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Immunohistochemistry and Fluorescence In Situ Hybridization Can Inform the Differential Diagnosis of Low-Grade Noninvasive Urothelial Carcinoma with an Inverted Growth Pattern and Inverted Urothelial Papilloma
Urothelial carcinoma (UC) comprises a heterogeneous group of epithelial neoplasms with diverse biological behaviors and variable clinical outcomes. Distinguishing UC histological subtypes has become increasingly important because prognoses and therapy can dramatically differ among subtypes. In clini...
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Published in: | PloS one 2015-07, Vol.10 (7), p.e0133530-e0133530 |
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description | Urothelial carcinoma (UC) comprises a heterogeneous group of epithelial neoplasms with diverse biological behaviors and variable clinical outcomes. Distinguishing UC histological subtypes has become increasingly important because prognoses and therapy can dramatically differ among subtypes. In clinical work, overlapping morphological findings between low-grade noninvasive UC (LGNUC), which exhibits an inverted growth pattern, and inverted urothelial papilloma (IUP) can make subclassification difficult. We propose a combination of immunohistochemistry (IHC) and molecular cytogenetics for subtyping these clinical entities. In our study, tissue microarray immunohistochemical profiles of Ki-67, p53, cytokeratin 20 (CK20) and cyclinD1 were assessed. Molecular genetic alterations such as the gain of chromosomes 3, 7 or 17 or the homozygous loss of 9p21 were also assessed for their usefulness in differentiating these conditions. Based on our analysis, Ki-67 and CK20 may be useful for the differential diagnosis of these two tumor types. Fluorescence in situ hybridization (FISH) can also provide important data in cases in which the malignant nature of an inverted urothelial neoplasm is unclear. LGNUC with an inverted growth pattern that is negative for both Ki-67 and CK20 can be positively detected using FISH. |
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Distinguishing UC histological subtypes has become increasingly important because prognoses and therapy can dramatically differ among subtypes. In clinical work, overlapping morphological findings between low-grade noninvasive UC (LGNUC), which exhibits an inverted growth pattern, and inverted urothelial papilloma (IUP) can make subclassification difficult. We propose a combination of immunohistochemistry (IHC) and molecular cytogenetics for subtyping these clinical entities. In our study, tissue microarray immunohistochemical profiles of Ki-67, p53, cytokeratin 20 (CK20) and cyclinD1 were assessed. Molecular genetic alterations such as the gain of chromosomes 3, 7 or 17 or the homozygous loss of 9p21 were also assessed for their usefulness in differentiating these conditions. Based on our analysis, Ki-67 and CK20 may be useful for the differential diagnosis of these two tumor types. Fluorescence in situ hybridization (FISH) can also provide important data in cases in which the malignant nature of an inverted urothelial neoplasm is unclear. LGNUC with an inverted growth pattern that is negative for both Ki-67 and CK20 can be positively detected using FISH.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0133530</identifier><identifier>PMID: 26208279</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Biomarkers, Tumor ; Bladder cancer ; Carcinoma ; Carcinoma - diagnosis ; Carcinoma - mortality ; Cell cycle ; Chromosomes ; Consent ; Cytogenetics ; Cytokeratin ; Diagnosis ; Diagnosis, Differential ; Differential diagnosis ; Ethics ; Fluorescence ; Fluorescence in situ hybridization ; Growth ; Humans ; Hybridization ; Immunohistochemistry ; In Situ Hybridization, Fluorescence ; Kaplan-Meier Estimate ; Labeling ; Medical diagnosis ; Medical research ; Neoplasia ; Neoplasm Grading ; Neoplasms ; Oncology ; p53 Protein ; Papilloma ; Papilloma, Inverted - diagnosis ; Pathology ; Prognosis ; Tumor proteins ; Tumors ; Urologic Neoplasms - diagnosis ; Urologic