Loading…

Polypeptide expression in prostate hyperplasia and prostate adenocarcinoma

Cells were collected from prostate hyperplasias (n = 6) and prostate carcinomas (n = 6) and subjected to two-dimensional gel electrophoresis (2-DE). The resulting polypeptide patterns were analysed with the PDQUEST computer software. Malignant tumors showed significant increases in the level of expr...

Full description

Saved in:
Bibliographic Details
Published in:Analytical cellular pathology 2000, Vol.21 (1), p.1-9
Main Authors: Alaiya, A, Roblick, U, Egevad, L, Carlsson, A, Franzén, B, Volz, D, Huwendiek, S, Linder, S, Auer, G
Format: Article
Language:English
Subjects:
Citations: Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c481t-974ce6dde2cc33f9bf6e32a47c9b62c6fd6b1b8b2539e04f285c043f4ff20a343
cites
container_end_page 9
container_issue 1
container_start_page 1
container_title Analytical cellular pathology
container_volume 21
creator Alaiya, A
Roblick, U
Egevad, L
Carlsson, A
Franzén, B
Volz, D
Huwendiek, S
Linder, S
Auer, G
description Cells were collected from prostate hyperplasias (n = 6) and prostate carcinomas (n = 6) and subjected to two-dimensional gel electrophoresis (2-DE). The resulting polypeptide patterns were analysed with the PDQUEST computer software. Malignant tumors showed significant increases in the level of expression of proliferating cell nuclear antigen (PCNA), calreticulin, HSP 90 and pHSP 60, oncoprotein 18(v), elongation factor 2, glutathione-S-transferase pi (GST-pi), superoxide dismutase and triose phosphate isomerase. In addition, decreases in the levels of tropomyosin-1 and 2 and cytokeratin 18 were observed in prostate carcinomas compared to prostate hyperplasias. This pattern of alterations is similar to that observed in other carcinomas in our previous studies. All malignant tumors showed simultaneous alterations in 5 or more of 9 markers studied, whereas only one case of benign hyperplasia showed alterations in 5 markers. The EST-data base for prostate tumors available from NCI (CGAP) was searched for the expression of the mRNAs corresponding to proteins identified in our gels. Large differences in the relative expression of mRNAs and proteins were observed. Our data show alterations in the pattem of polypeptide expression in prostate carcinomas which are similar to those observed in other carcinomas.
doi_str_mv 10.1155/2000/351963
format article
fullrecord <record><control><sourceid>proquest_doaj_</sourceid><recordid>TN_cdi_doaj_primary_oai_doaj_org_article_f703c4ae00e5454b8054940be80f1a87</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><doaj_id>oai_doaj_org_article_f703c4ae00e5454b8054940be80f1a87</doaj_id><sourcerecordid>72580867</sourcerecordid><originalsourceid>FETCH-LOGICAL-c481t-974ce6dde2cc33f9bf6e32a47c9b62c6fd6b1b8b2539e04f285c043f4ff20a343</originalsourceid><addsrcrecordid>eNpVkUFv1DAQRi0EokvhxB3lxAWFjsd24lyQUEWhqBIc4Gw5zrh1ycbBzgL99_WSFWVPtmae34z8MfaSw1vOlTpDADgTineNeMQ2iBzqlmv1mG2gQ17rjuMJe5bzLQBHjfCUnXCOSiLChn3-Gse7meYlDFTRnzlRziFOVZiqOcW82IWqmwKkebQ52MpOw0PDDjRFZ5MLU9za5-yJt2OmF4fzlH2_-PDt_FN99eXj5fn7q9pJzZe6a6WjZhgInRPCd71vSKCVrev6Bl3jh6bnve5RiY5AetTKgRReeo9ghRSn7HL1DtHemjmFrU13Jtpg_hZiujY2LcGNZHwLwklLAKSkkr0GJTsJPWnw3Oq2uOrVlX_TvOuPbIfSj3IjozpdXIV_t_Kls6XB0bQkOx49O-5M4cZcx19GNlxLhCJ4fRCk-HNHeTHbkB2No50o7rJpUWnQzX6zNyvoym_nRP7fEA5mn7vZ527W3Av96v-9HthD0OIeHBSqMA</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>72580867</pqid></control><display><type>article</type><title>Polypeptide expression in prostate hyperplasia and prostate adenocarcinoma</title><source>Wiley Online Library Open Access</source><source>PubMed Central</source><creator>Alaiya, A ; Roblick, U ; Egevad, L ; Carlsson, A ; Franzén, B ; Volz, D ; Huwendiek, S ; Linder, S ; Auer, G</creator><creatorcontrib>Alaiya, A ; Roblick, U ; Egevad, L ; Carlsson, A ; Franzén, B ; Volz, D ; Huwendiek, S ; Linder, S ; Auer, G</creatorcontrib><description>Cells were collected from prostate hyperplasias (n = 6) and prostate carcinomas (n = 6) and subjected to two-dimensional gel electrophoresis (2-DE). The resulting polypeptide patterns were analysed with the PDQUEST computer software. Malignant tumors