Down-regulation of RUNX1, RUNX3 and CBFbeta in hepatocellular carcinomas in an early stage of hepatocarcinogenesis
Our previous studies suggested that deficient function of RUNX3 protein is causally related to development and progression of human gastric cancer. RUNX3 is mapped to 1p36, which is frequently deleted in hepatocellular carcinomas (HCC), therefore, these tumors were investigated for expression and co...
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Veröffentlicht in: | Anticancer research 2006-09, Vol.26 (5B), p.3633-3643 |
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creator | Miyagawa, Kouji Sakakura, Chouhei Nakashima, Susumu Yoshikawa, Tetsuji Kin, Shuichi Nakase, Yuenn Ito, Kosei Yamagishi, Hisakazu Ida, Hiroshi Yazumi, Shujiro Chiba, Tsutomu Ito, Yoshiaki Hagiwara, Akeo |
description | Our previous studies suggested that deficient function of RUNX3 protein is causally related to development and progression of human gastric cancer. RUNX3 is mapped to 1p36, which is frequently deleted in hepatocellular carcinomas (HCC), therefore, these tumors were investigated for expression and copy number changes of RUNX3 and other Runt-related genes, RUNX1, RUNX2, and their co-factor CBFP. Similarly nearby uninvolved liver showing cirrhosis or normal histology was investigated in conjunction with various clinicopathological factors.
Copy number change and expression change of RUNX family genes in 35 hepatocellular carcinoma specimens and adjoining liver with cirrhosis (LC) or normal histology were estimated using quantitative reverse transcription polymerase chain reaction (RT-PCR) and in situ hybridization. |
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Copy number change and expression change of RUNX family genes in 35 hepatocellular carcinoma specimens and adjoining liver with cirrhosis (LC) or normal histology were estimated using quantitative reverse transcription polymerase chain reaction (RT-PCR) and in situ hybridization.</description><identifier>ISSN: 0250-7005</identifier><identifier>PMID: 17094378</identifier><language>eng</language><publisher>Greece</publisher><subject>Base Sequence ; Carcinoma, Hepatocellular - genetics ; Core Binding Factor Alpha 2 Subunit - genetics ; Core Binding Factor Alpha 3 Subunit - genetics ; Core Binding Factor alpha Subunits - genetics ; DNA Primers ; Down-Regulation ; Gene Deletion ; Humans ; In Situ Hybridization, Fluorescence ; Liver - metabolism ; Liver Cirrhosis - genetics ; Liver Neoplasms - genetics ; Molecular Sequence Data ; Reverse Transcriptase Polymerase Chain Reaction ; Sequence Homology, Nucleic Acid</subject><ispartof>Anticancer research, 2006-09, Vol.26 (5B), p.3633-3643</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17094378$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Miyagawa, Kouji</creatorcontrib><creatorcontrib>Sakakura, Chouhei</creatorcontrib><creatorcontrib>Nakashima, Susumu</creatorcontrib><creatorcontrib>Yoshikawa, Tetsuji</creatorcontrib><creatorcontrib>Kin, Shuichi</creatorcontrib><creatorcontrib>Nakase, Yuenn</creatorcontrib><creatorcontrib>Ito, Kosei</creatorcontrib><creatorcontrib>Yamagishi, Hisakazu</creatorcontrib><creatorcontrib>Ida, Hiroshi</creatorcontrib><creatorcontrib>Yazumi, Shujiro</creatorcontrib><creatorcontrib>Chiba, Tsutomu</creatorcontrib><creatorcontrib>Ito, Yoshiaki</creatorcontrib><creatorcontrib>Hagiwara, Akeo</creatorcontrib><title>Down-regulation of RUNX1, RUNX3 and CBFbeta in hepatocellular carcinomas in an early stage of hepatocarcinogenesis</title><title>Anticancer research</title><addtitle>Anticancer Res</addtitle><description>Our previous studies suggested that deficient function of RUNX3 protein is causally related to development and progression of human gastric cancer. RUNX3 is mapped to 1p36, which is frequently deleted in hepatocellular carcinomas (HCC), therefore, these tumors were investigated for expression and copy number changes of RUNX3 and other Runt-related genes, RUNX1, RUNX2, and their co-factor CBFP. Similarly nearby uninvolved liver showing cirrhosis or normal histology was investigated in conjunction with various clinicopathological factors.