Neoplasms - mortality ; Urothelial carcinoma</subject><ispartof>PloS one, 2015-07, Vol.10 (7), p.e0133530-e0133530</ispartof><rights>COPYRIGHT 2015 Public Library of Science</rights><rights>2015 Sun et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2015 Sun et al 2015 Sun et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c692t-a24b359c178f2bda87e3dca1919d4a8f52903b5532afd992fc3648375332f4283</citedby><cites>FETCH-LOGICAL-c692t-a24b359c178f2bda87e3dca1919d4a8f52903b5532afd992fc3648375332f4283</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/1698611549/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1698611549?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25752,27923,27924,37011,37012,44589,53790,53792,74897</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26208279$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Real, Francisco X.</contributor><creatorcontrib>Sun, Juan-Juan</creatorcontrib><creatorcontrib>Wu, Yong</creatorcontrib><creatorcontrib>Lu, Yong-Ming</creatorcontrib><creatorcontrib>Zhang, Hui-Zhi</creatorcontrib><creatorcontrib>Wang, Tao</creatorcontrib><creatorcontrib>Yang, Xiao-Qun</creatorcontrib><creatorcontrib>Sun, Meng-Hong</creatorcontrib><creatorcontrib>Wang, Chao-Fu</creatorcontrib><title>Immunohistochemistry and Fluorescence In Situ Hybridization Can Inform the Differential Diagnosis of Low-Grade Noninvasive Urothelial Carcinoma with an Inverted Growth Pattern and Inverted Urothelial Papilloma</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>Urothelial carcinoma (UC) comprises a heterogeneous group of epithelial neoplasms with diverse biological behaviors and variable clinical outcomes. 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Fluorescence in situ hybridization (FISH) can also provide important data in cases in which the malignant nature of an inverted urothelial neoplasm is unclear. LGNUC with an inverted growth pattern that is negative for both Ki-67 and CK20 can be positively detected using FISH.</description><subject>Biomarkers, Tumor</subject><subject>Bladder cancer</subject><subject>Carcinoma</subject><subject>Carcinoma - diagnosis</subject><subject>Carcinoma - mortality</subject><subject>Cell cycle</subject><subject>Chromosomes</subject><subject>Consent</subject><subject>Cytogenetics</subject><subject>Cytokeratin</subject><subject>Diagnosis</subject><subject>Diagnosis, Differential</subject><subject>Differential diagnosis</subject><subject>Ethics</subject><subject>Fluorescence</subject><subject>Fluorescence in situ hybridization</subject><subject>Growth</subject><subject>Humans</subject><subject>Hybridization</subject><subject>Immunohistochemistry</subject><subject>In Situ Hybridization, Fluorescence</subject><subject>Kaplan-Meier Estimate</subject><subject>Labeling</subject><subject>Medical diagnosis</subject><subject>Medical research</subject><subject>Neoplasia</subject><subject>Neoplasm Grading</subject><subject>Neoplasms</subject><subject>Oncology</subject><subject>p53 Protein</subject><subject>Papilloma</subject><subject>Papilloma, Inverted - diagnosis</subject><subject>Pathology</subject><subject>Prognosis</subject><subject>Tumor proteins</subject><subject>Tumors</subject><subject>Urologic Neoplasms - diagnosis</subject><subject>Urologic Neoplasms - mortality</subject><subject>Urothelial carcinoma</subject><issn>1932-6203</issn><issn>1932-6203</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNqNk81uEzEQx1cIREvhDRBYQkJwSNi198sXpCrQNlJFK0q5WrP-yLpy7NT2ppS35I1w0rRKUA9oD16Pf_OfsWcmy14X-bggTfHpyg3eghkvnJXjvCCkIvmTbL-gBI9qnJOnW_972YsQrvK8Im1dP8_2cDK2uKH72Z_pfD5Y1-sQHe_lPK3-FoEV6MgMzsvApeUSTS260HFAJ7ed10L_hqidRROw6UQ5P0exl-iLVkp6aaMGkzYwsy7ogJxCp-5mdOxBSPTNWW2XEPRSokvvkptZ0RPwXFs3B3SjY4_WukvpoxTo2LubZDqHGKW369QezrYUzmGhjUkKL7NnCkyQrzbrQXZ59PXH5GR0enY8nRyejnhNcRwBLjtSUV40rcKdgLaRRHAoaEFFCa2qMM1JV1UEgxKUYsVJXbakqQjBqsQtOcje3ukujAtsU43Aipq2dVFUJU3E9I4QDq7Ywus5-FvmQLO1wfkZAx81N5J1tShJ3XYVdGXZ0bqtK6VSGJHXoqt4k7Q-b6IN3VyKVJXoweyI7p5Y3bOZW7KyKsp6ncyHjYB314MMkaVac2kMWOmGdd60pLhpcULf_YM-frsNNYN0AZ3aIMXlK1F2WGJMKW3T6x1k40eo9InUazy1rtLJvuPwccchMVH-ijMYQmDTi-__z5793GXfb7G9BBP74MywauSwC5Z3IPcuBC_VwyMXOVtN3v1rsNXksc3kJbc32wV6cLofNfIXIJstnA</recordid><startdate>20150724</startdate><enddate>20150724</enddate><creator>Sun, Juan-Juan</creator><creator>Wu, Yong</creator><creator>Lu, Yong-Ming</creator><creator>Zhang, Hui-Zhi</creator><creator>Wang, Tao</creator><creator>Yang, Xiao-Qun</creator><creator>Sun, Meng-Hong</creator><creator>Wang, Chao-Fu</creator><general>Public Library of Science</general><general>Public Library of Science (PLoS)</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>IOV</scope><scope>ISR</scope><scope>3V.