Does human papillomavirus play a role in the development of bladder transitional cell carcinoma? A comparison of PCR and immunohistochemical analysis

Aim: To investigate the role of human papillomavirus (HPV) in the development of bladder transitional cell carcinoma (TCC). Methods: Seventy eight paraffin wax embedded TCC samples were tested for the presence of HPV by two methods. First, immunohistochemistry was carried out using a polyclonal anti...

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Veröffentlicht in:Journal of clinical pathology 2005-02, Vol.58 (2), p.207-210
Hauptverfasser: Youshya, S, Purdie, K, Breuer, J, Proby, C, Sheaf, M T, Oliver, R T D, Baithun, S
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container_issue 2
container_start_page 207
container_title Journal of clinical pathology
container_volume 58
creator Youshya, S
Purdie, K
Breuer, J
Proby, C
Sheaf, M T
Oliver, R T D
Baithun, S
description Aim: To investigate the role of human papillomavirus (HPV) in the development of bladder transitional cell carcinoma (TCC). Methods: Seventy eight paraffin wax embedded TCC samples were tested for the presence of HPV by two methods. First, immunohistochemistry was carried out using a polyclonal antibody capable of detecting the capsid protein of all known papillomaviruses. The second method was a consensus GP5+/6+ primer mediated polymerase chain reaction (PCR) technique, with the products analysed by both agarose gel electrophoresis and an enzyme immunoassay using type specific oligonucleotide probes for 10 different mucosal genotypes. To exclude false negative results because of the poor quality of DNA extracted from paraffin wax embedded samples, the series was extended to include 20 further blocks for which the corresponding snap frozen unfixed tissue was available. Results: The two methods produced contrasting results, with 47 of the 78 samples positive for HPV antigen and none positive for HPV DNA. HPV DNA was not detected in the 20 additional paraffin wax embedded TCCs or in the 20 paired unfixed samples. In contrast, HPV DNA was amplified by PCR from all six of the paraffin wax embedded cervical carcinoma and anogenital wart control samples. Conclusion: The disparity between the two sets of results is probably caused by false positives resulting from the non-specificity of the polyclonal antibody used for immunohistochemistry. These results suggest that HPV is unlikely to play an aetiological role in the development of bladder TCC.
doi_str_mv 10.1136/jcp.2004.017152
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A comparison of PCR and immunohistochemical analysis</title><source>MEDLINE</source><source>EZB-FREE-00999 freely available EZB journals</source><source>PubMed Central</source><source>Alma/SFX Local Collection</source><creator>Youshya, S ; Purdie, K ; Breuer, J ; Proby, C ; Sheaf, M T ; Oliver, R T D ; Baithun, S</creator><creatorcontrib>Youshya, S ; Purdie, K ; Breuer, J ; Proby, C ; Sheaf, M T ; Oliver, R T D ; Baithun, S</creatorcontrib><description>Aim: To investigate the role of human papillomavirus (HPV) in the development of bladder transitional cell carcinoma (TCC). Methods: Seventy eight paraffin wax embedded TCC samples were tested for the presence of HPV by two methods. First, immunohistochemistry was carried out using a polyclonal antibody capable of detecting the capsid protein of all known papillomaviruses. The second method was a consensus GP5+/6+ primer mediated polymerase chain reaction (PCR) technique, with the products analysed by both agarose gel electrophoresis and an enzyme immunoassay using type specific oligonucleotide probes for 10 different mucosal genotypes. To exclude false negative results because of the poor quality of DNA extracted from paraffin wax embedded samples, the series was extended to include 20 further blocks for which the corresponding snap frozen unfixed tissue was available. Results: The two methods produced contrasting results, with 47 of the 78 samples positive for HPV antigen and none positive for HPV DNA. HPV DNA was not detected in the 20 additional paraffin wax embedded TCCs or in the 20 paired unfixed samples. In contrast, HPV DNA was amplified by PCR from all six of the paraffin wax embedded cervical carcinoma and anogenital wart control samples. Conclusion: The disparity between the two sets of results is probably caused by false positives resulting from the non-specificity of the polyclonal antibody used for immunohistochemistry. These results suggest that HPV is unlikely to play an aetiological role in the development of bladder TCC.