Copy number change and expression change of RUNX family genes in 35 hepatocellular carcinoma specimens and adjoining liver with cirrhosis (LC) or normal histology were estimated using quantitative reverse transcription polymerase chain reaction (RT-PCR) and in situ hybridization.</description><subject>Base Sequence</subject><subject>Carcinoma, Hepatocellular - genetics</subject><subject>Core Binding Factor Alpha 2 Subunit - genetics</subject><subject>Core Binding Factor Alpha 3 Subunit - genetics</subject><subject>Core Binding Factor alpha Subunits - genetics</subject><subject>DNA Primers</subject><subject>Down-Regulation</subject><subject>Gene Deletion</subject><subject>Humans</subject><subject>In Situ Hybridization, Fluorescence</subject><subject>Liver - metabolism</subject><subject>Liver Cirrhosis - genetics</subject><subject>Liver Neoplasms - genetics</subject><subject>Molecular Sequence Data</subject><subject>Reverse Transcriptase Polymerase Chain Reaction</subject><subject>Sequence Homology, Nucleic Acid</subject><issn>0250-7005</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo1kDFPwzAUhD2AaCn8BeSJiUhOXDv2CIUCUgUSKhJb9Oy8lKDEDnYi1H9PQ8N0w313Ot0JmbNMsCRnTMzIeYxfjEmpFT8jszRneslzNSfh3v-4JOBuaKCvvaO-om_vLx_pzZ9wCq6kq7u1wR5o7egndtB7i01zCARqIdja-RbiaIKjCKHZ09jDDseqCT9SO3QY63hBTitoIl5OuiDb9cN29ZRsXh-fV7ebpBNLlYBJrZFMVBqt4UJpLCU3vNSGccOMFZqliuc6K22VSSbzTFmlqspKmYHOBF-Q62NtF_z3gLEv2jqOw8GhH2IhVcoPL4zg1QQOpsWy6ELdQtgX_yfxX3-nYnM</recordid><startdate>200609</startdate><enddate>200609</enddate><creator>Miyagawa, Kouji</creator><creator>Sakakura, Chouhei</creator><creator>Nakashima, Susumu</creator><creator>Yoshikawa, Tetsuji</creator><creator>Kin, Shuichi</creator><creator>Nakase, Yuenn</creator><creator>Ito, Kosei</creator><creator>Yamagishi, Hisakazu</creator><creator>Ida, Hiroshi</creator><creator>Yazumi, Shujiro</creator><creator>Chiba, Tsutomu</creator><creator>Ito, Yoshiaki</creator><creator>Hagiwara, Akeo</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>200609</creationdate><title>Down-regulation of RUNX1, RUNX3 and CBFbeta in hepatocellular carcinomas in an early stage of hepatocarcinogenesis</title><author>Miyagawa, Kouji ; Sakakura, Chouhei ; Nakashima, Susumu ; Yoshikawa, Tetsuji ; Kin, Shuichi ; Nakase, Yuenn ; Ito, Kosei ; Yamagishi, Hisakazu ; Ida, Hiroshi ; Yazumi, Shujiro ; Chiba, Tsutomu ; Ito, Yoshiaki ; Hagiwara, Akeo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p548-ab1cb605f9ecb3589ed63b3d9b03b0bc590183792dcf2606728c88ffc662a9253</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Base Sequence</topic><topic>Carcinoma, Hepatocellular - genetics</topic><topic>Core Binding Factor Alpha 2 Subunit - genetics</topic><topic>Core Binding Factor Alpha 3 Subunit - genetics</topic><topic>Core Binding Factor alpha Subunits - genetics</topic><topic>DNA Primers</topic><topic>Down-Regulation</topic><topic>Gene Deletion</topic><topic>Humans</topic><topic>In Situ Hybridization, Fluorescence</topic><topic>Liver - metabolism</topic><topic>Liver Cirrhosis - genetics</topic><topic>Liver Neoplasms - genetics</topic><topic>Molecular Sequence Data</topic><topic>Reverse Transcriptase Polymerase