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Cell Surface Human Airway Trypsin‐Like Protease Is Lost During Squamous Cell Carcinogenesis

Cancer progression is accompanied by increased levels of extracellular proteases that are capable of remodeling the extracellular matrix, as well as cleaving and activating growth factors and receptors that are involved in pro‐cancerous signaling pathways. Several members of the type II transmembran...

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Autores principales: Duhaime, Michael J., Page, Khaliph O., Varela, Fausto A., Murray, Andrew S., Silverman, Michael E., Zoratti, Gina L., List, Karin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4933652/
https://www.ncbi.nlm.nih.gov/pubmed/26297835
http://dx.doi.org/10.1002/jcp.25173
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author Duhaime, Michael J.
Page, Khaliph O.
Varela, Fausto A.
Murray, Andrew S.
Silverman, Michael E.
Zoratti, Gina L.
List, Karin
author_facet Duhaime, Michael J.
Page, Khaliph O.
Varela, Fausto A.
Murray, Andrew S.
Silverman, Michael E.
Zoratti, Gina L.
List, Karin
author_sort Duhaime, Michael J.
collection PubMed
description Cancer progression is accompanied by increased levels of extracellular proteases that are capable of remodeling the extracellular matrix, as well as cleaving and activating growth factors and receptors that are involved in pro‐cancerous signaling pathways. Several members of the type II transmembrane serine protease (TTSP) family have been shown to play critical roles in cancer progression, however, the expression or function of the TTSP Human Airway Trypsin‐like protease (HAT) in carcinogenesis has not been examined. In the present study we aimed to determine the expression of HAT during squamous cell carcinogenesis. HAT transcript is present in several tissues containing stratified squamous epithelium and decreased expression is observed in carcinomas. We determined that HAT protein is consistently expressed on the cell surface in suprabasal/apical layers of squamous cells in healthy cervical and esophageal epithelia. To assess whether HAT protein is differentially expressed in normal tissue versus tissue in different stages of carcinogenesis, we performed a comprehensive immunohistochemical analysis of HAT protein expression levels and localization in arrays of paraffin embedded human cervical and esophageal carcinomas compared to the corresponding normal tissue. We found that HAT protein is expressed in the non‐proliferating, differentiated cellular strata and is lost during the dedifferentiation of epithelial cells, a hallmark of squamous cell carcinogenesis. Thus, HAT expression may potentially be useful as a marker for clinical grading and assessment of patient prognosis in squamous cell carcinomas. J. Cell. Physiol. 231: 1476–1483, 2016. © 2015 Wiley Periodicals, Inc.
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spelling pubmed-49336522016-07-05 Cell Surface Human Airway Trypsin‐Like Protease Is Lost During Squamous Cell Carcinogenesis Duhaime, Michael J. Page, Khaliph O. Varela, Fausto A. Murray, Andrew S. Silverman, Michael E. Zoratti, Gina L. List, Karin J Cell Physiol Original Research Articles Cancer progression is accompanied by increased levels of extracellular proteases that are capable of remodeling the extracellular matrix, as well as cleaving and activating growth factors and receptors that are involved in pro‐cancerous signaling pathways. Several members of the type II transmembrane serine protease (TTSP) family have been shown to play critical roles in cancer progression, however, the expression or function of the TTSP Human Airway Trypsin‐like protease (HAT) in carcinogenesis has not been examined. In the present study we aimed to determine the expression of HAT during squamous cell carcinogenesis. HAT transcript is present in several tissues containing stratified squamous epithelium and decreased expression is observed in carcinomas. We determined that HAT protein is consistently expressed on the cell surface in suprabasal/apical layers of squamous cells in healthy cervical and esophageal epithelia. To assess whether HAT protein is differentially expressed in normal tissue versus tissue in different stages of carcinogenesis, we performed a comprehensive immunohistochemical analysis of HAT protein expression levels and localization in arrays of paraffin embedded human cervical and esophageal carcinomas compared to the corresponding normal tissue. We found that HAT protein is expressed in the non‐proliferating, differentiated cellular strata and is lost during the dedifferentiation of epithelial cells, a hallmark of squamous cell carcinogenesis. Thus, HAT expression may potentially be useful as a marker for clinical grading and assessment of patient prognosis in squamous cell carcinomas. J. Cell. Physiol. 231: 1476–1483, 2016. © 2015 Wiley Periodicals, Inc. John Wiley and Sons Inc. 2016-02-04 2016-07 /pmc/articles/PMC4933652/ /pubmed/26297835 http://dx.doi.org/10.1002/jcp.25173 Text en © 2015 Wiley Periodicals, Inc. This article is being made freely available through PubMed Central as part of the COVID-19 public health emergency response. It can be used for unrestricted research re-use and analysis in any form or by any means with acknowledgement of the original source, for the duration of the public health emergency.
spellingShingle Original Research Articles
Duhaime, Michael J.
Page, Khaliph O.
Varela, Fausto A.
Murray, Andrew S.
Silverman, Michael E.
Zoratti, Gina L.
List, Karin
Cell Surface Human Airway Trypsin‐Like Protease Is Lost During Squamous Cell Carcinogenesis
title Cell Surface Human Airway Trypsin‐Like Protease Is Lost During Squamous Cell Carcinogenesis
title_full Cell Surface Human Airway Trypsin‐Like Protease Is Lost During Squamous Cell Carcinogenesis
title_fullStr Cell Surface Human Airway Trypsin‐Like Protease Is Lost During Squamous Cell Carcinogenesis
title_full_unstemmed Cell Surface Human Airway Trypsin‐Like Protease Is Lost During Squamous Cell Carcinogenesis
title_short Cell Surface Human Airway Trypsin‐Like Protease Is Lost During Squamous Cell Carcinogenesis
title_sort cell surface human airway trypsin‐like protease is lost during squamous cell carcinogenesis
topic Original Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4933652/
https://www.ncbi.nlm.nih.gov/pubmed/26297835
http://dx.doi.org/10.1002/jcp.25173
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