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Spindle proteins Aurora A and BUB1B, but not Mad2, are aberrantly expressed in dysplastic mucosa of patients with longstanding ulcerative colitis
Background:Long term ulcerative colitis (UC) increases the risk of colorectal cancer (CRC). DNA aneuploidy is a common feature of both dysplastic and non-dysplastic colonic epithelia from patients with longstanding UC, and is regarded as an early sign of possible malignant transformation. The spindl...
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Published in: | Journal of clinical pathology 2007-12, Vol.60 (12), p.1403-1408 |
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description | Background:Long term ulcerative colitis (UC) increases the risk of colorectal cancer (CRC). DNA aneuploidy is a common feature of both dysplastic and non-dysplastic colonic epithelia from patients with longstanding UC, and is regarded as an early sign of possible malignant transformation. The spindle proteins Aurora A, BUB1B and Mad2 have been implicated as contributors to aneuploidy and carcinogenesis.Aims:To investigate the role of these spindle proteins in relation to DNA aneuploidy and during the progressive morphological changes in ulcerative colitis associated colorectal cancer (UCCRC).Methods:Tissue microarrays were made from 31 colectomy specimens from patients with longstanding UC. Expression of Aurora A, BUB1B and Mad2 was investigated by immunohistochemistry and their relation to ploidy status, mucosal morphology and Ki67 levels was explored.Results:Expression of Aurora A and BUB1B was significantly associated with the progressive morphological changes of UCCRC. In the progression from non-dysplastic to dysplastic mucosa, Aurora A expression decreased while BUB1B expression increased. There was an increasing incidence of aneuploidy with progression towards cancer; expression of all spindle proteins was associated with the level of Ki67 but not with aneuploidy.Conclusion:Due to the significant differences in Aurora A and BUB1B expression in dysplastic compared non-dysplastic mucosa, these proteins may serve as putative biological markers for the progressive morphological changes in UC associated carcinogenesis. The close relationship to Ki67 levels reflect that spindle proteins are expressed in tissues with a high proliferative rate; a role for these proteins in the development of aneuploidy was not found. |
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DNA aneuploidy is a common feature of both dysplastic and non-dysplastic colonic epithelia from patients with longstanding UC, and is regarded as an early sign of possible malignant transformation. The spindle proteins Aurora A, BUB1B and Mad2 have been implicated as contributors to aneuploidy and carcinogenesis.Aims:To investigate the role of these spindle proteins in relation to DNA aneuploidy and during the progressive morphological changes in ulcerative colitis associated colorectal cancer (UCCRC).Methods:Tissue microarrays were made from 31 colectomy specimens from patients with longstanding UC. Expression of Aurora A, BUB1B and Mad2 was investigated by immunohistochemistry and their relation to ploidy status, mucosal morphology and Ki67 levels was explored.Results:Expression of Aurora A and BUB1B was significantly associated with the progressive morphological changes of UCCRC. In the progression from non-dysplastic to dysplastic mucosa, Aurora A expression decreased while BUB1B expression increased. There was an increasing incidence of aneuploidy with progression towards cancer; expression of all spindle proteins was associated with the level of Ki67 but not with aneuploidy.Conclusion:Due to the significant differences in Aurora A and BUB1B expression in dysplastic compared non-dysplastic mucosa, these proteins may serve as putative biological markers for the progressive morphological changes in UC associated carcinogenesis. The close relationship to Ki67 levels reflect that spindle proteins are expressed in tissues with a high proliferative rate; a role for these proteins in the development of aneuploidy was not found.