</scope><scope>7QG</scope><scope>7QL</scope><scope>7QO</scope><scope>7RV</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TG</scope><scope>7TM</scope><scope>7U9</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB.</scope><scope>KB0</scope><scope>KL.</scope><scope>L6V</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>M7S</scope><scope>NAPCQ</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PATMY</scope><scope>PDBOC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PTHSS</scope><scope>PYCSY</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20150724</creationdate><title>Immunohistochemistry and Fluorescence In Situ Hybridization Can Inform the Differential Diagnosis of Low-Grade Noninvasive Urothelial Carcinoma with an Inverted Growth Pattern and Inverted Urothelial Papilloma</title><author>Sun, Juan-Juan ; Wu, Yong ; Lu, Yong-Ming ; Zhang, Hui-Zhi ; Wang, Tao ; Yang, Xiao-Qun ; Sun, Meng-Hong ; Wang, Chao-Fu</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c692t-a24b359c178f2bda87e3dca1919d4a8f52903b5532afd992fc3648375332f4283</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Biomarkers, Tumor</topic><topic>Bladder cancer</topic><topic>Carcinoma</topic><topic>Carcinoma - 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Distinguishing UC histological subtypes has become increasingly important because prognoses and therapy can dramatically differ among subtypes. In clinical work, overlapping morphological findings between low-grade noninvasive UC (LGNUC), which exhibits an inverted growth pattern, and inverted urothelial papilloma (IUP) can make subclassification difficult. We propose a combination of immunohistochemistry (IHC) and molecular cytogenetics for subtyping these clinical entities. In our study, tissue microarray immunohistochemical profiles of Ki-67, p53, cytokeratin 20 (CK20) and cyclinD1 were assessed. Molecular genetic alterations such as the gain of chromosomes 3, 7 or 17 or the homozygous loss of 9p21 were also assessed for their usefulness in differentiating these conditions. Based on our analysis, Ki-67 and CK20 may be useful for the differential diagnosis of these two tumor types. Fluorescence in situ hybridization (FISH) can also provide important data in cases in which the malignant nature of an inverted urothelial neoplasm is unclear. LGNUC with an inverted growth pattern that is negative for both Ki-67 and CK20 can be positively detected using FISH.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>26208279</pmid><doi>10.1371/journal.pone.0133530</doi><oa>free_for_read</oa></addata></record> |
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subjects | Biomarkers, Tumor Bladder cancer Carcinoma Carcinoma - diagnosis Carcinoma - mortality Cell cycle Chromosomes Consent Cytogenetics Cytokeratin Diagnosis Diagnosis, Differential Differential diagnosis Ethics Fluorescence Fluorescence in situ hybridization Growth Humans Hybridization Immunohistochemistry In Situ Hybridization, Fluorescence Kaplan-Meier Estimate Labeling Medical diagnosis Medical research Neoplasia Neoplasm Grading Neoplasms Oncology p53 Protein Papilloma Papilloma, Inverted - diagnosis Pathology Prognosis Tumor proteins Tumors Urologic Neoplasms - diagnosis Urologic Neoplasms - mortality Urothelial carcinoma |
title | Immunohistochemistry and Fluorescence In Situ Hybridization Can Inform the Differential Diagnosis of Low-Grade Noninvasive Urothelial Carcinoma with an Inverted Growth Pattern and Inverted Urothelial Papilloma |
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