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E-cadherin and Cytokeratin Subtype Profiling in Effusion Cytology

Diagnostic utility of E-cadherin (E-CD) and cytokeratin (CK) subtype profiling in effusion cytology was investigated, employing immunocytochemistry on cellblock sections available from 211 metastatic carcinomas (MC), 6 mesotheliomas and 73 reactive mesothelial hyperplasias (MH). E-CD and monoclonal...

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Autores principales: Han, Joungho, Kim, Mi-Kyung, Nam, Seok-Jin, Yang, Jung-Hyun
Formato: Texto
Lenguaje:English
Publicado: The Korean Academy of Medical Sciences 2004
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2816286/
https://www.ncbi.nlm.nih.gov/pubmed/15608393
http://dx.doi.org/10.3346/jkms.2004.19.6.826
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author Han, Joungho
Kim, Mi-Kyung
Nam, Seok-Jin
Yang, Jung-Hyun
author_facet Han, Joungho
Kim, Mi-Kyung
Nam, Seok-Jin
Yang, Jung-Hyun
author_sort Han, Joungho
collection PubMed
description Diagnostic utility of E-cadherin (E-CD) and cytokeratin (CK) subtype profiling in effusion cytology was investigated, employing immunocytochemistry on cellblock sections available from 211 metastatic carcinomas (MC), 6 mesotheliomas and 73 reactive mesothelial hyperplasias (MH). E-CD and monoclonal carcinoembryonic anti-gen (mCEA) stained 85% (120/141) and 65% (138/211) of MC, respectively. E-CD staining of MC was frequently heterogeneous (76/120) and absent in all anaplastic carcinomas (0/2). E-CD stained none (0/57) of MH while mCEA and epithelial membrane antigen (EMA) stained 12% (9/73) and 32% (16/32) of MH, respectively. Of 6 mesotheliomas, E-CD focally stained in 2 while mCEA stained none and EMA stained all. CK20 and CK17 stained none of MH or mesotheliomas. CK20 stained 15% of MC and CK 17 stained 22% of MC. CK5/6 and high molecular weight CK stained all mesotheliomas, 56% and 88% of MH, 26% and 39% of MC, respectively. MC showed predominant CK7+/20- expression, with the exceptions of MC from mucinous type of colon/rectum and ovary showing predominant CK20 positive. E-CD may be a useful positive marker for MC in effusion cytology, although it may focally stain in some mesotheliomas. Any positive staining for CK20 of MC suggests MC from the gastrointestinal tract or ovary among others.
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spelling pubmed-28162862010-02-04 E-cadherin and Cytokeratin Subtype Profiling in Effusion Cytology Han, Joungho Kim, Mi-Kyung Nam, Seok-Jin Yang, Jung-Hyun J Korean Med Sci Original Article Diagnostic utility of E-cadherin (E-CD) and cytokeratin (CK) subtype profiling in effusion cytology was investigated, employing immunocytochemistry on cellblock sections available from 211 metastatic carcinomas (MC), 6 mesotheliomas and 73 reactive mesothelial hyperplasias (MH). E-CD and monoclonal carcinoembryonic anti-gen (mCEA) stained 85% (120/141) and 65% (138/211) of MC, respectively. E-CD staining of MC was frequently heterogeneous (76/120) and absent in all anaplastic carcinomas (0/2). E-CD stained none (0/57) of MH while mCEA and epithelial membrane antigen (EMA) stained 12% (9/73) and 32% (16/32) of MH, respectively. Of 6 mesotheliomas, E-CD focally stained in 2 while mCEA stained none and EMA stained all. CK20 and CK17 stained none of MH or mesotheliomas. CK20 stained 15% of MC and CK 17 stained 22% of MC. CK5/6 and high molecular weight CK stained all mesotheliomas, 56% and 88% of MH, 26% and 39% of MC, respectively. MC showed predominant CK7+/20- expression, with the exceptions of MC from mucinous type of colon/rectum and ovary showing predominant CK20 positive. E-CD may be a useful positive marker for MC in effusion cytology, although it may focally stain in some mesotheliomas. Any positive staining for CK20 of MC suggests MC from the gastrointestinal tract or ovary among others. The Korean Academy of Medical Sciences 2004-12 2004-12-31 /pmc/articles/PMC2816286/ /pubmed/15608393 http://dx.doi.org/10.3346/jkms.2004.19.6.826 Text en Copyright © 2004 The Korean Academy of Medical Sciences http://creativecommons.org/licenses/by-nc/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Han, Joungho
Kim, Mi-Kyung
Nam, Seok-Jin
Yang, Jung-Hyun
E-cadherin and Cytokeratin Subtype Profiling in Effusion Cytology
title E-cadherin and Cytokeratin Subtype Profiling in Effusion Cytology
title_full E-cadherin and Cytokeratin Subtype Profiling in Effusion Cytology
title_fullStr E-cadherin and Cytokeratin Subtype Profiling in Effusion Cytology
title_full_unstemmed E-cadherin and Cytokeratin Subtype Profiling in Effusion Cytology
title_short E-cadherin and Cytokeratin Subtype Profiling in Effusion Cytology
title_sort e-cadherin and cytokeratin subtype profiling in effusion cytology
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2816286/
https://www.ncbi.nlm.nih.gov/pubmed/15608393
http://dx.doi.org/10.3346/jkms.2004.19.6.826
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