</description><identifier>ISSN: 0021-9746</identifier><identifier>EISSN: 1472-4146</identifier><identifier>DOI: 10.1136/jcp.2006.044305</identifier><identifier>PMID: 17322345</identifier><identifier>CODEN: JCPAAK</identifier><language>eng</language><publisher>England: BMJ Publishing Group Ltd and Association of Clinical Pathologists</publisher><subject>Aurora Kinases ; Biomarkers, Tumor - metabolism ; Calcium-Binding Proteins - metabolism ; Cell Cycle Proteins - metabolism ; Colectomy ; Colitis, Ulcerative - complications ; Colitis, Ulcerative - genetics ; Colitis, Ulcerative - metabolism ; Colitis, Ulcerative - pathology ; Colonic Neoplasms - etiology ; Colonic Neoplasms - genetics ; Colonic Neoplasms - metabolism ; Disease Progression ; DNA, Neoplasm - genetics ; Humans ; Intestinal Mucosa - metabolism ; Ki-67 Antigen - metabolism ; Mad2 Proteins ; Neoplasm Proteins - metabolism ; Original ; Ploidies ; Precancerous Conditions - etiology ; Precancerous Conditions - genetics ; Precancerous Conditions - metabolism ; Protein-Serine-Threonine Kinases - metabolism ; Repressor Proteins - metabolism</subject><ispartof>Journal of clinical pathology, 2007-12, Vol.60 (12), p.1403-1408</ispartof><rights>2007 The BMJ Publishing Group Ltd and the Association of Clinical Pathologists</rights><rights>Copyright: 2007 2007 The BMJ Publishing Group Ltd and the Association of Clinical Pathologists</rights><rights>Copyright © 2007 The BMJ Publishing Group and the Association of Clinical Pathologists</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b492t-b7bcc187273e460727662e5b7f3e1f612de2965eda0cfdde366944913a0423103</citedby><cites>FETCH-LOGICAL-b492t-b7bcc187273e460727662e5b7f3e1f612de2965eda0cfdde366944913a0423103</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2095563/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2095563/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17322345$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Burum-Auensen, E</creatorcontrib><creatorcontrib>DeAngelis, P M</creatorcontrib><creatorcontrib>Schjølberg, A R</creatorcontrib><creatorcontrib>Røislien, Jo</creatorcontrib><creatorcontrib>Andersen, S N</creatorcontrib><creatorcontrib>Clausen, O P F</creatorcontrib><title>Spindle proteins Aurora A and BUB1B, but not Mad2, are aberrantly expressed in dysplastic mucosa of patients with longstanding ulcerative colitis</title><title>Journal of clinical pathology</title><addtitle>J Clin Pathol</addtitle><description>Background:Long term ulcerative colitis (UC) increases the risk of colorectal cancer (CRC). DNA aneuploidy is a common feature of both dysplastic and non-dysplastic colonic epithelia from patients with longstanding UC, and is regarded as an early sign of possible malignant transformation. The spindle proteins Aurora A, BUB1B and Mad2 have been implicated as contributors to aneuploidy and carcinogenesis.Aims:To investigate the role of these spindle proteins in relation to DNA aneuploidy and during the progressive morphological changes in ulcerative colitis associated colorectal cancer (UCCRC).Methods:Tissue microarrays were made from 31 colectomy specimens from patients with longstanding UC. Expression of Aurora A, BUB1B and Mad2 was investigated by immunohistochemistry and their relation to ploidy status, mucosal morphology and Ki67 levels was explored.Results:Expression of Aurora A and BUB1B was significantly associated with the progressive morphological changes of UCCRC. In the progression from non-dysplastic to dysplastic mucosa, Aurora A expression decreased while BUB1B expression increased. There was an increasing incidence of aneuploidy with progression towards cancer; expression of all spindle proteins was associated with the level of Ki67 but not with aneuploidy.Conclusion:Due to the significant differences in Aurora A and BUB1B expression in dysplastic compared non-dysplastic mucosa, these proteins may serve as putative biological markers for the progressive morphological changes in UC associated carcinogenesis. The close relationship to Ki67 levels reflect that spindle proteins are expressed in tissues with a high proliferative rate; a role for these proteins in the development of aneuploidy was not found.