IFITM3 upregulates c-myc expression to promote hepatocellular carcinoma proliferation via the ERK1/2 signalling pathway
Interferon-induced transmembrane protein 3 (IFITM3) is associated with cancer development. Proto-oncogene c-myc can promote tumor proliferation. However, collections of IFITM3 and c-myc in hepatocellular carcinoma (HCC) and the potential role and mechanisms of IFITM3 in c-myc-mediated tumor prolifer...
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Veröffentlicht in: | BioScience Trends 2019/12/31, Vol.13(6), pp.523-529 |
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description | Interferon-induced transmembrane protein 3 (IFITM3) is associated with cancer development. Proto-oncogene c-myc can promote tumor proliferation. However, collections of IFITM3 and c-myc in hepatocellular carcinoma (HCC) and the potential role and mechanisms of IFITM3 in c-myc-mediated tumor proliferation remain unclear. In this study, we investigated a positive correlation between the expression of IFITM3 and c-myc in HCC. The down-regulation of IFITM3 significantly reduced c-myc expression and inhibited the proliferation of HCC in vitro and in vivo. In addition, upregulated c-myc expression restored the decrease in cell proliferation caused by the downregulation of IFITM3, while downregulation of c-myc reduced the proliferation of HCC enhanced by IFITM3. Mechanistically, IFITM3 regulates c-myc expression via the ERK1/2 signalling pathway. In conclusion, a novel path of IFITM3–ERK1/2–c-myc regulatory circuitry was identified, and its dysfunction may lead to HCC tumorigenesis. |
doi_str_mv | 10.5582/bst.2019.01289 |
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Proto-oncogene c-myc can promote tumor proliferation. However, collections of IFITM3 and c-myc in hepatocellular carcinoma (HCC) and the potential role and mechanisms of IFITM3 in c-myc-mediated tumor proliferation remain unclear. In this study, we investigated a positive correlation between the expression of IFITM3 and c-myc in HCC. The down-regulation of IFITM3 significantly reduced c-myc expression and inhibited the proliferation of HCC in vitro and in vivo. In addition, upregulated c-myc expression restored the decrease in cell proliferation caused by the downregulation of IFITM3, while downregulation of c-myc reduced the proliferation of HCC enhanced by IFITM3. Mechanistically, IFITM3 regulates c-myc expression via the ERK1/2 signalling pathway. In conclusion, a novel path of IFITM3–ERK1/2–c-myc regulatory circuitry was identified, and its dysfunction may lead to HCC tumorigenesis.</description><identifier>ISSN: 1881-7815</identifier><identifier>EISSN: 1881-7823</identifier><identifier>DOI: 10.5582/bst.2019.01289</identifier><identifier>PMID: 31852866</identifier><language>eng</language><publisher>Japan: International Research and Cooperation Association for Bio & Socio-Sciences Advancement</publisher><subject>c-myc ; ERK1/2 signalling pathway ; hepatocellular carcinoma ; IFITM3 ; proliferation</subject><ispartof>BioScience Trends, 2019/12/31, Vol.13(6), pp.523-529</ispartof><rights>2019 International Research and Cooperation Association for Bio & Socio-Sciences Advancement</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c486t-e3c707230610112877e8f67a8d91c442512456d55598b8e48e56930e4d86a3853</citedby><cites>FETCH-LOGICAL-c486t-e3c707230610112877e8f67a8d91c442512456d55598b8e48e56930e4d86a3853</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,1876,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31852866$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Min, Jiaqi</creatorcontrib><creatorcontrib>Hu, Junwen</creatorcontrib><creatorcontrib>Luo, Chen</creatorcontrib><creatorcontrib>Zhu, Jinfeng</creatorcontrib><creatorcontrib>Zhao, Jiefeng</creatorcontrib><creatorcontrib>Zhu, Zhengming</creatorcontrib><creatorcontrib>Wu, Linquan</creatorcontrib><creatorcontrib>Yuan, Rongfa</creatorcontrib><title>IFITM3 upregulates c-myc expression to promote hepatocellular carcinoma proliferation via the ERK1/2 signalling pathway</title><title>BioScience Trends</title><addtitle>BST</addtitle><description>Interferon-induced transmembrane protein 3 (IFITM3) is associated with cancer development. Proto-oncogene c-myc can promote tumor proliferation. However, collections of IFITM3 and c-myc in hepatocellular carcinoma (HCC) and the potential role and mechanisms of IFITM3 in c-myc-mediated tumor proliferation remain unclear. In this study, we investigated a positive correlation between the expression of IFITM3 and c-myc in HCC. The down-regulation of IFITM3 significantly reduced c-myc expression and inhibited the proliferation of HCC in vitro and in vivo. In addition, upregulated c-myc expression restored the decrease in cell proliferation caused by the downregulation of IFITM3, while downregulation of c-myc reduced the proliferation of HCC enhanced by IFITM3. Mechanistically, IFITM3 regulates c-myc expression via the ERK1/2 signalling pathway. In conclusion, a novel path of IFITM3–ERK1/2–c-myc regulatory circuitry was identified, and its dysfunction may lead to HCC tumorigenesis.