showed significant increases in the level of expression of proliferating cell nuclear antigen (PCNA), calreticulin, HSP 90 and pHSP 60, oncoprotein 18(v), elongation factor 2, glutathione-S-transferase pi (GST-pi), superoxide dismutase and triose phosphate isomerase. In addition, decreases in the levels of tropomyosin-1 and 2 and cytokeratin 18 were observed in prostate carcinomas compared to prostate hyperplasias. This pattern of alterations is similar to that observed in other carcinomas in our previous studies. All malignant tumors showed simultaneous alterations in 5 or more of 9 markers studied, whereas only one case of benign hyperplasia showed alterations in 5 markers. The EST-data base for prostate tumors available from NCI (CGAP) was searched for the expression of the mRNAs corresponding to proteins identified in our gels. Large differences in the relative expression of mRNAs and proteins were observed. Our data show alterations in the pattem of polypeptide expression in prostate carcinomas which are similar to those observed in other carcinomas.</description><identifier>ISSN: 0921-8912</identifier><identifier>ISSN: 2210-7177</identifier><identifier>EISSN: 2210-7185</identifier><identifier>EISSN: 1878-3651</identifier><identifier>DOI: 10.1155/2000/351963</identifier><identifier>PMID: 11254220</identifier><language>eng</language><publisher>Netherlands: IOS Press</publisher><subject>Adenocarcinoma - genetics ; Adenocarcinoma - metabolism ; Aged ; Aged, 80 and over ; Biomarkers, Tumor - biosynthesis ; Biomarkers, Tumor - genetics ; Cell Differentiation ; Electrophoresis, Gel, Two-Dimensional ; Gene Expression Profiling - methods ; Gene Expression Regulation, Neoplastic ; Humans ; Image Processing, Computer-Assisted ; Male ; Middle Aged ; Neoplasm Proteins - biosynthesis ; Neoplasm Proteins - genetics ; Other ; Prostatic Hyperplasia - genetics ; Prostatic Hyperplasia - metabolism ; Prostatic Neoplasms - genetics ; Prostatic Neoplasms - metabolism</subject><ispartof>Analytical cellular pathology, 2000, Vol.21 (1), p.1-9</ispartof><rights>Copyright © 2000 Hindawi Publishing Corporation. 2000</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c481t-974ce6dde2cc33f9bf6e32a47c9b62c6fd6b1b8b2539e04f285c043f4ff20a343</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4618420/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4618420/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,4010,27900,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11254220$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttp://kipublications.ki.se/Default.aspx?queryparsed=id:1949060$$DView record from Swedish Publication Index$$Hfree_for_read</backlink></links><search><creatorcontrib>Alaiya, A</creatorcontrib><creatorcontrib>Roblick, U</creatorcontrib><creatorcontrib>Egevad, L</creatorcontrib><creatorcontrib>Carlsson, A</creatorcontrib><creatorcontrib>Franzén, B</creatorcontrib><creatorcontrib>Volz, D</creatorcontrib><creatorcontrib>Huwendiek, S</creatorcontrib><creatorcontrib>Linder, S</creatorcontrib><creatorcontrib>Auer, G</creatorcontrib><title>Polypeptide expression in prostate hyperplasia and prostate adenocarcinoma</title><title>Analytical cellular pathology</title><addtitle>Anal Cell Pathol</addtitle><description>Cells were collected from prostate hyperplasias (n = 6) and prostate carcinomas (n = 6) and subjected to two-dimensional gel electrophoresis (2-DE). The resulting polypeptide patterns were analysed with the PDQUEST computer software. Malignant tumors showed significant increases in the level of expression of proliferating cell nuclear antigen (PCNA), calreticulin, HSP 90 and pHSP 60, oncoprotein 18(v), elongation factor 2, glutathione-S-transferase pi (GST-pi), superoxide dismutase and triose phosphate isomerase. In addition, decreases in the levels of tropomyosin-1 and 2 and cytokeratin 18 were observed in prostate carcinomas compared to prostate hyperplasias. This pattern of alterations is similar to that observed in other carcinomas in our previous studies. All malignant tumors showed simultaneous alterations in 5 or more of 9 markers studied, whereas only one case of benign hyperplasia showed alterations in 5 markers. The EST-data base for prostate tumors available from NCI (CGAP) was searched for the expression of the mRNAs corresponding to proteins identified in our gels. Large differences in the relative expression of mRNAs and proteins were observed. Our data show alterations in the pattem of polypeptide expression in prostate carcinomas which are similar to those observed in other carcinomas.