</description><identifier>ISSN: 0021-9746</identifier><identifier>EISSN: 1472-4146</identifier><identifier>DOI: 10.1136/jcp.2004.017152</identifier><identifier>PMID: 15677544</identifier><identifier>CODEN: JCPAAK</identifier><language>eng</language><publisher>London: BMJ Publishing Group Ltd and Association of Clinical Pathologists</publisher><subject>Adult ; Aged ; Aged, 80 and over ; Antibodies, Viral - analysis ; Antibody Specificity - immunology ; Antigens ; Antigens, Viral - analysis ; Biological and medical sciences ; Biopsy ; Bladder ; bladder cancer ; Capsid Proteins - analysis ; Carcinoma, Transitional Cell - immunology ; Carcinoma, Transitional Cell - virology ; Cervical cancer ; Deoxyribonucleic acid ; DIG ; digoxigenin ; DNA ; DNA, Viral - analysis ; EIA ; enzyme immunoassay ; enzyme immunoassay-polymerase chain reaction ; Enzymes ; Genetic testing ; HPV ; Human papillomavirus ; human papillomavirus antibody ; Humans ; Immunoassay ; Immunohistochemistry - methods ; Infections ; Investigative techniques, diagnostic techniques (general aspects) ; Medical sciences ; Middle Aged ; Nephrology. Urinary tract diseases ; Original ; Papillomaviridae - immunology ; Papillomaviridae - isolation &amp; purification ; papillomavirus ; Papillomavirus Infections - complications ; Papillomavirus Infections - immunology ; Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques ; PCR ; Plasmids ; Polyclonal antibodies ; Polymerase chain reaction ; Polymerase Chain Reaction - methods ; Studies ; TCC ; transitional cell carcinoma ; Tumors ; Tumors of the urinary system ; Urinary Bladder Neoplasms - immunology ; Urinary Bladder Neoplasms - virology ; Urinary tract. Prostate gland</subject><ispartof>Journal of clinical pathology, 2005-02, Vol.58 (2), p.207-210</ispartof><rights>Copyright 2005 Journal of Clinical Pathology</rights><rights>2005 INIST-CNRS</rights><rights>Copyright: 2005 Copyright 2005 Journal of Clinical Pathology</rights><rights>Copyright © Copyright 2005 Journal of Clinical Pathology 2005</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b588t-c6c1291e21ed9a4c58265f3d6482e820800e8a7b444e6e12960f6772d373bcce3</citedby><cites>FETCH-LOGICAL-b588t-c6c1291e21ed9a4c58265f3d6482e820800e8a7b444e6e12960f6772d373bcce3</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/PMC1770580/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1770580/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=16484113$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15677544$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Youshya, S</creatorcontrib><creatorcontrib>Purdie, K</creatorcontrib><creatorcontrib>Breuer, J</creatorcontrib><creatorcontrib>Proby, C</creatorcontrib><creatorcontrib>Sheaf, M T</creatorcontrib><creatorcontrib>Oliver, R T D</creatorcontrib><creatorcontrib>Baithun, S</creatorcontrib><title>Does human papillomavirus play a role in the development of bladder transitional cell carcinoma? A comparison of PCR and immunohistochemical analysis</title><title>Journal of clinical pathology</title><addtitle>J Clin Pathol</addtitle><description>Aim: To investigate the role of human papillomavirus (HPV) in the development of bladder transitional cell carcinoma (TCC). Methods: Seventy eight paraffin wax embedded TCC samples were tested for the presence of HPV by two methods. First, immunohistochemistry was carried out using a polyclonal antibody capable of detecting the capsid protein of all known papillomaviruses. The second method was a consensus GP5+/6+ primer mediated polymerase chain reaction (PCR) technique, with the products analysed by both agarose gel electrophoresis and an enzyme immunoassay using type specific oligonucleotide probes for 10 different mucosal genotypes. To exclude false negative results because of the poor quality of DNA extracted from paraffin wax embedded samples, the series was extended to include 20 further blocks for which the corresponding snap frozen unfixed tissue was available. Results: The two methods produced contrasting results, with 47 of the 78 samples positive for HPV antigen and none positive for HPV DNA. HPV DNA was not detected in the 20 additional paraffin wax embedded TCCs or in the 20 paired unfixed samples. In contrast, HPV DNA was amplified by PCR from all six of the paraffin wax embedded cervical carcinoma and anogenital wart control samples. Conclusion: The disparity between the two sets of results is probably caused by false positives resulting from the non-specificity of the polyclonal antibody used for immunohistochemistry. These results suggest that HPV is unlikely to play an aetiological role in the development of bladder TCC.