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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
Main Authors: Marchio, A, Terris, B, Meddeb, M, Pineau, P, Duverger, A, Tiollais, P, Bernheim, A, Dejean, A
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container_issue 4
container_start_page 270
container_title Molecular pathology
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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. 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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. 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ispartof Molecular pathology, 2001-08, Vol.54 (4), p.270-274
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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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