, we explored a novel molecular mechanism by which melatonin‐induced SIRT1 signaling protects against alcohol‐mediated oxidative stress and liver injury. Gene expression profiles and metabolic changes were measured in liver specimens of mice and human subjects. Expression levels of Cb1r, Crbn, Btg2, Yy1, pro‐inflammatory cytokines, and Cyp2e1 were significantly enhanced in chronic alcohol‐challenged mice and human subjects. Levels of serum alanine aminotransferase (ALT), aspartate aminotransferase (AST), hepatic CYP2E1 protein, and reactive oxygen species (ROS) were elevated in alcohol‐fed WT mice but not in Cb1r antagonist‐treated, Crbn null, or Yy1‐silenced mice. Importantly, alcohol‐induced Yy1 and Cyp2e1 expression, ROS amount, and liver injury were markedly diminished by melatonin treatment and the transduction of Sirt1 in mice, whereas this phenomenon was prominently ablated by silencing of Sirt1. Notably, SIRT1 physically interacted with YY1 and attenuated YY1 occupancy on the Cyp2e1 gene promoter. Melatonin‐SIRT1 signaling ameliorates alcohol‐induced oxidative liver injury by disrupting the CRBN‐YY1‐CYP2E1 signaling pathway. The manipulation of CRBN‐YY1‐CYP2E1 signaling network by the melatonin‐SIRT1 pathway highlights a novel entry point for treating alcoholic liver disease. |
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Melatonin is known to control many vital processes. Here, we explored a novel molecular mechanism by which melatonin‐induced SIRT1 signaling protects against alcohol‐mediated oxidative stress and liver injury. Gene expression profiles and metabolic changes were measured in liver specimens of mice and human subjects. Expression levels of Cb1r, Crbn, Btg2, Yy1, pro‐inflammatory cytokines, and Cyp2e1 were significantly enhanced in chronic alcohol‐challenged mice and human subjects. Levels of serum alanine aminotransferase (ALT), aspartate aminotransferase (AST), hepatic CYP2E1 protein, and reactive oxygen species (ROS) were elevated in alcohol‐fed WT mice but not in Cb1r antagonist‐treated, Crbn null, or Yy1‐silenced mice. Importantly, alcohol‐induced Yy1 and Cyp2e1 expression, ROS amount, and liver injury were markedly diminished by melatonin treatment and the transduction of Sirt1 in mice, whereas this phenomenon was prominently ablated by silencing of Sirt1. Notably, SIRT1 physically interacted with YY1 and attenuated YY1 occupancy on the Cyp2e1 gene promoter. Melatonin‐SIRT1 signaling ameliorates alcohol‐induced oxidative liver injury by disrupting the CRBN‐YY1‐CYP2E1 signaling pathway. The manipulation of CRBN‐YY1‐CYP2E1 signaling network by the melatonin‐SIRT1 pathway highlights a novel entry point for treating alcoholic liver disease.</description><identifier>ISSN: 0742-3098</identifier><identifier>EISSN: 1600-079X</identifier><identifier>DOI: 10.1111/jpi.12638</identifier><identifier>PMID: 32053237</identifier><language>eng</language><publisher>England</publisher><subject>Adaptor Proteins, Signal Transducing - metabolism ; alcoholic liver disease ; Animals ; Cytochrome P-450 CYP2E1 - metabolism ; cytochrome P450 2E1 ; Humans ; Liver Diseases, Alcoholic - metabolism ; melatonin ; Melatonin - metabolism ; metabolism ; Mice ; oxidative liver injury ; Oxidative Stress - physiology ; reactive oxygen species ; Signal Transduction - physiology ; Sirt1 ; Sirtuin 1 - metabolism ; Ubiquitin-Protein Ligases - metabolism ; YY1 Transcription Factor - metabolism</subject><ispartof>Journal of pineal research, 2020-04, Vol.68 (3), p.e12638-n/a</ispartof><rights>2020 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd</rights><rights>2020 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3258-2c0ef8f029509bd510b2bfffdafd0b8cfabe9bbe646fbe812e1b248a0aec89ca3</citedby><cites>FETCH-LOGICAL-c3258-2c0ef8f029509bd510b2bfffdafd0b8cfabe9bbe646fbe812e1b248a0aec89ca3</cites><orcidid>0000-0002-3330-6538 ; 0000-0001-8876-8353</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32053237$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lee, Sung‐Eun</creatorcontrib><creatorcontrib>Koh, Hong</creatorcontrib><creatorcontrib>Joo, Dong Jin</creatorcontrib><creatorcontrib>Nedumaran, Balachandar</creatorcontrib><creatorcontrib>Jeon, Hwang‐Ju</creatorcontrib><creatorcontrib>Park, Chul‐Seung</creatorcontrib><creatorcontrib>Harris, Robert A.