A Relation Between Cell Cycle and Intestinal Metaplasia in Oesophageal Biopsies Using Optical and Digital Microscopy

Protein expression changes in relation to cell cycles provide important information, and it may represent a new method for an early diagnosis of metaplasia – dysplasia – adenocarcinoma sequence. We investigated potential changes in cell cycle genes such as protooncogenes (PCNA, EGFR), tumour suppres...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Pathology oncology research 2015-07, Vol.21 (3), p.669-673
Hauptverfasser: Mate, Miklos, Molnar, Bela
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 673
container_issue 3
container_start_page 669
container_title Pathology oncology research
container_volume 21
creator Mate, Miklos
Molnar, Bela
description Protein expression changes in relation to cell cycles provide important information, and it may represent a new method for an early diagnosis of metaplasia – dysplasia – adenocarcinoma sequence. We investigated potential changes in cell cycle genes such as protooncogenes (PCNA, EGFR), tumour suppressor gene (p53), apoptotic TUNNEL (Tdt mediated dUTP nick and labelling) gene, as well as small intestinal mucus antigen (SIMA) and large intestinal mucus antigen (LIMA), which accumulates in metaplastic epithelium due to the inflammatory process in routine oesophageal biopsies using immunohistochemistry. Oesophageal biopsies were taken from patients with Barrett’s oesophagus ( n  = 30), reflux oesophagitis ( n  = 30), healthy oesophagus ( n  = 30) and healthy cardia ( n  = 10). Immunohistochemical signalling was carried out by Streptavidin-Biotin-AEC (aminoetil-carbazol). Expression of PCNA was statistically significantly lower in healthy oesophagus ( p   0.05).
doi_str_mv 10.1007/s12253-014-9873-8
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1819147250</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1819147250</sourcerecordid><originalsourceid>FETCH-LOGICAL-c427t-d9ef50f36fb0476efde3d1ee51f8ac01f38985db4ffa35eeff34cd39b35a66cc3</originalsourceid><addsrcrecordid>eNqFkV1LHDEYhYNUqlV_QG8k0JveTM33JJe6_RIsC0WvQzbzZhuZzYyTLGX_fTNdLVIQr_LxPueEk4PQe0o-UULai0wZk7whVDRGt7zRB-iYSs4apkn7pu4ZNY0wUh2hdznfk6pRRr1FR0y2oh7oMSqX-Cf0rsQh4SsovwESXkDf48XO94Bd6vB1KpBLTK7HP6C4sXc5OhwTXkIexl9uDXVyFYcxR8j4Lse0xsuxRF-vZ_3nuI5lFkc_DdkP4-4UHQbXZzh7XE_Q3dcvt4vvzc3y2_Xi8qbxgrWl6QwESQJXYUVEqyB0wDsKIGnQzhMauDZadisRguMSIAQufMfNikunlPf8BH3c-47T8LCtIewmZl_TuQTDNluqqaGiZZK8jiqtiNLCiIp--A-9H7ZT_Z6_lKRCSC0rRffUHDpPEOw4xY2bdpYSO7dn9-3Z2p6d27O6as4fnberDXT_FE91VYDtgVxHaQ3Ts6dfdP0DFVilfQ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1685144585</pqid></control><display><type>article</type><title>A Relation Between Cell Cycle and Intestinal Metaplasia in Oesophageal Biopsies Using Optical and Digital Microscopy</title><source>MEDLINE</source><source>SpringerLink Journals - AutoHoldings</source><creator>Mate, Miklos ; Molnar, Bela</creator><creatorcontrib>Mate, Miklos ; Molnar, Bela</creatorcontrib><description>Protein expression changes in relation to cell cycles provide important information, and it may represent a new method for an early diagnosis of metaplasia – dysplasia – adenocarcinoma sequence. We investigated potential changes in cell cycle genes such as protooncogenes (PCNA, EGFR), tumour suppressor gene (p53), apoptotic TUNNEL (Tdt mediated dUTP nick and labelling) gene, as well as small intestinal mucus antigen (SIMA) and large intestinal mucus antigen (LIMA), which accumulates in metaplastic epithelium due to the inflammatory process in routine oesophageal biopsies using immunohistochemistry. Oesophageal biopsies were taken from patients with Barrett’s oesophagus ( n  = 30), reflux oesophagitis ( n  = 30), healthy oesophagus ( n  = 30) and healthy cardia ( n  = 10). Immunohistochemical signalling was carried out by Streptavidin-Biotin-AEC (aminoetil-carbazol). Expression of PCNA was statistically significantly lower in healthy oesophagus ( p  &lt; 0.05) versus reflux oesophagitis and Barrett’s oesophagus. However, no significant change was detected in the expression of SIMA and LIMA in intestinal metaplasia. Further, EGFR, p53 and TUNNEL levels were significantly different in healthy versus Barrett’s oesophagus. Manual counting using virtual microscopy was comparable with the result using conventional light microscopy, but the former is significantly quicker. There was no difference between manual and automated cell counting ( p  &gt; 0.05).