</description><subject>c-myc</subject><subject>ERK1/2 signalling pathway</subject><subject>hepatocellular carcinoma</subject><subject>IFITM3</subject><subject>proliferation</subject><issn>1881-7815</issn><issn>1881-7823</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNpFkEtPAyEURonRqFG3Lg1LN1N5DAyzNLXVRo2J0TWh9LalmUcFxtp_L2O1soAbOPfL5SB0SclACMVupiEOGKHlgFCmygN0SpWiWaEYP9zXVJygixBWJC0hqSrkMTrhVAmmpDxFm8l48vbMcbf2sOgqEyFgm9Vbi-ErXYXg2gbHFq99W7cR8BLWJrYWqirBHlvjrWva2vRA5ebgTew7Pp3BcQl49PpIbxgObtGYqnLNAqf25cZsz9HR3FQBLn7PM_Q-Hr0NH7Knl_vJ8PYps7mSMQNuC1IwTiQlNH2yKEDNZWHUrKQ2z5mgLBdyJoQo1VRBrkDIkhPIZ0oargQ_Q9e73DTfRwch6tqFfnzTQNsFzXgKlclMntDBDrW-DcHDXK-9q43fakp071sn37r3rX98p4ar3-xuWsNsj__ZTcDdDliFaBawB4yPzlbwk0e5lv32n7t_tkvjNTT8G-61kyE</recordid><startdate>20191231</startdate><enddate>20191231</enddate><creator>Min, Jiaqi</creator><creator>Hu, Junwen</creator><creator>Luo, Chen</creator><creator>Zhu, Jinfeng</creator><creator>Zhao, Jiefeng</creator><creator>Zhu, Zhengming</creator><creator>Wu, Linquan</creator><creator>Yuan, Rongfa</creator><general>International Research and Cooperation Association for Bio & Socio-Sciences Advancement</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20191231</creationdate><title>IFITM3 upregulates c-myc expression to promote hepatocellular carcinoma proliferation via the ERK1/2 signalling pathway</title><author>Min, Jiaqi ; Hu, Junwen ; Luo, Chen ; Zhu, Jinfeng ; Zhao, Jiefeng ; Zhu, Zhengming ; Wu, Linquan ; Yuan, Rongfa</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c486t-e3c707230610112877e8f67a8d91c442512456d55598b8e48e56930e4d86a3853</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>c-myc</topic><topic>ERK1/2 signalling pathway</topic><topic>hepatocellular carcinoma</topic><topic>IFITM3</topic><topic>proliferation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Min, Jiaqi</creatorcontrib><creatorcontrib>Hu, Junwen</creatorcontrib><creatorcontrib>Luo, Chen</creatorcontrib><creatorcontrib>Zhu, Jinfeng</creatorcontrib><creatorcontrib>Zhao, Jiefeng</creatorcontrib><creatorcontrib>Zhu, Zhengming</creatorcontrib><creatorcontrib>Wu, Linquan</creatorcontrib><creatorcontrib>Yuan, Rongfa</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>BioScience Trends</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Min, Jiaqi</au><au>Hu, Junwen</au><au>Luo, Chen</au><au>Zhu, Jinfeng</au><au>Zhao, Jiefeng</au><au>Zhu, Zhengming</au><au>Wu, Linquan</au><au>Yuan, Rongfa</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>IFITM3 upregulates c-myc expression to promote hepatocellular carcinoma proliferation via the ERK1/2 signalling pathway</atitle><jtitle>BioScience Trends</jtitle><addtitle>BST</addtitle><date>2019-12-31</date><risdate>2019</risdate><volume>13</volume><issue>6</issue><spage>523</spage><epage>529</epage><pages>523-529</pages><issn>1881-7815</issn><eissn>1881-7823</eissn><abstract>Interferon-induced transmembrane protein 3 (IFITM3) is associated with cancer development. Proto-oncogene c-myc can promote tumor proliferation. However, collections of IFITM3 and c-myc in hepatocellular carcinoma (HCC) and the potential role and mechanisms of IFITM3 in c-myc-mediated tumor proliferation remain unclear. In this study, we investigated a positive correlation between the expression of IFITM3 and c-myc in HCC. The down-regulation of IFITM3 significantly reduced c-myc expression and inhibited the proliferation of HCC in vitro and in vivo. In addition, upregulated c-myc expression restored the decrease in cell proliferation caused by the downregulation of IFITM3, while downregulation of c-myc reduced the proliferation of HCC enhanced by IFITM3. Mechanistically, IFITM3 regulates c-myc expression via the ERK1/2 signalling pathway. In conclusion, a novel path of IFITM3–ERK1/2–c-myc regulatory circuitry was identified, and its dysfunction may lead to HCC tumorigenesis.</abstract><cop>Japan</cop><pub>International Research and Cooperation Association for Bio & Socio-Sciences Advancement</pub><pmid>31852866</pmid><doi>10.5582/bst.2019.01289</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | c-myc ERK1/2 signalling pathway hepatocellular carcinoma IFITM3 proliferation |
title | IFITM3 upregulates c-myc expression to promote hepatocellular carcinoma proliferation via the ERK1/2 signalling pathway |
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