expression of HCV-associated host factors is dependent on the hepatoma cell line used in HCV studies
Chronic infection by hepatitis C virus (HCV) is a major cause of liver cirrhosis and hepatocellular carcinoma. At present, the most commonly used in vitro model of HCV infection is based on hepatoma cell lines. However, they were obtained from different patients and different cancers and/or differ i...
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Veröffentlicht in: | Archives of virology 2014-03, Vol.159 (3), p.527-534 |
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description | Chronic infection by hepatitis C virus (HCV) is a major cause of liver cirrhosis and hepatocellular carcinoma. At present, the most commonly used in vitro model of HCV infection is based on hepatoma cell lines. However, they were obtained from different patients and different cancers and/or differ in their characteristics and permissiveness to HCV. HCV infection can be modulated by several host factors, so we compared six different hepatoma cell lines that are used as in vitro models for HCV for some of these host factors: the seven known HCV entry factors, the six best-characterized HCV-associated microRNAs, and the two single-nucleotide polymorphisms near the IL28B gene associated with response to pegylated alpha interferon and ribavirin combination therapy, all assessed by quantitative PCR. We showed that the cell lines, including Huh-7 and Huh-7-derived cells, have different microRNA and HCV entry factor expression profiles as well as different IL28B genotypes. In conclusion, some of the observed differences might explain the differences in permissiveness of the cell lines, but, above all, they raise questions about the reliability of in vitro HCV research data gathered to date. |
doi_str_mv | 10.1007/s00705-013-1862-9 |
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At present, the most commonly used in vitro model of HCV infection is based on hepatoma cell lines. However, they were obtained from different patients and different cancers and/or differ in their characteristics and permissiveness to HCV. HCV infection can be modulated by several host factors, so we compared six different hepatoma cell lines that are used as in vitro models for HCV for some of these host factors: the seven known HCV entry factors, the six best-characterized HCV-associated microRNAs, and the two single-nucleotide polymorphisms near the IL28B gene associated with response to pegylated alpha interferon and ribavirin combination therapy, all assessed by quantitative PCR. We showed that the cell lines, including Huh-7 and Huh-7-derived cells, have different microRNA and HCV entry factor expression profiles as well as different IL28B genotypes. In conclusion, some of the observed differences might explain the differences in permissiveness of the cell lines, but, above all, they raise questions about the reliability of in vitro HCV research data gathered to date.</description><identifier>ISSN: 0304-8608</identifier><identifier>EISSN: 1432-8798</identifier><identifier>DOI: 10.1007/s00705-013-1862-9</identifier><identifier>PMID: 24100473</identifier><language>eng</language><publisher>Vienna: Springer-Verlag</publisher><subject>Biomedical and Life Sciences ; Biomedicine ; Cell Line, Tumor ; genes ; genotype ; Hepacivirus - physiology ; Hepatitis C ; Hepatitis C virus ; Hepatocytes - virology ; hepatoma ; Host-Pathogen Interactions ; Humans ; Infections ; Infectious Diseases ; interferons ; Liver cancer ; Liver cirrhosis ; Medical Microbiology ; microRNA ; MicroRNAs ; Original Article ; patients ; polymerase chain reaction ; single nucleotide polymorphism ; therapeutics ; Viral infections ; Virology ; Virus Cultivation ; Virus Replication ; Viruses</subject><ispartof>Archives of virology, 2014-03, Vol.159 (3), p.527-534</ispartof><rights>Springer-Verlag Wien 2013</rights><rights>Springer-Verlag Wien 2014</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c495t-187c179d812ba735bdb32b49594c49f6f43f593800a6572dbc924070118a685e3</citedby><cites>FETCH-LOGICAL-c495t-187c179d812ba735bdb32b49594c49f6f43f593800a6572dbc924070118a685e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00705-013-1862-9$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00705-013-1862-9$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24100473$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hoffmann, Thomas