</description><identifier>ISSN: 1219-4956</identifier><identifier>EISSN: 1532-2807</identifier><identifier>DOI: 10.1007/s12253-014-9873-8</identifier><identifier>PMID: 25740071</identifier><language>eng</language><publisher>Dordrecht: Springer Netherlands</publisher><subject>Barrett Esophagus - metabolism ; Barrett Esophagus - pathology ; Barrett Esophagus - surgery ; Biomarkers - metabolism ; Biomedical and Life Sciences ; Biomedicine ; Biopsy ; Cancer Research ; Cell Cycle ; Esophagus - metabolism ; Esophagus - pathology ; Esophagus - surgery ; Humans ; Image Interpretation, Computer-Assisted ; Immunoenzyme Techniques ; Immunology ; Intestinal Diseases - metabolism ; Intestinal Diseases - pathology ; Intestinal Diseases - surgery ; Metaplasia - metabolism ; Metaplasia - pathology ; Metaplasia - surgery ; Microscopy - instrumentation ; Oncology ; Optical Imaging ; Pathology ; Prognosis</subject><ispartof>Pathology oncology research, 2015-07, Vol.21 (3), p.669-673</ispartof><rights>Arányi Lajos Foundation 2015</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c427t-d9ef50f36fb0476efde3d1ee51f8ac01f38985db4ffa35eeff34cd39b35a66cc3</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/s12253-014-9873-8$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s12253-014-9873-8$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27915,27916,41479,42548,51310</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25740071$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mate, Miklos</creatorcontrib><creatorcontrib>Molnar, Bela</creatorcontrib><title>A Relation Between Cell Cycle and Intestinal Metaplasia in Oesophageal Biopsies Using Optical and Digital Microscopy</title><title>Pathology oncology research</title><addtitle>Pathol. Oncol. Res</addtitle><addtitle>Pathol Oncol Res</addtitle><description>Protein expression changes in relation to cell cycles provide important information, and it may represent a new method for an early diagnosis of metaplasia – dysplasia – adenocarcinoma sequence. We investigated potential changes in cell cycle genes such as protooncogenes (PCNA, EGFR), tumour suppressor gene (p53), apoptotic TUNNEL (Tdt mediated dUTP nick and labelling) gene, as well as small intestinal mucus antigen (SIMA) and large intestinal mucus antigen (LIMA), which accumulates in metaplastic epithelium due to the inflammatory process in routine oesophageal biopsies using immunohistochemistry. Oesophageal biopsies were taken from patients with Barrett’s oesophagus ( n  = 30), reflux oesophagitis ( n  = 30), healthy oesophagus ( n  = 30) and healthy cardia ( n  = 10). Immunohistochemical signalling was carried out by Streptavidin-Biotin-AEC (aminoetil-carbazol). Expression of PCNA was statistically significantly lower in healthy oesophagus ( p  &lt; 0.05) versus reflux oesophagitis and Barrett’s oesophagus. However, no significant change was detected in the expression of SIMA and LIMA in intestinal metaplasia. Further, EGFR, p53 and TUNNEL levels were significantly different in healthy versus Barrett’s oesophagus. Manual counting using virtual microscopy was comparable with the result using conventional light microscopy, but the former is significantly quicker. There was no difference between manual and automated cell counting ( p  &gt; 0.05).