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Chromosomal abnormalities in liver cell dysplasia detected by comparative genomic hybridisation
Background/Aim—The pathogenetic relation between liver cell dysplasia and hepatocellular carcinoma (HCC) is poorly understood. The aim of this study was to determine whether there is a genetic link between liver cell dysplasia and HCC that could support the role of dysplasia as a tumour precursor le...
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Published in: | Molecular pathology 2001-08, Vol.54 (4), p.270-274 |
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creator | Marchio, A Terris, B Meddeb, M Pineau, P Duverger, A Tiollais, P Bernheim, A Dejean, A |
description | Background/Aim—The pathogenetic relation between liver cell dysplasia and hepatocellular carcinoma (HCC) is poorly understood. The aim of this study was to determine whether there is a genetic link between liver cell dysplasia and HCC that could support the role of dysplasia as a tumour precursor lesion. Methods—Microdissection from paraffin wax embedded sections and degenerate oligonucleotide primed polymerase chain reaction (DOP-PCR) were combined to analyse chromosomal imbalances by comparative genomic hybridisation (CGH) in nine HCCs and nodules containing liver cell dysplasia and cirrhosis adjacent to the tumours. Seven cases of large cell changes (LCC) and three cases of small cell changes (SCC) were analysed. The genetic abnormalities detected in liver cell dysplasia were then compared with those present in the corresponding HCC. Results—No abnormalities were detected in LCC and cirrhotic nodules, arguing against the preneoplasic nature of these cell foci. In contrast, a subset of chromosomal alterations present in HCCs was found in the adjacent SCC. Conclusions—These findings support the preneoplastic status of SCC in human hepatocarcinogenesis. |
doi_str_mv | 10.1136/mp.54.4.270 |
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The aim of this study was to determine whether there is a genetic link between liver cell dysplasia and HCC that could support the role of dysplasia as a tumour precursor lesion. Methods—Microdissection from paraffin wax embedded sections and degenerate oligonucleotide primed polymerase chain reaction (DOP-PCR) were combined to analyse chromosomal imbalances by comparative genomic hybridisation (CGH) in nine HCCs and nodules containing liver cell dysplasia and cirrhosis adjacent to the tumours. Seven cases of large cell changes (LCC) and three cases of small cell changes (SCC) were analysed. The genetic abnormalities detected in liver cell dysplasia were then compared with those present in the corresponding HCC. Results—No abnormalities were detected in LCC and cirrhotic nodules, arguing against the preneoplasic nature of these cell foci. In contrast, a subset of chromosomal alterations present in HCCs was found in the adjacent SCC. Conclusions—These findings support the preneoplastic status of SCC in human hepatocarcinogenesis.</description><identifier>ISSN: 1366-8714</identifier><identifier>EISSN: 1472-4154</identifier><identifier>DOI: 10.1136/mp.54.4.270</identifier><identifier>PMID: 11477144</identifier><language>eng</language><publisher>London: BMJ Publishing Group Ltd and Association of Clinical Pathologists</publisher><subject>Abnormalities ; Biochemistry, Molecular Biology ; Biological and medical sciences ; Cancer ; Carcinoma, Hepatocellular - genetics ; Carcinoma, Hepatocellular - pathology ; Chromosome Aberrations - diagnosis ; Chromosome Disorders ; comparative genomic hybridisation ; Development and progression ; Gastroenterology. Liver. Pancreas. Abdomen ; Genomics ; hepatocellular carcinoma ; Hepatocytes - pathology ; Human health and pathology ; Humans ; Hépatology and Gastroenterology ; Image Processing, Computer-Assisted ; Life Sciences ; Liver cancer ; liver cell dysplasia ; Liver cells ; Liver Cirrhosis - genetics ; Liver Neoplasms - genetics ; Liver Neoplasms - pathology ; Liver. Biliary tract. Portal circulation. Exocrine pancreas ; Medical sciences ; Microscopy, Fluorescence ; Molecular biology ; Nucleic Acid Hybridization ; Polymerase Chain Reaction - methods ; Precancerous Conditions - genetics ; Tumors</subject><ispartof>Molecular pathology, 2001-08, Vol.54 (4), p.270-274</ispartof><rights>COPYRIGHT © 2001 Journal of Clinical Pathology</rights><rights>2001 INIST-CNRS</rights><rights>COPYRIGHT 2001 BMJ Publishing Group Ltd.