MicroRNA 125a-5p Inhibits Cell Proliferation and Induces Apoptosis in Hepatitis B Virus-Related Hepatocellular Carcinoma by Downregulation of ErbB3
MicroRNAs, a class of endogenous noncoding RNAs, regulate gene expression at the posttranscriptional level and thus take part in multiple biological processes. An increasing number of miRNAs have been found to be dysregulated in hepatocellular carcinoma (HCC) and are involved in liver tumorigenesis....
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Veröffentlicht in: | Oncology research 2019-03, Vol.27 (4), p.449-458 |
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description | MicroRNAs, a class of endogenous noncoding RNAs, regulate gene expression at the posttranscriptional level and thus take part in multiple biological processes. An increasing number of miRNAs have been found to be dysregulated in hepatocellular carcinoma (HCC) and are involved in liver
tumorigenesis. In this study, miR-125a-5p was found to be obviously downregulated much more in hepatitis B virus (HBV)-related HCC. To investigate the effects of miR-125a-5p, miR-125a-5p was overexpressed in HepG2.2.15 and HepG3X cells. The findings have indicated that overexpression of miR-125a-5p
dramatically inhibited cell proliferation and induced cell apoptosis. Furthermore, overexpression of miR-125a-5p could significantly decrease the secretion of HBsAg and HBeAg. In concordance to this, the expression of ErbB3 was upregulated in human HBV-related HCC tissue, HepG2.2.15 cells,
and HepG3X cells. miR-125a-5p directly targeted ErbB3 and reduced both mRNA and protein levels of ErbB3, which promoted cell proliferation and suppressed cell apoptosis in HCC cells. Our results provide new insights into the function of miR-125a-5p in HBV-related HCC. It is beneficial to gain
insight into the mechanism of HBV infection and pathophysiology of HBV-related HCC. |
doi_str_mv | 10.3727/096504017X15016337254623 |
format | Article |
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tumorigenesis. In this study, miR-125a-5p was found to be obviously downregulated much more in hepatitis B virus (HBV)-related HCC. To investigate the effects of miR-125a-5p, miR-125a-5p was overexpressed in HepG2.2.15 and HepG3X cells. The findings have indicated that overexpression of miR-125a-5p
dramatically inhibited cell proliferation and induced cell apoptosis. Furthermore, overexpression of miR-125a-5p could significantly decrease the secretion of HBsAg and HBeAg. In concordance to this, the expression of ErbB3 was upregulated in human HBV-related HCC tissue, HepG2.2.15 cells,
and HepG3X cells. miR-125a-5p directly targeted ErbB3 and reduced both mRNA and protein levels of ErbB3, which promoted cell proliferation and suppressed cell apoptosis in HCC cells. Our results provide new insights into the function of miR-125a-5p in HBV-related HCC. It is beneficial to gain
insight into the mechanism of HBV infection and pathophysiology of HBV-related HCC.</description><identifier>ISSN: 0965-0407</identifier><identifier>EISSN: 1555-3906</identifier><identifier>DOI: 10.3727/096504017X15016337254623</identifier><identifier>PMID: 28800792</identifier><language>eng</language><publisher>Elmsford, NY: Cognizant Communication Corporation</publisher><subject>Apoptosis ; Apoptosis - genetics ; Carcinoma, Hepatocellular - etiology ; Caspase 3 - metabolism ; Cell Proliferation ; Cell Survival ; Erbb3 ; Gene Expression Regulation, Neoplastic ; Hepatitis B - complications ; Hepatitis B - virology ; Hepatitis B Virus (hbv) ; Hepatocellular Carcinoma (hcc) ; Humans ; Liver Neoplasms - etiology ; MicroRNAs - genetics ; Mir-125a-5p ; Proliferation ; Receptor, ErbB-3 - genetics ; RNA Interference</subject><ispartof>Oncology research, 2019-03, Vol.27 (4), p.449-458</ispartof><rights>Copyright © 2019 Cognizant, LLC. 