</creatorcontrib><creatorcontrib>Kim, Yong Deuk</creatorcontrib><title>Induction of SIRT1 by melatonin improves alcohol‐mediated oxidative liver injury by disrupting the CRBN‐YY1‐CYP2E1 signaling pathway</title><title>Journal of pineal research</title><addtitle>J Pineal Res</addtitle><description>Alcoholic liver disease is the most prevalent chronic liver disease. Melatonin is known to control many vital processes. Here, we explored a novel molecular mechanism by which melatonin‐induced SIRT1 signaling protects against alcohol‐mediated oxidative stress and liver injury. Gene expression profiles and metabolic changes were measured in liver specimens of mice and human subjects. Expression levels of Cb1r, Crbn, Btg2, Yy1, pro‐inflammatory cytokines, and Cyp2e1 were significantly enhanced in chronic alcohol‐challenged mice and human subjects. Levels of serum alanine aminotransferase (ALT), aspartate aminotransferase (AST), hepatic CYP2E1 protein, and reactive oxygen species (ROS) were elevated in alcohol‐fed WT mice but not in Cb1r antagonist‐treated, Crbn null, or Yy1‐silenced mice. Importantly, alcohol‐induced Yy1 and Cyp2e1 expression, ROS amount, and liver injury were markedly diminished by melatonin treatment and the transduction of Sirt1 in mice, whereas this phenomenon was prominently ablated by silencing of Sirt1. Notably, SIRT1 physically interacted with YY1 and attenuated YY1 occupancy on the Cyp2e1 gene promoter. Melatonin‐SIRT1 signaling ameliorates alcohol‐induced oxidative liver injury by disrupting the CRBN‐YY1‐CYP2E1 signaling pathway. The manipulation of CRBN‐YY1‐CYP2E1 signaling network by the melatonin‐SIRT1 pathway highlights a novel entry point for treating alcoholic liver disease.</description><subject>Adaptor Proteins, Signal Transducing - metabolism</subject><subject>alcoholic liver disease</subject><subject>Animals</subject><subject>Cytochrome P-450 CYP2E1 - metabolism</subject><subject>cytochrome P450 2E1</subject><subject>Humans</subject><subject>Liver Diseases, Alcoholic - metabolism</subject><subject>melatonin</subject><subject>Melatonin - metabolism</subject><subject>metabolism</subject><subject>Mice</subject><subject>oxidative liver injury</subject><subject>Oxidative Stress - physiology</subject><subject>reactive oxygen species</subject><subject>Signal Transduction - physiology</subject><subject>Sirt1</subject><subject>Sirtuin 1 - metabolism</subject><subject>Ubiquitin-Protein Ligases - metabolism</subject><subject>YY1 Transcription Factor - metabolism</subject><issn>0742-3098</issn><issn>1600-079X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNp1kL1OwzAURi0EoqUw8ALIK0Paa6dJnRGqAkEVVKVIdIrsxG5d5U9O0pKNmYln5ElICbBxh3uX833SPQidE-iTZgabXPcJdW12gLrEBbBg5L0coi6MhtSywWMddFIUGwBgjLnHqGNTcGxqj7ro3U-jKix1luJM4Sd_viBY1DiRMS-zVKdYJ7nJtrLAPA6zdRZ_vn0kMtK8lBHOXnXES72VOG6WwTrdVKbe5yNdmCovdbrC5Vri8fz6oQkul6TZ4-WMTggu9Crl8Z7Iebne8foUHSkeF_Ls5_bQ881kMb6zpo-3_vhqaoU2dZhFQ5CKKaCeA56IHAKCCqVUxFUEgoWKC-kJId2hq4RkhEoi6JBx4DJkXsjtHrpse0OTFYWRKsiNTripAwLB3mfQ-Ay-fTbsRcvmlWje_iN_BTbAoAV2Opb1_03B_cxvK78AwfOFvQ</recordid><startdate>202004</startdate><enddate>202004</enddate><creator>Lee, Sung‐Eun</creator><creator>Koh, Hong</creator><creator>Joo, Dong Jin</creator><creator>Nedumaran, Balachandar</creator><creator>Jeon, Hwang‐Ju</creator><creator>Park, Chul‐Seung</creator><creator>Harris, Robert A.</creator><creator>Kim, Yong Deuk</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><orcidid>https://orcid.org/0000-0002-3330-6538</orcidid><orcidid>https://orcid.org/0000-0001-8876-8353</orcidid></search><sort><creationdate>202004</creationdate><title>Induction of SIRT1 by melatonin improves alcohol‐mediated oxidative liver injury by disrupting the CRBN‐YY1‐CYP2E1 signaling pathway</title><author>Lee, Sung‐Eun ; Koh, Hong ; Joo, Dong Jin ; Nedumaran, Balachandar ; Jeon, Hwang‐Ju ; Park, Chul‐Seung ; Harris, Robert A. ; Kim, Yong Deuk</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3258-2c0ef8f029509bd510b2bfffdafd0b8cfabe9bbe646fbe812e1b248a0aec89ca3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Adaptor Proteins, Signal