</description><subject>Aurora Kinases</subject><subject>Biomarkers, Tumor - metabolism</subject><subject>Calcium-Binding Proteins - metabolism</subject><subject>Cell Cycle Proteins - metabolism</subject><subject>Colectomy</subject><subject>Colitis, Ulcerative - complications</subject><subject>Colitis, Ulcerative - genetics</subject><subject>Colitis, Ulcerative - metabolism</subject><subject>Colitis, Ulcerative - pathology</subject><subject>Colonic Neoplasms - etiology</subject><subject>Colonic Neoplasms - genetics</subject><subject>Colonic Neoplasms - metabolism</subject><subject>Disease Progression</subject><subject>DNA, Neoplasm - genetics</subject><subject>Humans</subject><subject>Intestinal Mucosa - metabolism</subject><subject>Ki-67 Antigen - metabolism</subject><subject>Mad2 Proteins</subject><subject>Neoplasm Proteins - metabolism</subject><subject>Original</subject><subject>Ploidies</subject><subject>Precancerous Conditions - etiology</subject><subject>Precancerous Conditions - genetics</subject><subject>Precancerous Conditions - metabolism</subject><subject>Protein-Serine-Threonine Kinases - metabolism</subject><subject>Repressor Proteins - metabolism</subject><issn>0021-9746</issn><issn>1472-4146</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><recordid>eNqFkU9vEzEUxFcIREvhzA1Z4oa6qf-tnb0gJREQRIBDaa-W1_s2ddjYi-0tzcfgG-NqowInTnOY35s30hTFS4JnhDBxsTPDjGIsZphzhqtHxSnhkpaccPG4OMWYkrKWXJwUz2LcYUyYJOxpcUIko5Tx6rT4dTlY1_aAhuATWBfRYgw-aLRA2rVoebUky3PUjAk5n9Bn3dJzpAMg3UAI2qX-gOBuCBAjtMg61B7i0OuYrEH70fioke_QoJMFlyL6adMN6r3bxpTTrduisTcQsn0LyPjeJhufF0863Ud4cdSz4ur9u2-rdbn5-uHjarEpG17TVDayMYbMJZUMuMBZhaBQNbJjQDpBaAu0FhW0GpuubYEJUXNeE6Yxp4xgdla8nXKHsdlDa3LBoHs1BLvX4aC8tupfx9kbtfW3iuK6qgTLAa-PAcH_GCEmtfNjcLmzInJOMJ1P1MVEmeBjDNA9fCBY3W-o8obqfkM1bZgvXv1d7A9_HC0D5QTYmODuwdfhuxKSyUp9uV4puf50eb3arBXN_JuJb_a7_37_DQOgtfg</recordid><startdate>20071201</startdate><enddate>20071201</enddate><creator>Burum-Auensen, E</creator><creator>DeAngelis, P M</creator><creator>Schjølberg, A R</creator><creator>Røislien, Jo</creator><creator>Andersen, S N</creator><creator>Clausen, O P F</creator><general>BMJ Publishing Group Ltd and Association of Clinical Pathologists</general><general>BMJ Publishing Group LTD</general><general>BMJ Group</general><scope>BSCLL</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>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88I</scope><scope>8AF</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>BTHHO</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>5PM</scope></search><sort><creationdate>20071201</creationdate><title>Spindle proteins Aurora A and BUB1B, but not Mad2, are aberrantly expressed in dysplastic mucosa of patients with longstanding ulcerative colitis</title><author>Burum-Auensen, E ; DeAngelis, P M ; Schjølberg, A R ; Røislien, Jo ; Andersen, S N ; Clausen, O P F</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b492t-b7bcc187273e460727662e5b7f3e1f612de2965eda0cfdde366944913a0423103</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Aurora Kinases</topic><topic>Biomarkers, Tumor - metabolism</topic><topic>Calcium-Binding Proteins - metabolism</topic><topic>Cell Cycle Proteins - metabolism</topic><topic>Colectomy</topic><topic>Colitis, Ulcerative - complications</topic><topic>Colitis, Ulcerative - genetics</topic><topic>Colitis, Ulcerative - metabolism</topic><topic>Colitis, Ulcerative - pathology</topic><topic>Colonic Neoplasms - etiology</topic><topic>Colonic Neoplasms - genetics</topic><topic>Colonic Neoplasms - metabolism</topic><topic>Disease Progression</topic><topic>DNA, Neoplasm - genetics</topic><topic>Humans</topic><topic>Intestinal Mucosa - metabolism</topic><topic>Ki-67 Antigen - metabolism</topic><topic>Mad2 Proteins</topic><topic>Neoplasm Proteins - metabolism</topic><topic>Original</topic><topic>Ploidies</topic><topic>Precancerous Conditions - etiology</topic><topic>Precancerous Conditions - genetics</topic><topic>Precancerous Conditions - metabolism</topic><topic>Protein-Serine-Threonine Kinases - metabolism</topic><topic>Repressor Proteins - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Burum-Auensen, E</creatorcontrib><creatorcontrib>DeAngelis, P M</creatorcontrib><creatorcontrib>Schjølberg, A