</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><rights>Copyright © 2001, Journal of Clinical Pathology 2001</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b588t-d51076fade4a61356621de80d55aefa7713cea9e18f7839046a2bb1d830761543</citedby><orcidid>0000-0001-6541-5395 ; 0000-0002-9407-1592 ; 0000-0003-4778-6840</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1187080/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1187080/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,27922,27923,53789,53791</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=1131019$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11477144$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://pasteur.hal.science/pasteur-02872364$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Marchio, A</creatorcontrib><creatorcontrib>Terris, B</creatorcontrib><creatorcontrib>Meddeb, M</creatorcontrib><creatorcontrib>Pineau, P</creatorcontrib><creatorcontrib>Duverger, A</creatorcontrib><creatorcontrib>Tiollais, P</creatorcontrib><creatorcontrib>Bernheim, A</creatorcontrib><creatorcontrib>Dejean, A</creatorcontrib><title>Chromosomal abnormalities in liver cell dysplasia detected by comparative genomic hybridisation</title><title>Molecular pathology</title><addtitle>Mol Path</addtitle><description>Background/Aim—The pathogenetic relation between liver cell dysplasia and hepatocellular carcinoma (HCC) is poorly understood. The aim of this study was to determine whether there is a genetic link between liver cell dysplasia and HCC that could support the role of dysplasia as a tumour precursor lesion. Methods—Microdissection from paraffin wax embedded sections and degenerate oligonucleotide primed polymerase chain reaction (DOP-PCR) were combined to analyse chromosomal imbalances by comparative genomic hybridisation (CGH) in nine HCCs and nodules containing liver cell dysplasia and cirrhosis adjacent to the tumours. Seven cases of large cell changes (LCC) and three cases of small cell changes (SCC) were analysed. The genetic abnormalities detected in liver cell dysplasia were then compared with those present in the corresponding HCC. Results—No abnormalities were detected in LCC and cirrhotic nodules, arguing against the preneoplasic nature of these cell foci. In contrast, a subset of chromosomal alterations present in HCCs was found in the adjacent SCC. Conclusions—These findings support the preneoplastic status of SCC in human hepatocarcinogenesis.</description><subject>Abnormalities</subject><subject>Biochemistry, Molecular Biology</subject><subject>Biological and medical sciences</subject><subject>Cancer</subject><subject>Carcinoma, Hepatocellular - genetics</subject><subject>Carcinoma, Hepatocellular - pathology</subject><subject>Chromosome Aberrations - diagnosis</subject><subject>Chromosome Disorders</subject><subject>comparative genomic hybridisation</subject><subject>Development and progression</subject><subject>Gastroenterology. Liver. Pancreas. Abdomen</subject><subject>Genomics</subject><subject>hepatocellular carcinoma</subject><subject>Hepatocytes - pathology</subject><subject>Human health and pathology</subject><subject>Humans</subject><subject>Hépatology and Gastroenterology</subject><subject>Image Processing, Computer-Assisted</subject><subject>Life Sciences</subject><subject>Liver cancer</subject><subject>liver cell dysplasia</subject><subject>Liver cells</subject><subject>Liver Cirrhosis - genetics</subject><subject>Liver Neoplasms - genetics</subject><subject>Liver Neoplasms - pathology</subject><subject>Liver. Biliary tract. Portal circulation. Exocrine pancreas</subject><subject>Medical sciences</subject><subject>Microscopy, Fluorescence</subject><subject>Molecular biology</subject><subject>Nucleic Acid Hybridization</subject><subject>Polymerase Chain Reaction - methods</subject><subject>Precancerous Conditions - genetics</subject><subject>Tumors</subject><issn>1366-8714</issn><issn>1472-4154</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><recordid>eNp9kkGP0zAQhSMEYpeFE3eUA-ICKXbi2O4FqSosRVTLBVZ7sybxpPWSxMFOK_rvmVWrbRch5INHM59nnp-dJC85m3BeyPfdMCnFRExyxR4l51yoPBO8FI8pLqTMtOLiLHkW4y1jTItcP03OOFGUFueJma-D73z0HbQpVL0PFLjRYUxdn7ZuiyGtsW1Tu4tDC9FBanHEekSbVru09t0AAUbi0hX2vnN1ut5VwVkXKev758mTBtqILw77RfLj8tP3-SJbfvv8ZT5bZlWp9ZjZkjMlG7AoQPKilDLnFjWzZQnYAIktaoQpct0oXUyZkJBXFbe6oGN02eIi-bDvO2yqDm2N_RigNUNwHYSd8eDMw0rv1mblt4ZzrZhm1CDbN1j_dWwxW5oB4oibYFiuVV5IseXEvzkMDP7XBuNoOhfvnIIe_SYaxVnJpZ4S-G4PrqBF4_rG0_yazEKS4XtsHKVnSml6v_xExwOclkUy91_82z1fBx9jwOZePGfm7n-YbjClMMIQT_SrU5uO7OFDEPD6AECsoW0C9LWLJ1zBGZ8eVToy5vd9GcJPI1WhSnN1PTeXVx_V4uvNjbk-ulV1t_8V-AcwX9-V</recordid><startdate>20010801</startdate><enddate>20010801</enddate><creator>Marchio, A</creator><creator>Terris, B</creator><creator>Meddeb, M</creator><creator>Pineau, P</creator><creator>Duverger, A</creator><creator>Tiollais, P</creator><creator>Bernheim, A</creator><creator>Dejean, A</creator><general>BMJ Publishing Group Ltd and Association of Clinical Pathologists</general><general>BMJ</general><general>BMJ Publishing Group Ltd</general><general>BMJ Publishing Group</general><general>British Medical Journal Publishing Group</general><scope>BSCLL</scope><scope>IQODW</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>7X8</scope><scope>1XC</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-6541-5395</orcidid><orcidid>https://orcid.org/0000-0002-9407-1592</orcidid><orcidid>https://orcid.org/0000-0003-4778-6840</orcidid></search><sort><creationdate>20010801</creationdate><title>Chromosomal