Chain Reaction</topic><topic>Sequence Homology, Nucleic Acid</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Miyagawa, Kouji</creatorcontrib><creatorcontrib>Sakakura, Chouhei</creatorcontrib><creatorcontrib>Nakashima, Susumu</creatorcontrib><creatorcontrib>Yoshikawa, Tetsuji</creatorcontrib><creatorcontrib>Kin, Shuichi</creatorcontrib><creatorcontrib>Nakase, Yuenn</creatorcontrib><creatorcontrib>Ito, Kosei</creatorcontrib><creatorcontrib>Yamagishi, Hisakazu</creatorcontrib><creatorcontrib>Ida, Hiroshi</creatorcontrib><creatorcontrib>Yazumi, Shujiro</creatorcontrib><creatorcontrib>Chiba, Tsutomu</creatorcontrib><creatorcontrib>Ito, Yoshiaki</creatorcontrib><creatorcontrib>Hagiwara, Akeo</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>Anticancer research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Miyagawa, Kouji</au><au>Sakakura, Chouhei</au><au>Nakashima, Susumu</au><au>Yoshikawa, Tetsuji</au><au>Kin, Shuichi</au><au>Nakase, Yuenn</au><au>Ito, Kosei</au><au>Yamagishi, Hisakazu</au><au>Ida, Hiroshi</au><au>Yazumi, Shujiro</au><au>Chiba, Tsutomu</au><au>Ito, Yoshiaki</au><au>Hagiwara, Akeo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Down-regulation of RUNX1, RUNX3 and CBFbeta in hepatocellular carcinomas in an early stage of hepatocarcinogenesis</atitle><jtitle>Anticancer research</jtitle><addtitle>Anticancer Res</addtitle><date>2006-09</date><risdate>2006</risdate><volume>26</volume><issue>5B</issue><spage>3633</spage><epage>3643</epage><pages>3633-3643</pages><issn>0250-7005</issn><abstract>Our previous studies suggested that deficient function of RUNX3 protein is causally related to development and progression of human gastric cancer. RUNX3 is mapped to 1p36, which is frequently deleted in hepatocellular carcinomas (HCC), therefore, these tumors were investigated for expression and copy number changes of RUNX3 and other Runt-related genes, RUNX1, RUNX2, and their co-factor CBFP. Similarly nearby uninvolved liver showing cirrhosis or normal histology was investigated in conjunction with various clinicopathological factors.
Copy number change and expression change of RUNX family genes in 35 hepatocellular carcinoma specimens and adjoining liver with cirrhosis (LC) or normal histology were estimated using quantitative reverse transcription polymerase chain reaction (RT-PCR) and in situ hybridization.</abstract><cop>Greece</cop><pmid>17094378</pmid><tpages>11</tpages></addata></record> |
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subjects | Base Sequence Carcinoma, Hepatocellular - genetics Core Binding Factor Alpha 2 Subunit - genetics Core Binding Factor Alpha 3 Subunit - genetics Core Binding Factor alpha Subunits - genetics DNA Primers Down-Regulation Gene Deletion Humans In Situ Hybridization, Fluorescence Liver - metabolism Liver Cirrhosis - genetics Liver Neoplasms - genetics Molecular Sequence Data Reverse Transcriptase Polymerase Chain Reaction Sequence Homology, Nucleic Acid |
title | Down-regulation of RUNX1, RUNX3 and CBFbeta in hepatocellular carcinomas in an early stage of hepatocarcinogenesis |
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