</description><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Antibodies, Viral - analysis</subject><subject>Antibody Specificity - immunology</subject><subject>Antigens</subject><subject>Antigens, Viral - analysis</subject><subject>Biological and medical sciences</subject><subject>Biopsy</subject><subject>Bladder</subject><subject>bladder cancer</subject><subject>Capsid Proteins - analysis</subject><subject>Carcinoma, Transitional Cell - immunology</subject><subject>Carcinoma, Transitional Cell - virology</subject><subject>Cervical cancer</subject><subject>Deoxyribonucleic acid</subject><subject>DIG</subject><subject>digoxigenin</subject><subject>DNA</subject><subject>DNA, Viral - analysis</subject><subject>EIA</subject><subject>enzyme immunoassay</subject><subject>enzyme immunoassay-polymerase chain reaction</subject><subject>Enzymes</subject><subject>Genetic testing</subject><subject>HPV</subject><subject>Human papillomavirus</subject><subject>human papillomavirus antibody</subject><subject>Humans</subject><subject>Immunoassay</subject><subject>Immunohistochemistry - methods</subject><subject>Infections</subject><subject>Investigative techniques, diagnostic techniques (general aspects)</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Nephrology. Urinary tract diseases</subject><subject>Original</subject><subject>Papillomaviridae - immunology</subject><subject>Papillomaviridae - isolation &amp; purification</subject><subject>papillomavirus</subject><subject>Papillomavirus Infections - complications</subject><subject>Papillomavirus Infections - immunology</subject><subject>Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques</subject><subject>PCR</subject><subject>Plasmids</subject><subject>Polyclonal antibodies</subject><subject>Polymerase chain reaction</subject><subject>Polymerase Chain Reaction - methods</subject><subject>Studies</subject><subject>TCC</subject><subject>transitional cell carcinoma</subject><subject>Tumors</subject><subject>Tumors of the urinary system</subject><subject>Urinary Bladder Neoplasms - immunology</subject><subject>Urinary Bladder Neoplasms - virology</subject><subject>Urinary tract. 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A comparison of PCR and immunohistochemical analysis</title><author>Youshya, S ; Purdie, K ; Breuer, J ; Proby, C ; Sheaf, M T ; Oliver, R T D ; Baithun, S</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b588t-c6c1291e21ed9a4c58265f3d6482e820800e8a7b444e6e12960f6772d373bcce3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Antibodies, Viral - analysis</topic><topic>Antibody Specificity - immunology</topic><topic>Antigens</topic><topic>Antigens, Viral - analysis</topic><topic>Biological and medical sciences</topic><topic>Biopsy</topic><topic>Bladder</topic><topic>bladder cancer</topic><topic>Capsid Proteins - analysis</topic><topic>Carcinoma, Transitional Cell - immunology</topic><topic>Carcinoma, Transitional Cell - virology</topic><topic>Cervical cancer</topic><topic>Deoxyribonucleic acid</topic><topic>DIG</topic><topic>digoxigenin</topic><topic>DNA</topic><topic>DNA, Viral - analysis</topic><topic>EIA</topic><topic>enzyme immunoassay</topic><topic>enzyme immunoassay-polymerase chain reaction</topic><topic>Enzymes</topic><topic>Genetic testing</topic><topic>HPV</topic><topic>Human papillomavirus</topic><topic>human papillomavirus antibody</topic><topic>Humans</topic><topic>Immunoassay</topic><topic>Immunohistochemistry - methods</topic><topic>Infections</topic><topic>Investigative techniques, diagnostic techniques (general aspects)</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Nephrology. Urinary tract diseases</topic><topic>Original</topic><topic>Papillomaviridae - immunology</topic><topic>Papillomaviridae - isolation &amp; purification</topic><topic>papillomavirus</topic><topic>Papillomavirus Infections - complications</topic><topic>Papillomavirus Infections - immunology</topic><topic>Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques</topic><topic>PCR</topic><topic>Plasmids</topic><topic>Polyclonal