abnormalities in liver cell dysplasia detected by comparative genomic hybridisation</title><author>Marchio, A ; Terris, B ; Meddeb, M ; Pineau, P ; Duverger, A ; Tiollais, P ; Bernheim, A ; Dejean, A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b588t-d51076fade4a61356621de80d55aefa7713cea9e18f7839046a2bb1d830761543</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>Abnormalities</topic><topic>Biochemistry, Molecular Biology</topic><topic>Biological and medical sciences</topic><topic>Cancer</topic><topic>Carcinoma, Hepatocellular - genetics</topic><topic>Carcinoma, Hepatocellular - pathology</topic><topic>Chromosome Aberrations - diagnosis</topic><topic>Chromosome Disorders</topic><topic>comparative genomic hybridisation</topic><topic>Development and progression</topic><topic>Gastroenterology. Liver. Pancreas. Abdomen</topic><topic>Genomics</topic><topic>hepatocellular carcinoma</topic><topic>Hepatocytes - pathology</topic><topic>Human health and pathology</topic><topic>Humans</topic><topic>Hépatology and Gastroenterology</topic><topic>Image Processing, Computer-Assisted</topic><topic>Life Sciences</topic><topic>Liver cancer</topic><topic>liver cell dysplasia</topic><topic>Liver cells</topic><topic>Liver Cirrhosis - genetics</topic><topic>Liver Neoplasms - genetics</topic><topic>Liver Neoplasms - pathology</topic><topic>Liver. Biliary tract. Portal circulation. Exocrine pancreas</topic><topic>Medical sciences</topic><topic>Microscopy, Fluorescence</topic><topic>Molecular biology</topic><topic>Nucleic Acid Hybridization</topic><topic>Polymerase Chain Reaction - methods</topic><topic>Precancerous Conditions - genetics</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Marchio, A</creatorcontrib><creatorcontrib>Terris, B</creatorcontrib><creatorcontrib>Meddeb, M</creatorcontrib><creatorcontrib>Pineau, P</creatorcontrib><creatorcontrib>Duverger, A</creatorcontrib><creatorcontrib>Tiollais, P</creatorcontrib><creatorcontrib>Bernheim, A</creatorcontrib><creatorcontrib>Dejean, A</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><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>Hyper Article en Ligne (HAL)</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Molecular pathology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Marchio, A</au><au>Terris, B</au><au>Meddeb, M</au><au>Pineau, P</au><au>Duverger, A</au><au>Tiollais, P</au><au>Bernheim, A</au><au>Dejean, A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Chromosomal abnormalities in liver cell dysplasia detected by comparative genomic hybridisation</atitle><jtitle>Molecular pathology</jtitle><addtitle>Mol Path</addtitle><date>2001-08-01</date><risdate>2001</risdate><volume>54</volume><issue>4</issue><spage>270</spage><epage>274</epage><pages>270-274</pages><issn>1366-8714</issn><eissn>1472-4154</eissn><abstract>Background/Aim—The pathogenetic relation between liver cell dysplasia and hepatocellular carcinoma (HCC) is poorly understood. The aim of this study was to determine whether there is a genetic link between liver cell dysplasia and HCC that could support the role of dysplasia as a tumour precursor lesion. Methods—Microdissection from paraffin wax embedded sections and degenerate oligonucleotide primed polymerase chain reaction (DOP-PCR) were combined to analyse chromosomal imbalances by comparative genomic hybridisation (CGH) in nine HCCs and nodules containing liver cell dysplasia and cirrhosis adjacent to the tumours. Seven cases of large cell changes (LCC) and three cases of small cell changes (SCC) were analysed. The genetic abnormalities detected in liver cell dysplasia were then compared with those present in the corresponding HCC. Results—No abnormalities were detected in LCC and cirrhotic nodules, arguing against the preneoplasic nature of these cell foci. In contrast, a subset of chromosomal alterations present in HCCs was found in the adjacent SCC. 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subjects | Abnormalities Biochemistry, Molecular Biology Biological and medical sciences Cancer Carcinoma, Hepatocellular - genetics Carcinoma, Hepatocellular - pathology Chromosome Aberrations - diagnosis Chromosome Disorders comparative genomic hybridisation Development and progression Gastroenterology. Liver. Pancreas. Abdomen Genomics hepatocellular carcinoma Hepatocytes - pathology Human health and pathology Humans Hépatology and Gastroenterology Image Processing, Computer-Assisted Life Sciences Liver cancer liver cell dysplasia Liver cells Liver Cirrhosis - genetics Liver Neoplasms - genetics Liver Neoplasms - pathology Liver. Biliary tract. Portal circulation. Exocrine pancreas Medical sciences Microscopy, Fluorescence Molecular biology Nucleic Acid Hybridization Polymerase Chain Reaction - methods Precancerous Conditions - genetics Tumors |
title | Chromosomal abnormalities in liver cell dysplasia detected by comparative genomic hybridisation |
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