Walter</creatorcontrib><creatorcontrib>Delfosse, Fabien</creatorcontrib><creatorcontrib>Helle, François</creatorcontrib><creatorcontrib>François, Catherine</creatorcontrib><creatorcontrib>Duverlie, Gilles</creatorcontrib><creatorcontrib>Castelain, Sandrine</creatorcontrib><title>expression of HCV-associated host factors is dependent on the hepatoma cell line used in HCV studies</title><title>Archives of virology</title><addtitle>Arch Virol</addtitle><addtitle>Arch Virol</addtitle><description>Chronic infection by hepatitis C virus (HCV) is a major cause of liver cirrhosis and hepatocellular carcinoma. At present, the most commonly used in vitro model of HCV infection is based on hepatoma cell lines. However, they were obtained from different patients and different cancers and/or differ in their characteristics and permissiveness to HCV. HCV infection can be modulated by several host factors, so we compared six different hepatoma cell lines that are used as in vitro models for HCV for some of these host factors: the seven known HCV entry factors, the six best-characterized HCV-associated microRNAs, and the two single-nucleotide polymorphisms near the IL28B gene associated with response to pegylated alpha interferon and ribavirin combination therapy, all assessed by quantitative PCR. We showed that the cell lines, including Huh-7 and Huh-7-derived cells, have different microRNA and HCV entry factor expression profiles as well as different IL28B genotypes. In conclusion, some of the observed differences might explain the differences in permissiveness of the cell lines, but, above all, they raise questions about the reliability of in vitro HCV research data gathered to date.</description><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Cell Line, Tumor</subject><subject>genes</subject><subject>genotype</subject><subject>Hepacivirus - physiology</subject><subject>Hepatitis C</subject><subject>Hepatitis C virus</subject><subject>Hepatocytes - virology</subject><subject>hepatoma</subject><subject>Host-Pathogen Interactions</subject><subject>Humans</subject><subject>Infections</subject><subject>Infectious Diseases</subject><subject>interferons</subject><subject>Liver cancer</subject><subject>Liver cirrhosis</subject><subject>Medical Microbiology</subject><subject>microRNA</subject><subject>MicroRNAs</subject><subject>Original Article</subject><subject>patients</subject><subject>polymerase chain reaction</subject><subject>single nucleotide polymorphism</subject><subject>therapeutics</subject><subject>Viral infections</subject><subject>Virology</subject><subject>Virus Cultivation</subject><subject>Virus Replication</subject><subject>Viruses</subject><issn>0304-8608</issn><issn>1432-8798</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNqNkU9v1DAQxS0EokvLB-gFLPXCJeC_iXNEq0KRKnGA9mo58aTrajdOPY5Uvj2OsqCKQ8XFljy_98Yzj5Bzzj5yxppPWA6mK8ZlxU0tqvYF2XAlRWWa1rwkGyaZqkzNzAl5g3jPWHmQ-jU5EaroVSM3xMPjlAAxxJHGgV5tbyuHGPvgMni6i5jp4PocE9KA1MMEo4cx04LnHdAdTC7Hg6M97Pd0H0agMxZhGBcrinn2AfCMvBrcHuHt8T4lN18uf26vquvvX79tP19XvWp1LjM0PW9ab7joXCN15zspulJqVQGGelBy0K00jLlaN8J3fStU2QDnxtVGgzwlH1bfKcWHGTDbQ8DlZ26EOKPlWiojjBDiP9CyKXVEL_5B7-OcxjLIQgmhlG7aQvGV6lNETDDYKYWDS78sZ3ZJy65p2ZKWXdKyi-bd0XnuDuD_Kv7EUwCxAlhK4x2kJ62fcX2_igYXrbtLAe3ND8G4KvmXBfBa_gbYKqW_</recordid><startdate>20140301</startdate><enddate>20140301</enddate><creator>Hoffmann, Thomas Walter</creator><creator>Delfosse, Fabien</creator><creator>Helle, François</creator><creator>François, Catherine</creator><creator>Duverlie, Gilles</creator><creator>Castelain, Sandrine</creator><general>Springer-Verlag</general><general>Springer Vienna</general><general>Springer Nature B.V</general><scope>FBQ</scope><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>3V.