2019</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c666t-618c87e4eff8e90c24da08cce660b1f251bfa163d791728ac3e12b2aaf8313e3</citedby><cites>FETCH-LOGICAL-c666t-618c87e4eff8e90c24da08cce660b1f251bfa163d791728ac3e12b2aaf8313e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7848293/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7848293/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,288,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28800792$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Li, Guoyun</creatorcontrib><creatorcontrib>Zhang, Wei</creatorcontrib><creatorcontrib>Gong, Li</creatorcontrib><creatorcontrib>Huang, Xiaoping</creatorcontrib><title>MicroRNA 125a-5p Inhibits Cell Proliferation and Induces Apoptosis in Hepatitis B Virus-Related Hepatocellular Carcinoma by Downregulation of ErbB3</title><title>Oncology research</title><addtitle>Oncol Res</addtitle><description>MicroRNAs, a class of endogenous noncoding RNAs, regulate gene expression at the posttranscriptional level and thus take part in multiple biological processes. An increasing number of miRNAs have been found to be dysregulated in hepatocellular carcinoma (HCC) and are involved in liver
tumorigenesis. In this study, miR-125a-5p was found to be obviously downregulated much more in hepatitis B virus (HBV)-related HCC. To investigate the effects of miR-125a-5p, miR-125a-5p was overexpressed in HepG2.2.15 and HepG3X cells. The findings have indicated that overexpression of miR-125a-5p
dramatically inhibited cell proliferation and induced cell apoptosis. Furthermore, overexpression of miR-125a-5p could significantly decrease the secretion of HBsAg and HBeAg. In concordance to this, the expression of ErbB3 was upregulated in human HBV-related HCC tissue, HepG2.2.15 cells,
and HepG3X cells. miR-125a-5p directly targeted ErbB3 and reduced both mRNA and protein levels of ErbB3, which promoted cell proliferation and suppressed cell apoptosis in HCC cells. Our results provide new insights into the function of miR-125a-5p in HBV-related HCC. It is beneficial to gain
insight into the mechanism of HBV infection and pathophysiology of HBV-related HCC.</description><subject>Apoptosis</subject><subject>Apoptosis - genetics</subject><subject>Carcinoma, Hepatocellular - etiology</subject><subject>Caspase 3 - metabolism</subject><subject>Cell Proliferation</subject><subject>Cell Survival</subject><subject>Erbb3</subject><subject>Gene Expression Regulation, Neoplastic</subject><subject>Hepatitis B - complications</subject><subject>Hepatitis B - virology</subject><subject>Hepatitis B Virus (hbv)</subject><subject>Hepatocellular Carcinoma (hcc)</subject><subject>Humans</subject><subject>Liver Neoplasms - etiology</subject><subject>MicroRNAs - genetics</subject><subject>Mir-125a-5p</subject><subject>Proliferation</subject><subject>Receptor, ErbB-3 - genetics</subject><subject>RNA Interference</subject><issn>0965-0407</issn><issn>1555-3906</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kdtu1DAQhiMEokvhFZAvuQn4EMfODdJ2KbRSC6iqEHfWxHG2rrJ2sJ2i8hq8MM6mLSCEb3yYf74Z_1MUiODXTFDxBjc1xxUm4ivhmNQsP_KqpuxRsSKc85I1uH5crGZZmXXioHgW4zXGtBJV87Q4oFJiLBq6Kn6eWx38xcc1IpRDyUd06q5sa1NEGzMM6HPwg-1NgGS9Q-C6HO8mbSJaj35MPtqIrEMnZsyKlC9H6IsNUywvzADJdEvE68yaBghoA0Fb53eA2lv0zn93wWxzYE_3PToO7RF7XjzpYYjmxd1-WFy-P77cnJRnnz6cbtZnpa7rOpU1kVoKU5m-l6bBmlYdYKm1qWvckp5y0vaQzelEQwSVoJkhtKUAvWSEGXZYvF2w49TuTKeNSwEGNQa7g3CrPFj1d8TZK7X1N0rIStKGZcCrO0Dw3yYTk9rZOP8UnPFTVKShkhMm9lK5SLPZMQbTP5QhWM0jVf8baU59-WebD4n3M8yC80Vg3TZ3CuraT8Fl45TVSvvtPVqoGypcpSimBMtcl2AuVWd6mIakEgS1_aGi-O3LP7wZ5kMGkEbh_ZobX1alIKT5INgvDa7MEA</recordid><startdate>20190329</startdate><enddate>20190329</enddate><creator>Li, Guoyun</creator><creator>Zhang, Wei</creator><creator>Gong, Li</creator><creator>Huang, Xiaoping</creator><general>Cognizant Communication Corporation</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20190329</creationdate><title>MicroRNA 125a-5p Inhibits Cell Proliferation and Induces