</description><subject>Adenocarcinoma - genetics</subject><subject>Adenocarcinoma - metabolism</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Biomarkers, Tumor - biosynthesis</subject><subject>Biomarkers, Tumor - genetics</subject><subject>Cell Differentiation</subject><subject>Electrophoresis, Gel, Two-Dimensional</subject><subject>Gene Expression Profiling - methods</subject><subject>Gene Expression Regulation, Neoplastic</subject><subject>Humans</subject><subject>Image Processing, Computer-Assisted</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Neoplasm Proteins - biosynthesis</subject><subject>Neoplasm Proteins - genetics</subject><subject>Other</subject><subject>Prostatic Hyperplasia - genetics</subject><subject>Prostatic Hyperplasia - metabolism</subject><subject>Prostatic Neoplasms - genetics</subject><subject>Prostatic Neoplasms - metabolism</subject><issn>0921-8912</issn><issn>2210-7177</issn><issn>2210-7185</issn><issn>1878-3651</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2000</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNpVkUFv1DAQRi0EokvhxB3lxAWFjsd24lyQUEWhqBIc4Gw5zrh1ycbBzgL99_WSFWVPtmae34z8MfaSw1vOlTpDADgTineNeMQ2iBzqlmv1mG2gQ17rjuMJe5bzLQBHjfCUnXCOSiLChn3-Gse7meYlDFTRnzlRziFOVZiqOcW82IWqmwKkebQ52MpOw0PDDjRFZ5MLU9za5-yJt2OmF4fzlH2_-PDt_FN99eXj5fn7q9pJzZe6a6WjZhgInRPCd71vSKCVrev6Bl3jh6bnve5RiY5AetTKgRReeo9ghRSn7HL1DtHemjmFrU13Jtpg_hZiujY2LcGNZHwLwklLAKSkkr0GJTsJPWnw3Oq2uOrVlX_TvOuPbIfSj3IjozpdXIV_t_Kls6XB0bQkOx49O-5M4cZcx19GNlxLhCJ4fRCk-HNHeTHbkB2No50o7rJpUWnQzX6zNyvoym_nRP7fEA5mn7vZ527W3Av96v-9HthD0OIeHBSqMA</recordid><startdate>2000</startdate><enddate>2000</enddate><creator>Alaiya, A</creator><creator>Roblick, U</creator><creator>Egevad, L</creator><creator>Carlsson, A</creator><creator>Franzén, B</creator><creator>Volz, D</creator><creator>Huwendiek, S</creator><creator>Linder, S</creator><creator>Auer, G</creator><general>IOS Press</general><general>Hindawi Limited</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>7X8</scope><scope>5PM</scope><scope>ADTPV</scope><scope>AOWAS</scope><scope>D8T</scope><scope>ZZAVC</scope><scope>DOA</scope></search><sort><creationdate>2000</creationdate><title>Polypeptide expression in prostate hyperplasia and prostate adenocarcinoma</title><author>Alaiya, A ; Roblick, U ; Egevad, L ; Carlsson, A ; Franzén, B ; Volz, D ; Huwendiek, S ; Linder, S ; Auer, G</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c481t-974ce6dde2cc33f9bf6e32a47c9b62c6fd6b1b8b2539e04f285c043f4ff20a343</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2000</creationdate><topic>Adenocarcinoma - genetics</topic><topic>Adenocarcinoma - metabolism</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Biomarkers, Tumor - biosynthesis</topic><topic>Biomarkers, Tumor - genetics</topic><topic>Cell Differentiation</topic><topic>Electrophoresis, Gel, Two-Dimensional</topic><topic>Gene Expression Profiling - methods</topic><topic>Gene Expression Regulation, Neoplastic</topic><topic>Humans</topic><topic>Image Processing, Computer-Assisted</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Neoplasm Proteins - biosynthesis</topic><topic>Neoplasm Proteins - genetics</topic><topic>Other</topic><topic>Prostatic Hyperplasia - genetics</topic><topic>Prostatic Hyperplasia - metabolism</topic><topic>Prostatic Neoplasms - genetics</topic><topic>Prostatic Neoplasms - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Alaiya, A</creatorcontrib><creatorcontrib>Roblick, U</creatorcontrib><creatorcontrib>Egevad, L</creatorcontrib><creatorcontrib>Carlsson, A</creatorcontrib><creatorcontrib>Franzén, B</creatorcontrib><creatorcontrib>Volz, D</creatorcontrib><creatorcontrib>Huwendiek, S</creatorcontrib><creatorcontrib>Linder, S</creatorcontrib><creatorcontrib>Auer, G</creatorcontrib><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>PubMed