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Downregulation of S100 Calcium Binding Protein A9 in Esophageal Squamous Cell Carcinoma

The development of esophageal squamous cell carcinoma (ESCC) is poorly understood and the major regulatory molecules involved in the process of tumorigenesis have not yet been identified. We had previously employed a quantitative proteomic approach to identify differentially expressed proteins in ES...

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Autores principales: Pawar, Harsh, Srikanth, Srinivas M., Kashyap, Manoj Kumar, Sathe, Gajanan, Chavan, Sandip, Singal, Mukul, Manju, H. C., Kumar, Kariyanakatte Veeraiah Veerendra, Vijayakumar, M., Sirdeshmukh, Ravi, Pandey, Akhilesh, Prasad, T. S. Keshava, Gowda, Harsha, Kumar, Rekha V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4691646/
https://www.ncbi.nlm.nih.gov/pubmed/26788548
http://dx.doi.org/10.1155/2015/325721
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author Pawar, Harsh
Srikanth, Srinivas M.
Kashyap, Manoj Kumar
Sathe, Gajanan
Chavan, Sandip
Singal, Mukul
Manju, H. C.
Kumar, Kariyanakatte Veeraiah Veerendra
Vijayakumar, M.
Sirdeshmukh, Ravi
Pandey, Akhilesh
Prasad, T. S. Keshava
Gowda, Harsha
Kumar, Rekha V.
author_facet Pawar, Harsh
Srikanth, Srinivas M.
Kashyap, Manoj Kumar
Sathe, Gajanan
Chavan, Sandip
Singal, Mukul
Manju, H. C.
Kumar, Kariyanakatte Veeraiah Veerendra
Vijayakumar, M.
Sirdeshmukh, Ravi
Pandey, Akhilesh
Prasad, T. S. Keshava
Gowda, Harsha
Kumar, Rekha V.
author_sort Pawar, Harsh
collection PubMed
description The development of esophageal squamous cell carcinoma (ESCC) is poorly understood and the major regulatory molecules involved in the process of tumorigenesis have not yet been identified. We had previously employed a quantitative proteomic approach to identify differentially expressed proteins in ESCC tumors. A total of 238 differentially expressed proteins were identified in that study including S100 calcium binding protein A9 (S100A9) as one of the major downregulated proteins. In the present study, we carried out immunohistochemical validation of S100A9 in a large cohort of ESCC patients to determine the expression and subcellular localization of S100A9 in tumors and adjacent normal esophageal epithelia. Downregulation of S100A9 was observed in 67% (n = 192) of 288 different ESCC tumors, with the most dramatic downregulation observed in the poorly differentiated tumors (99/111). Expression of S100A9 was restricted to the prickle and functional layers of normal esophageal mucosa and localized predominantly in the cytoplasm and nucleus whereas virtually no expression was observed in the tumor and stromal cells. This suggests the important role that S100A9 plays in maintaining the differentiated state of epithelium and suggests that its downregulation may be associated with increased susceptibility to tumor formation.
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spelling pubmed-46916462016-01-19 Downregulation of S100 Calcium Binding Protein A9 in Esophageal Squamous Cell Carcinoma Pawar, Harsh Srikanth, Srinivas M. Kashyap, Manoj Kumar Sathe, Gajanan Chavan, Sandip Singal, Mukul Manju, H. C. Kumar, Kariyanakatte Veeraiah Veerendra Vijayakumar, M. Sirdeshmukh, Ravi Pandey, Akhilesh Prasad, T. S. Keshava Gowda, Harsha Kumar, Rekha V. ScientificWorldJournal Research Article The development of esophageal squamous cell carcinoma (ESCC) is poorly understood and the major regulatory molecules involved in the process of tumorigenesis have not yet been identified. We had previously employed a quantitative proteomic approach to identify differentially expressed proteins in ESCC tumors. A total of 238 differentially expressed proteins were identified in that study including S100 calcium binding protein A9 (S100A9) as one of the major downregulated proteins. In the present study, we carried out immunohistochemical validation of S100A9 in a large cohort of ESCC patients to determine the expression and subcellular localization of S100A9 in tumors and adjacent normal esophageal epithelia. Downregulation of S100A9 was observed in 67% (n = 192) of 288 different ESCC tumors, with the most dramatic downregulation observed in the poorly differentiated tumors (99/111). Expression of S100A9 was restricted to the prickle and functional layers of normal esophageal mucosa and localized predominantly in the cytoplasm and nucleus whereas virtually no expression was observed in the tumor and stromal cells. This suggests the important role that S100A9 plays in maintaining the differentiated state of epithelium and suggests that its downregulation may be associated with increased susceptibility to tumor formation. Hindawi Publishing Corporation 2015 2015-12-14 /pmc/articles/PMC4691646/ /pubmed/26788548 http://dx.doi.org/10.1155/2015/325721 Text en Copyright © 2015 Harsh Pawar et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Pawar, Harsh
Srikanth, Srinivas M.
Kashyap, Manoj Kumar
Sathe, Gajanan
Chavan, Sandip
Singal, Mukul
Manju, H. C.
Kumar, Kariyanakatte Veeraiah Veerendra
Vijayakumar, M.
Sirdeshmukh, Ravi
Pandey, Akhilesh
Prasad, T. S. Keshava
Gowda, Harsha
Kumar, Rekha V.
Downregulation of S100 Calcium Binding Protein A9 in Esophageal Squamous Cell Carcinoma
title Downregulation of S100 Calcium Binding Protein A9 in Esophageal Squamous Cell Carcinoma
title_full Downregulation of S100 Calcium Binding Protein A9 in Esophageal Squamous Cell Carcinoma
title_fullStr Downregulation of S100 Calcium Binding Protein A9 in Esophageal Squamous Cell Carcinoma
title_full_unstemmed Downregulation of S100 Calcium Binding Protein A9 in Esophageal Squamous Cell Carcinoma
title_short Downregulation of S100 Calcium Binding Protein A9 in Esophageal Squamous Cell Carcinoma
title_sort downregulation of s100 calcium binding protein a9 in esophageal squamous cell carcinoma
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4691646/
https://www.ncbi.nlm.nih.gov/pubmed/26788548
http://dx.doi.org/10.1155/2015/325721
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