Apoptosis in Hepatitis B Virus-Related Hepatocellular Carcinoma by Downregulation of ErbB3</title><author>Li, Guoyun ; Zhang, Wei ; Gong, Li ; Huang, Xiaoping</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c666t-618c87e4eff8e90c24da08cce660b1f251bfa163d791728ac3e12b2aaf8313e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Apoptosis</topic><topic>Apoptosis - genetics</topic><topic>Carcinoma, Hepatocellular - etiology</topic><topic>Caspase 3 - metabolism</topic><topic>Cell Proliferation</topic><topic>Cell Survival</topic><topic>Erbb3</topic><topic>Gene Expression Regulation, Neoplastic</topic><topic>Hepatitis B - complications</topic><topic>Hepatitis B - virology</topic><topic>Hepatitis B Virus (hbv)</topic><topic>Hepatocellular Carcinoma (hcc)</topic><topic>Humans</topic><topic>Liver Neoplasms - etiology</topic><topic>MicroRNAs - genetics</topic><topic>Mir-125a-5p</topic><topic>Proliferation</topic><topic>Receptor, ErbB-3 - genetics</topic><topic>RNA Interference</topic><toplevel>online_resources</toplevel><creatorcontrib>Li, Guoyun</creatorcontrib><creatorcontrib>Zhang, Wei</creatorcontrib><creatorcontrib>Gong, Li</creatorcontrib><creatorcontrib>Huang, Xiaoping</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Oncology research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Li, Guoyun</au><au>Zhang, Wei</au><au>Gong, Li</au><au>Huang, Xiaoping</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>MicroRNA 125a-5p Inhibits Cell Proliferation and Induces Apoptosis in Hepatitis B Virus-Related Hepatocellular Carcinoma by Downregulation of ErbB3</atitle><jtitle>Oncology research</jtitle><addtitle>Oncol Res</addtitle><date>2019-03-29</date><risdate>2019</risdate><volume>27</volume><issue>4</issue><spage>449</spage><epage>458</epage><pages>449-458</pages><issn>0965-0407</issn><eissn>1555-3906</eissn><abstract>MicroRNAs, a class of endogenous noncoding RNAs, regulate gene expression at the posttranscriptional level and thus take part in multiple biological processes. An increasing number of miRNAs have been found to be dysregulated in hepatocellular carcinoma (HCC) and are involved in liver
tumorigenesis. In this study, miR-125a-5p was found to be obviously downregulated much more in hepatitis B virus (HBV)-related HCC. To investigate the effects of miR-125a-5p, miR-125a-5p was overexpressed in HepG2.2.15 and HepG3X cells. The findings have indicated that overexpression of miR-125a-5p
dramatically inhibited cell proliferation and induced cell apoptosis. Furthermore, overexpression of miR-125a-5p could significantly decrease the secretion of HBsAg and HBeAg. In concordance to this, the expression of ErbB3 was upregulated in human HBV-related HCC tissue, HepG2.2.15 cells,
and HepG3X cells. miR-125a-5p directly targeted ErbB3 and reduced both mRNA and protein levels of ErbB3, which promoted cell proliferation and suppressed cell apoptosis in HCC cells. Our results provide new insights into the function of miR-125a-5p in HBV-related HCC. It is beneficial to gain
insight into the mechanism of HBV infection and pathophysiology of HBV-related HCC.</abstract><cop>Elmsford, NY</cop><pub>Cognizant Communication Corporation</pub><pmid>28800792</pmid><doi>10.3727/096504017X15016337254623</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Apoptosis Apoptosis - genetics Carcinoma, Hepatocellular - etiology Caspase 3 - metabolism Cell Proliferation Cell Survival Erbb3 Gene Expression Regulation, Neoplastic Hepatitis B - complications Hepatitis B - virology Hepatitis B Virus (hbv) Hepatocellular Carcinoma (hcc) Humans Liver Neoplasms - etiology MicroRNAs - genetics Mir-125a-5p Proliferation Receptor, ErbB-3 - genetics RNA Interference |
title | MicroRNA 125a-5p Inhibits Cell Proliferation and Induces Apoptosis in Hepatitis B Virus-Related Hepatocellular Carcinoma by Downregulation of ErbB3 |
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