R</creatorcontrib><creatorcontrib>Røislien, Jo</creatorcontrib><creatorcontrib>Andersen, S N</creatorcontrib><creatorcontrib>Clausen, O P F</creatorcontrib><collection>Istex</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>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>STEM Database</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)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>BMJ Journals</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>ProQuest Science Journals</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>ProQuest Central Basic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of clinical pathology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Burum-Auensen, E</au><au>DeAngelis, P M</au><au>Schjølberg, A R</au><au>Røislien, Jo</au><au>Andersen, S N</au><au>Clausen, O P F</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Spindle proteins Aurora A and BUB1B, but not Mad2, are aberrantly expressed in dysplastic mucosa of patients with longstanding ulcerative colitis</atitle><jtitle>Journal of clinical pathology</jtitle><addtitle>J Clin Pathol</addtitle><date>2007-12-01</date><risdate>2007</risdate><volume>60</volume><issue>12</issue><spage>1403</spage><epage>1408</epage><pages>1403-1408</pages><issn>0021-9746</issn><eissn>1472-4146</eissn><coden>JCPAAK</coden><abstract>Background:Long term ulcerative colitis (UC) increases the risk of colorectal cancer (CRC). DNA aneuploidy is a common feature of both dysplastic and non-dysplastic colonic epithelia from patients with longstanding UC, and is regarded as an early sign of possible malignant transformation. The spindle proteins Aurora A, BUB1B and Mad2 have been implicated as contributors to aneuploidy and carcinogenesis.Aims:To investigate the role of these spindle proteins in relation to DNA aneuploidy and during the progressive morphological changes in ulcerative colitis associated colorectal cancer (UCCRC).Methods:Tissue microarrays were made from 31 colectomy specimens from patients with longstanding UC. Expression of Aurora A, BUB1B and Mad2 was investigated by immunohistochemistry and their relation to ploidy status, mucosal morphology and Ki67 levels was explored.Results:Expression of Aurora A and BUB1B was significantly associated with the progressive morphological changes of UCCRC. In the progression from non-dysplastic to dysplastic mucosa, Aurora A expression decreased while BUB1B expression increased. There was an increasing incidence of aneuploidy with progression towards cancer; expression of all spindle proteins was associated with the level of Ki67 but not with aneuploidy.Conclusion:Due to the significant differences in Aurora A and BUB1B expression in dysplastic compared non-dysplastic mucosa, these proteins may serve as putative biological markers for the progressive morphological changes in UC associated carcinogenesis. The close relationship to Ki67 levels reflect that spindle proteins are expressed in tissues with a high proliferative rate; a role for these proteins in the development of aneuploidy was not found.</abstract><cop>England</cop><pub>BMJ Publishing Group Ltd and Association of Clinical Pathologists</pub><pmid>17322345</pmid><doi>10.1136/jcp.2006.044305</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Aurora Kinases Biomarkers, Tumor - metabolism Calcium-Binding Proteins - metabolism Cell Cycle Proteins - metabolism Colectomy Colitis, Ulcerative - complications Colitis, Ulcerative - genetics Colitis, Ulcerative - metabolism Colitis, Ulcerative - pathology Colonic Neoplasms - etiology Colonic Neoplasms - genetics Colonic Neoplasms - metabolism Disease Progression DNA, Neoplasm - genetics Humans Intestinal Mucosa - metabolism Ki-67 Antigen - metabolism Mad2 Proteins Neoplasm Proteins - metabolism Original Ploidies Precancerous Conditions - etiology Precancerous Conditions - genetics Precancerous Conditions - metabolism Protein-Serine-Threonine Kinases - metabolism Repressor Proteins - metabolism |
title | Spindle proteins Aurora A and BUB1B, but not Mad2, are aberrantly expressed in dysplastic mucosa of patients with longstanding ulcerative colitis |
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