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The Clinical Implications of Death Domain-Associated Protein (DAXX) Expression

BACKGROUND: Death domain-associated protein (DAXX), originally identified as a pro-apoptotic protein, is now understood to be either a pro-apoptotic or an anti-apoptotic factor with a chromatin remodeler, depending on the cell type and context. This study evaluated DAXX expression and its clinical i...

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Autores principales: Ko, Taek Yong, Kim, Jong In, Park, Eok Sung, Mun, Jeong Min, Park, Sung Dal
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society for Thoracic and Cardiovascular Surgery 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5973215/
https://www.ncbi.nlm.nih.gov/pubmed/29854663
http://dx.doi.org/10.5090/kjtcs.2018.51.3.187
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author Ko, Taek Yong
Kim, Jong In
Park, Eok Sung
Mun, Jeong Min
Park, Sung Dal
author_facet Ko, Taek Yong
Kim, Jong In
Park, Eok Sung
Mun, Jeong Min
Park, Sung Dal
author_sort Ko, Taek Yong
collection PubMed
description BACKGROUND: Death domain-associated protein (DAXX), originally identified as a pro-apoptotic protein, is now understood to be either a pro-apoptotic or an anti-apoptotic factor with a chromatin remodeler, depending on the cell type and context. This study evaluated DAXX expression and its clinical implications in squamous cell carcinoma of the esophagus. METHODS: Paraffin-embedded tissues from 60 cases of esophageal squamous carcinoma were analyzed immunohistochemically. An immune reaction with more than 10% of tumor cells was interpreted as positive. Positive reactions were sorted into 2 groups: reactions in 11%–50% of tumor cells and reactions in more than 51% of tumor cells, and the correlations between expression and survival and clinical prognosticators were analyzed. RESULTS: Forty-three of the 60 cases (71.7%) showed strong nuclear DAXX expression, among which 19 cases showed a positive reaction (31.7%) in 11%–50% of tumor cells, and 24 cases (40.0%) showed a positive reaction in more than 51% of tumor cells. A negative reaction was found in 17 cases (28.3%). These patterns of immunostaining were significantly associated with the N stage (p=0.005) and American Joint Committee on Cancer stage (p=0.001), but overall survival showed no significant difference. There were no correlations of DAXX expression with age, gender, or T stage. However, in stage IIB (p=0.046) and stage IV (p=0.014) disease, DAXX expression was significantly correlated with survival. CONCLUSION: This investigation found upregulation of DAXX in esophageal cancer, with a 71.7% expression rate. DAXX immunostaining could be used in clinical practice to predict aggressive tumors with lymph node metastasis in advanced-stage disease, especially in stages IIB and IV.
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spelling pubmed-59732152018-06-01 The Clinical Implications of Death Domain-Associated Protein (DAXX) Expression Ko, Taek Yong Kim, Jong In Park, Eok Sung Mun, Jeong Min Park, Sung Dal Korean J Thorac Cardiovasc Surg Clinical Research BACKGROUND: Death domain-associated protein (DAXX), originally identified as a pro-apoptotic protein, is now understood to be either a pro-apoptotic or an anti-apoptotic factor with a chromatin remodeler, depending on the cell type and context. This study evaluated DAXX expression and its clinical implications in squamous cell carcinoma of the esophagus. METHODS: Paraffin-embedded tissues from 60 cases of esophageal squamous carcinoma were analyzed immunohistochemically. An immune reaction with more than 10% of tumor cells was interpreted as positive. Positive reactions were sorted into 2 groups: reactions in 11%–50% of tumor cells and reactions in more than 51% of tumor cells, and the correlations between expression and survival and clinical prognosticators were analyzed. RESULTS: Forty-three of the 60 cases (71.7%) showed strong nuclear DAXX expression, among which 19 cases showed a positive reaction (31.7%) in 11%–50% of tumor cells, and 24 cases (40.0%) showed a positive reaction in more than 51% of tumor cells. A negative reaction was found in 17 cases (28.3%). These patterns of immunostaining were significantly associated with the N stage (p=0.005) and American Joint Committee on Cancer stage (p=0.001), but overall survival showed no significant difference. There were no correlations of DAXX expression with age, gender, or T stage. However, in stage IIB (p=0.046) and stage IV (p=0.014) disease, DAXX expression was significantly correlated with survival. CONCLUSION: This investigation found upregulation of DAXX in esophageal cancer, with a 71.7% expression rate. DAXX immunostaining could be used in clinical practice to predict aggressive tumors with lymph node metastasis in advanced-stage disease, especially in stages IIB and IV. The Korean Society for Thoracic and Cardiovascular Surgery 2018-06 2018-06-05 /pmc/articles/PMC5973215/ /pubmed/29854663 http://dx.doi.org/10.5090/kjtcs.2018.51.3.187 Text en Copyright © 2018 by The Korean Society for Thoracic and Cardiovascular Surgery. All rights Reserved. This is an open access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Research
Ko, Taek Yong
Kim, Jong In
Park, Eok Sung
Mun, Jeong Min
Park, Sung Dal
The Clinical Implications of Death Domain-Associated Protein (DAXX) Expression
title The Clinical Implications of Death Domain-Associated Protein (DAXX) Expression
title_full The Clinical Implications of Death Domain-Associated Protein (DAXX) Expression
title_fullStr The Clinical Implications of Death Domain-Associated Protein (DAXX) Expression
title_full_unstemmed The Clinical Implications of Death Domain-Associated Protein (DAXX) Expression
title_short The Clinical Implications of Death Domain-Associated Protein (DAXX) Expression
title_sort clinical implications of death domain-associated protein (daxx) expression
topic Clinical Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5973215/
https://www.ncbi.nlm.nih.gov/pubmed/29854663
http://dx.doi.org/10.5090/kjtcs.2018.51.3.187
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