antibodies</topic><topic>Polymerase chain reaction</topic><topic>Polymerase Chain Reaction - methods</topic><topic>Studies</topic><topic>TCC</topic><topic>transitional cell carcinoma</topic><topic>Tumors</topic><topic>Tumors of the urinary system</topic><topic>Urinary Bladder Neoplasms - immunology</topic><topic>Urinary Bladder Neoplasms - virology</topic><topic>Urinary tract. Prostate gland</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Youshya, S</creatorcontrib><creatorcontrib>Purdie, K</creatorcontrib><creatorcontrib>Breuer, J</creatorcontrib><creatorcontrib>Proby, C</creatorcontrib><creatorcontrib>Sheaf, M T</creatorcontrib><creatorcontrib>Oliver, R T D</creatorcontrib><creatorcontrib>Baithun, S</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>ProQuest Central (Corporate)</collection><collection>Health &amp; 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 Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>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 &amp; Medical Complete (Alumni)</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database</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>MEDLINE - Academic</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>Youshya, S</au><au>Purdie, K</au><au>Breuer, J</au><au>Proby, C</au><au>Sheaf, M T</au><au>Oliver, R T D</au><au>Baithun, S</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Does human papillomavirus play a role in the development of bladder transitional cell carcinoma? 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The second method was a consensus GP5+/6+ primer mediated polymerase chain reaction (PCR) technique, with the products analysed by both agarose gel electrophoresis and an enzyme immunoassay using type specific oligonucleotide probes for 10 different mucosal genotypes. To exclude false negative results because of the poor quality of DNA extracted from paraffin wax embedded samples, the series was extended to include 20 further blocks for which the corresponding snap frozen unfixed tissue was available. Results: The two methods produced contrasting results, with 47 of the 78 samples positive for HPV antigen and none positive for HPV DNA. HPV DNA was not detected in the 20 additional paraffin wax embedded TCCs or in the 20 paired unfixed samples. In contrast, HPV DNA was amplified by PCR from all six of the paraffin wax embedded cervical carcinoma and anogenital wart control samples. Conclusion: The disparity between the two sets of results is probably caused by false positives resulting from the non-specificity of the polyclonal antibody used for immunohistochemistry. These results suggest that HPV is unlikely to play an aetiological role in the development of bladder TCC.</abstract><cop>London</cop><pub>BMJ Publishing Group Ltd and Association of Clinical Pathologists</pub><pmid>15677544</pmid><doi>10.1136/jcp.2004.017152</doi><tpages>4</tpages><oa>free_for_read</oa></addata></record>
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subjects Adult
Aged
Aged, 80 and over
Antibodies, Viral - analysis
Antibody Specificity - immunology
Antigens
Antigens, Viral - analysis
Biological and medical sciences
Biopsy
Bladder
bladder cancer
Capsid Proteins - analysis
Carcinoma, Transitional Cell - immunology
Carcinoma, Transitional Cell - virology
Cervical cancer
Deoxyribonucleic acid
DIG
digoxigenin
DNA
DNA, Viral - analysis
EIA
enzyme immunoassay
enzyme immunoassay-polymerase chain reaction
Enzymes
Genetic testing
HPV
Human papillomavirus
human papillomavirus antibody
Humans
Immunoassay
Immunohistochemistry - methods
Infections
Investigative techniques, diagnostic techniques (general aspects)
Medical sciences
Middle Aged
Nephrology. Urinary tract diseases
Original
Papillomaviridae - immunology
Papillomaviridae - isolation & purification
papillomavirus
Papillomavirus Infections - complications
Papillomavirus Infections - immunology
Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques
PCR
Plasmids
Polyclonal antibodies
Polymerase chain reaction
Polymerase Chain Reaction - methods
Studies
TCC
transitional cell carcinoma
Tumors
Tumors of the urinary system
Urinary Bladder Neoplasms - immunology
Urinary Bladder Neoplasms - virology
Urinary tract. Prostate gland
title Does human papillomavirus play a role in the development of bladder transitional cell carcinoma? A comparison of PCR and immunohistochemical analysis
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