</scope><scope>7TK</scope><scope>7TM</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>20140301</creationdate><title>expression of HCV-associated host factors is dependent on the hepatoma cell line used in HCV studies</title><author>Hoffmann, Thomas Walter ; Delfosse, Fabien ; Helle, François ; François, Catherine ; Duverlie, Gilles ; Castelain, Sandrine</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c495t-187c179d812ba735bdb32b49594c49f6f43f593800a6572dbc924070118a685e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Cell Line, Tumor</topic><topic>genes</topic><topic>genotype</topic><topic>Hepacivirus - physiology</topic><topic>Hepatitis C</topic><topic>Hepatitis C virus</topic><topic>Hepatocytes - virology</topic><topic>hepatoma</topic><topic>Host-Pathogen Interactions</topic><topic>Humans</topic><topic>Infections</topic><topic>Infectious Diseases</topic><topic>interferons</topic><topic>Liver cancer</topic><topic>Liver cirrhosis</topic><topic>Medical Microbiology</topic><topic>microRNA</topic><topic>MicroRNAs</topic><topic>Original Article</topic><topic>patients</topic><topic>polymerase chain reaction</topic><topic>single nucleotide polymorphism</topic><topic>therapeutics</topic><topic>Viral infections</topic><topic>Virology</topic><topic>Virus Cultivation</topic><topic>Virus Replication</topic><topic>Viruses</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hoffmann, Thomas Walter</creatorcontrib><creatorcontrib>Delfosse, Fabien</creatorcontrib><creatorcontrib>Helle, François</creatorcontrib><creatorcontrib>François, Catherine</creatorcontrib><creatorcontrib>Duverlie, Gilles</creatorcontrib><creatorcontrib>Castelain, Sandrine</creatorcontrib><collection>AGRIS</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Biological Science Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Archives of virology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hoffmann, Thomas Walter</au><au>Delfosse, Fabien</au><au>Helle, François</au><au>François, Catherine</au><au>Duverlie, Gilles</au><au>Castelain, Sandrine</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>expression of HCV-associated host factors is dependent on the hepatoma cell line used in HCV studies</atitle><jtitle>Archives of virology</jtitle><stitle>Arch Virol</stitle><addtitle>Arch Virol</addtitle><date>2014-03-01</date><risdate>2014</risdate><volume>159</volume><issue>3</issue><spage>527</spage><epage>534</epage><pages>527-534</pages><issn>0304-8608</issn><eissn>1432-8798</eissn><abstract>Chronic infection by hepatitis C virus (HCV) is a major cause of liver cirrhosis and hepatocellular carcinoma. At present, the most commonly used in vitro model of HCV infection is based on hepatoma cell lines. However, they were obtained from different patients and different cancers and/or differ in their characteristics and permissiveness to HCV. HCV infection can be modulated by several host factors, so we compared six different hepatoma cell lines that are used as in vitro models for HCV for some of these host factors: the seven known HCV entry factors, the six best-characterized HCV-associated microRNAs, and the two single-nucleotide polymorphisms near the IL28B gene associated with response to pegylated alpha interferon and ribavirin combination therapy, all assessed by quantitative PCR. We showed that the cell lines, including Huh-7 and Huh-7-derived cells, have different microRNA and HCV entry factor expression profiles as well as different IL28B genotypes. In conclusion, some of the observed differences might explain the differences in permissiveness of the cell lines, but, above all, they raise questions about the reliability of in vitro HCV research data gathered to date.</abstract><cop>Vienna</cop><pub>Springer-Verlag</pub><pmid>24100473</pmid><doi>10.1007/s00705-013-1862-9</doi><tpages>8</tpages></addata></record> |
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subjects | Biomedical and Life Sciences Biomedicine Cell Line, Tumor genes genotype Hepacivirus - physiology Hepatitis C Hepatitis C virus Hepatocytes - virology hepatoma Host-Pathogen Interactions Humans Infections Infectious Diseases interferons Liver cancer Liver cirrhosis Medical Microbiology microRNA MicroRNAs Original Article patients polymerase chain reaction single nucleotide polymorphism therapeutics Viral infections Virology Virus Cultivation Virus Replication Viruses |
title | expression of HCV-associated host factors is dependent on the hepatoma cell line used in HCV studies |
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