Central (Full Participant titles)</collection><collection>SwePub</collection><collection>SwePub Articles</collection><collection>SWEPUB Freely available online</collection><collection>SwePub Articles full text</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Analytical cellular pathology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Alaiya, A</au><au>Roblick, U</au><au>Egevad, L</au><au>Carlsson, A</au><au>Franzén, B</au><au>Volz, D</au><au>Huwendiek, S</au><au>Linder, S</au><au>Auer, G</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Polypeptide expression in prostate hyperplasia and prostate adenocarcinoma</atitle><jtitle>Analytical cellular pathology</jtitle><addtitle>Anal Cell Pathol</addtitle><date>2000</date><risdate>2000</risdate><volume>21</volume><issue>1</issue><spage>1</spage><epage>9</epage><pages>1-9</pages><issn>0921-8912</issn><issn>2210-7177</issn><eissn>2210-7185</eissn><eissn>1878-3651</eissn><abstract>Cells were collected from prostate hyperplasias (n = 6) and prostate carcinomas (n = 6) and subjected to two-dimensional gel electrophoresis (2-DE). The resulting polypeptide patterns were analysed with the PDQUEST computer software. Malignant tumors showed significant increases in the level of expression of proliferating cell nuclear antigen (PCNA), calreticulin, HSP 90 and pHSP 60, oncoprotein 18(v), elongation factor 2, glutathione-S-transferase pi (GST-pi), superoxide dismutase and triose phosphate isomerase. In addition, decreases in the levels of tropomyosin-1 and 2 and cytokeratin 18 were observed in prostate carcinomas compared to prostate hyperplasias. This pattern of alterations is similar to that observed in other carcinomas in our previous studies. All malignant tumors showed simultaneous alterations in 5 or more of 9 markers studied, whereas only one case of benign hyperplasia showed alterations in 5 markers. The EST-data base for prostate tumors available from NCI (CGAP) was searched for the expression of the mRNAs corresponding to proteins identified in our gels. Large differences in the relative expression of mRNAs and proteins were observed. Our data show alterations in the pattem of polypeptide expression in prostate carcinomas which are similar to those observed in other carcinomas.</abstract><cop>Netherlands</cop><pub>IOS Press</pub><pmid>11254220</pmid><doi>10.1155/2000/351963</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0921-8912
ispartof Analytical cellular pathology, 2000, Vol.21 (1), p.1-9
issn 0921-8912
2210-7177
2210-7185
1878-3651
language eng
recordid cdi_doaj_primary_oai_doaj_org_article_f703c4ae00e5454b8054940be80f1a87
source Wiley Online Library Open Access; PubMed Central
subjects Adenocarcinoma - genetics
Adenocarcinoma - metabolism
Aged
Aged, 80 and over
Biomarkers, Tumor - biosynthesis
Biomarkers, Tumor - genetics
Cell Differentiation
Electrophoresis, Gel, Two-Dimensional
Gene Expression Profiling - methods
Gene Expression Regulation, Neoplastic
Humans
Image Processing, Computer-Assisted
Male
Middle Aged
Neoplasm Proteins - biosynthesis
Neoplasm Proteins - genetics
Other
Prostatic Hyperplasia - genetics
Prostatic Hyperplasia - metabolism
Prostatic Neoplasms - genetics
Prostatic Neoplasms - metabolism
title Polypeptide expression in prostate hyperplasia and prostate adenocarcinoma
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-30T06%3A59%3A12IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_doaj_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Polypeptide%20expression%20in%20prostate%20hyperplasia%20and%20prostate%20adenocarcinoma&rft.jtitle=Analytical%20cellular%20pathology&rft.au=Alaiya,%20A&rft.date=2000&rft.volume=21&rft.issue=1&rft.spage=1&rft.epage=9&rft.pages=1-9&rft.issn=0921-8912&rft.eissn=2210-7185&rft_id=info:doi/10.1155/2000/351963&rft_dat=%3Cproquest_doaj_%3E72580867%3C/proquest_doaj_%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c481t-974ce6dde2cc33f9bf6e32a47c9b62c6fd6b1b8b2539e04f285c043f4ff20a343%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=72580867&rft_id=info:pmid/11254220&rfr_iscdi=true