</description><subject>Barrett Esophagus - metabolism</subject><subject>Barrett Esophagus - pathology</subject><subject>Barrett Esophagus - surgery</subject><subject>Biomarkers - metabolism</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Biopsy</subject><subject>Cancer Research</subject><subject>Cell Cycle</subject><subject>Esophagus - metabolism</subject><subject>Esophagus - pathology</subject><subject>Esophagus - surgery</subject><subject>Humans</subject><subject>Image Interpretation, Computer-Assisted</subject><subject>Immunoenzyme Techniques</subject><subject>Immunology</subject><subject>Intestinal Diseases - metabolism</subject><subject>Intestinal Diseases - pathology</subject><subject>Intestinal Diseases - surgery</subject><subject>Metaplasia - metabolism</subject><subject>Metaplasia - pathology</subject><subject>Metaplasia - surgery</subject><subject>Microscopy - instrumentation</subject><subject>Oncology</subject><subject>Optical Imaging</subject><subject>Pathology</subject><subject>Prognosis</subject><issn>1219-4956</issn><issn>1532-2807</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNqFkV1LHDEYhYNUqlV_QG8k0JveTM33JJe6_RIsC0WvQzbzZhuZzYyTLGX_fTNdLVIQr_LxPueEk4PQe0o-UULai0wZk7whVDRGt7zRB-iYSs4apkn7pu4ZNY0wUh2hdznfk6pRRr1FR0y2oh7oMSqX-Cf0rsQh4SsovwESXkDf48XO94Bd6vB1KpBLTK7HP6C4sXc5OhwTXkIexl9uDXVyFYcxR8j4Lse0xsuxRF-vZ_3nuI5lFkc_DdkP4-4UHQbXZzh7XE_Q3dcvt4vvzc3y2_Xi8qbxgrWl6QwESQJXYUVEqyB0wDsKIGnQzhMauDZadisRguMSIAQufMfNikunlPf8BH3c-47T8LCtIewmZl_TuQTDNluqqaGiZZK8jiqtiNLCiIp--A-9H7ZT_Z6_lKRCSC0rRffUHDpPEOw4xY2bdpYSO7dn9-3Z2p6d27O6as4fnberDXT_FE91VYDtgVxHaQ3Ts6dfdP0DFVilfQ</recordid><startdate>20150701</startdate><enddate>20150701</enddate><creator>Mate, Miklos</creator><creator>Molnar, Bela</creator><general>Springer Netherlands</general><general>Springer Nature B.V</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>3V.</scope><scope>7RV</scope><scope>7T5</scope><scope>7TM</scope><scope>7TO</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>H94</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>7X8</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope></search><sort><creationdate>20150701</creationdate><title>A Relation Between Cell Cycle and Intestinal Metaplasia in Oesophageal Biopsies Using Optical and Digital Microscopy</title><author>Mate, Miklos ; Molnar, Bela</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c427t-d9ef50f36fb0476efde3d1ee51f8ac01f38985db4ffa35eeff34cd39b35a66cc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Barrett Esophagus - metabolism</topic><topic>Barrett Esophagus - pathology</topic><topic>Barrett Esophagus - surgery</topic><topic>Biomarkers - metabolism</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Biopsy</topic><topic>Cancer Research</topic><topic>Cell Cycle</topic><topic>Esophagus - metabolism</topic><topic>Esophagus - pathology</topic><topic>Esophagus - surgery</topic><topic>Humans</topic><topic>Image Interpretation, Computer-Assisted</topic><topic>Immunoenzyme Techniques</topic><topic>Immunology</topic><topic>Intestinal Diseases - metabolism</topic><topic>Intestinal Diseases - pathology</topic><topic>Intestinal Diseases - surgery</topic><topic>Metaplasia - metabolism</topic><topic>Metaplasia - pathology</topic><topic>Metaplasia - surgery</topic><topic>Microscopy - instrumentation</topic><topic>Oncology</topic><topic>Optical Imaging</topic><topic>Pathology</topic><topic>Prognosis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mate, Miklos</creatorcontrib><creatorcontrib>Molnar, Bela</creatorcontrib><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>ProQuest Nursing and Allied Health Journals</collection><collection>Immunology Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>ProQuest Health and Medical</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</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</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Nursing &amp; Allied Health Database (Alumni Edition)</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>MEDLINE - Academic</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><jtitle>Pathology oncology research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mate, Miklos</au><au>Molnar, Bela</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A Relation Between Cell Cycle and Intestinal Metaplasia in Oesophageal Biopsies Using Optical and Digital Microscopy</atitle><jtitle>Pathology oncology research</jtitle><stitle>Pathol. Oncol. Res</stitle><addtitle>Pathol Oncol Res</addtitle><date>2015-07-01</date><risdate>2015</risdate><volume>21</volume><issue>3</issue><spage>669</spage><epage>673</epage><pages>669-673</pages><issn>1219-4956</issn><eissn>1532-2807</eissn><abstract>Protein expression changes in relation to cell cycles provide important information, and it may represent a new method for an early diagnosis of metaplasia – dysplasia – adenocarcinoma sequence. We investigated potential changes in cell cycle genes such as protooncogenes (PCNA, EGFR), tumour suppressor gene (p53), apoptotic TUNNEL (Tdt mediated dUTP nick and labelling) gene, as well as small intestinal mucus antigen (SIMA) and large intestinal mucus antigen (LIMA), which accumulates in metaplastic epithelium due to the inflammatory process in routine oesophageal biopsies using immunohistochemistry. Oesophageal biopsies were taken from patients with Barrett’s oesophagus ( n  = 30), reflux oesophagitis ( n  = 30), healthy oesophagus ( n  = 30) and healthy cardia ( n  = 10). Immunohistochemical signalling was carried out by Streptavidin-Biotin-AEC (aminoetil-carbazol). Expression of PCNA was statistically significantly lower in healthy oesophagus ( p  &lt; 0.05) versus reflux oesophagitis and Barrett’s oesophagus. However, no significant change was detected in the expression of SIMA and LIMA in intestinal metaplasia. Further, EGFR, p53 and TUNNEL levels were significantly different in healthy versus Barrett’s oesophagus. Manual counting using virtual microscopy was comparable with the result using conventional light microscopy, but the former is significantly quicker. There was no difference between manual and automated cell counting ( p  &gt; 0.05).</abstract><cop>Dordrecht</cop><pub>Springer Netherlands</pub><pmid>25740071</pmid><doi>10.1007/s12253-014-9873-8</doi><tpages>5</tpages></addata></record>
fulltext fulltext
identifier ISSN: 1219-4956
ispartof Pathology oncology research, 2015-07, Vol.21 (3), p.669-673
issn 1219-4956
1532-2807
language eng
recordid cdi_proquest_miscellaneous_1819147250
source MEDLINE; SpringerLink Journals - AutoHoldings
subjects Barrett Esophagus - metabolism
Barrett Esophagus - pathology
Barrett Esophagus - surgery
Biomarkers - metabolism
Biomedical and Life Sciences
Biomedicine
Biopsy
Cancer Research
Cell Cycle
Esophagus - metabolism
Esophagus - pathology
Esophagus - surgery
Humans
Image Interpretation, Computer-Assisted
Immunoenzyme Techniques
Immunology
Intestinal Diseases - metabolism
Intestinal Diseases - pathology
Intestinal Diseases - surgery
Metaplasia - metabolism
Metaplasia - pathology
Metaplasia - surgery
Microscopy - instrumentation
Oncology
Optical Imaging
Pathology
Prognosis
title A Relation Between Cell Cycle and Intestinal Metaplasia in Oesophageal Biopsies Using Optical and Digital Microscopy
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-14T23%3A56%3A22IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=A%20Relation%20Between%20Cell%20Cycle%20and%20Intestinal%20Metaplasia%20in%20Oesophageal%20Biopsies%20Using%20Optical%20and%20Digital%20Microscopy&rft.jtitle=Pathology%20oncology%20research&rft.au=Mate,%20Miklos&rft.date=2015-07-01&rft.volume=21&rft.issue=3&rft.spage=669&rft.epage=673&rft.pages=669-673&rft.issn=1219-4956&rft.eissn=1532-2807&rft_id=info:doi/10.1007/s12253-014-9873-8&rft_dat=%3Cproquest_cross%3E1819147250%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1685144585&rft_id=info:pmid/25740071&rfr_iscdi=true