Transducing - metabolism</topic><topic>alcoholic liver disease</topic><topic>Animals</topic><topic>Cytochrome P-450 CYP2E1 - metabolism</topic><topic>cytochrome P450 2E1</topic><topic>Humans</topic><topic>Liver Diseases, Alcoholic - metabolism</topic><topic>melatonin</topic><topic>Melatonin - metabolism</topic><topic>metabolism</topic><topic>Mice</topic><topic>oxidative liver injury</topic><topic>Oxidative Stress - physiology</topic><topic>reactive oxygen species</topic><topic>Signal Transduction - physiology</topic><topic>Sirt1</topic><topic>Sirtuin 1 - metabolism</topic><topic>Ubiquitin-Protein Ligases - metabolism</topic><topic>YY1 Transcription Factor - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lee, Sung‐Eun</creatorcontrib><creatorcontrib>Koh, Hong</creatorcontrib><creatorcontrib>Joo, Dong Jin</creatorcontrib><creatorcontrib>Nedumaran, Balachandar</creatorcontrib><creatorcontrib>Jeon, Hwang‐Ju</creatorcontrib><creatorcontrib>Park, Chul‐Seung</creatorcontrib><creatorcontrib>Harris, Robert A.</creatorcontrib><creatorcontrib>Kim, Yong Deuk</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>Journal of pineal research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lee, Sung‐Eun</au><au>Koh, Hong</au><au>Joo, Dong Jin</au><au>Nedumaran, Balachandar</au><au>Jeon, Hwang‐Ju</au><au>Park, Chul‐Seung</au><au>Harris, Robert A.</au><au>Kim, Yong Deuk</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Induction of SIRT1 by melatonin improves alcohol‐mediated oxidative liver injury by disrupting the CRBN‐YY1‐CYP2E1 signaling pathway</atitle><jtitle>Journal of pineal research</jtitle><addtitle>J Pineal Res</addtitle><date>2020-04</date><risdate>2020</risdate><volume>68</volume><issue>3</issue><spage>e12638</spage><epage>n/a</epage><pages>e12638-n/a</pages><issn>0742-3098</issn><eissn>1600-079X</eissn><abstract>Alcoholic liver disease is the most prevalent chronic liver disease. Melatonin is known to control many vital processes. Here, we explored a novel molecular mechanism by which melatonin‐induced SIRT1 signaling protects against alcohol‐mediated oxidative stress and liver injury. Gene expression profiles and metabolic changes were measured in liver specimens of mice and human subjects. Expression levels of Cb1r, Crbn, Btg2, Yy1, pro‐inflammatory cytokines, and Cyp2e1 were significantly enhanced in chronic alcohol‐challenged mice and human subjects. Levels of serum alanine aminotransferase (ALT), aspartate aminotransferase (AST), hepatic CYP2E1 protein, and reactive oxygen species (ROS) were elevated in alcohol‐fed WT mice but not in Cb1r antagonist‐treated, Crbn null, or Yy1‐silenced mice. Importantly, alcohol‐induced Yy1 and Cyp2e1 expression, ROS amount, and liver injury were markedly diminished by melatonin treatment and the transduction of Sirt1 in mice, whereas this phenomenon was prominently ablated by silencing of Sirt1. Notably, SIRT1 physically interacted with YY1 and attenuated YY1 occupancy on the Cyp2e1 gene promoter. Melatonin‐SIRT1 signaling ameliorates alcohol‐induced oxidative liver injury by disrupting the CRBN‐YY1‐CYP2E1 signaling pathway. The manipulation of CRBN‐YY1‐CYP2E1 signaling network by the melatonin‐SIRT1 pathway highlights a novel entry point for treating alcoholic liver disease.</abstract><cop>England</cop><pmid>32053237</pmid><doi>10.1111/jpi.12638</doi><tpages>15</tpages><orcidid>https://orcid.org/0000-0002-3330-6538</orcidid><orcidid>https://orcid.org/0000-0001-8876-8353</orcidid></addata></record> |
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subjects | Adaptor Proteins, Signal Transducing - metabolism alcoholic liver disease Animals Cytochrome P-450 CYP2E1 - metabolism cytochrome P450 2E1 Humans Liver Diseases, Alcoholic - metabolism melatonin Melatonin - metabolism metabolism Mice oxidative liver injury Oxidative Stress - physiology reactive oxygen species Signal Transduction - physiology Sirt1 Sirtuin 1 - metabolism Ubiquitin-Protein Ligases - metabolism YY1 Transcription Factor - metabolism |
title | Induction of SIRT1 by melatonin improves alcohol‐mediated oxidative liver injury by disrupting the CRBN‐YY1‐CYP2E1 signaling pathway |
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