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Prognostic value of TIGAR and LC3B protein expression in nasopharyngeal carcinoma
PURPOSE: Autophagy, the process responsible for degrading cytoplasmic organelles to sustain cellular metabolism, has been associated with cancer initiation and progression. As TP53-induced glycolysis and apoptosis regulator (TIGAR) is among the important genes that can regulate autophagy, we aimed t...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6237137/ https://www.ncbi.nlm.nih.gov/pubmed/30519107 http://dx.doi.org/10.2147/CMAR.S175501 |
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author | Wei, Min Peng, Jinxia Wu, Peng Chen, Ping Yang, Hongru Cui, Yongxia Yang, Linglin |
author_facet | Wei, Min Peng, Jinxia Wu, Peng Chen, Ping Yang, Hongru Cui, Yongxia Yang, Linglin |
author_sort | Wei, Min |
collection | PubMed |
description | PURPOSE: Autophagy, the process responsible for degrading cytoplasmic organelles to sustain cellular metabolism, has been associated with cancer initiation and progression. As TP53-induced glycolysis and apoptosis regulator (TIGAR) is among the important genes that can regulate autophagy, we aimed to investigate the correlation between the expression levels of TIGAR and the autophagy-related protein microtubule-associated protein 1 light chain 3 (LC3B), as well as their association with clinical outcomes, in nasopharyngeal carcinoma (NPC) patients. METHODS: We detected the expressions of TIGAR and LC3B in 182 NPC tissue samples via immunohistochemical staining. RESULTS: A significant correlation between TIGAR and LC3B expressions was identified (P=0.045). Moreover, survival analysis showed that TIGAR− or LC3B+ expression was associated with improved overall survival, local regional failure-free survival, distant failure-free survival, and failure-free survival rates, compared with TIGAR+ or LC3B− expression, respectively. Meanwhile, when combining TIGAR with LC3B expression in terms of prognostic value, patients with TIGAR+/LC3B− expression were significantly disadvantaged with regard to overall survival, local regional failure-free survival, distant failure-free survival, and failure-free survival compared with other groups based on the log-rank test and Cox regression analyses (all P<0.05). CONCLUSION: TIGAR and LC3B may be novel biomarkers for predicting the prognosis of NPC patients and could be utilized as potential targets for future therapeutics aimed at treating NPC patients. |
format | Online Article Text |
id | pubmed-6237137 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-62371372018-12-05 Prognostic value of TIGAR and LC3B protein expression in nasopharyngeal carcinoma Wei, Min Peng, Jinxia Wu, Peng Chen, Ping Yang, Hongru Cui, Yongxia Yang, Linglin Cancer Manag Res Original Research PURPOSE: Autophagy, the process responsible for degrading cytoplasmic organelles to sustain cellular metabolism, has been associated with cancer initiation and progression. As TP53-induced glycolysis and apoptosis regulator (TIGAR) is among the important genes that can regulate autophagy, we aimed to investigate the correlation between the expression levels of TIGAR and the autophagy-related protein microtubule-associated protein 1 light chain 3 (LC3B), as well as their association with clinical outcomes, in nasopharyngeal carcinoma (NPC) patients. METHODS: We detected the expressions of TIGAR and LC3B in 182 NPC tissue samples via immunohistochemical staining. RESULTS: A significant correlation between TIGAR and LC3B expressions was identified (P=0.045). Moreover, survival analysis showed that TIGAR− or LC3B+ expression was associated with improved overall survival, local regional failure-free survival, distant failure-free survival, and failure-free survival rates, compared with TIGAR+ or LC3B− expression, respectively. Meanwhile, when combining TIGAR with LC3B expression in terms of prognostic value, patients with TIGAR+/LC3B− expression were significantly disadvantaged with regard to overall survival, local regional failure-free survival, distant failure-free survival, and failure-free survival compared with other groups based on the log-rank test and Cox regression analyses (all P<0.05). CONCLUSION: TIGAR and LC3B may be novel biomarkers for predicting the prognosis of NPC patients and could be utilized as potential targets for future therapeutics aimed at treating NPC patients. Dove Medical Press 2018-11-12 /pmc/articles/PMC6237137/ /pubmed/30519107 http://dx.doi.org/10.2147/CMAR.S175501 Text en © 2018 Wei et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Wei, Min Peng, Jinxia Wu, Peng Chen, Ping Yang, Hongru Cui, Yongxia Yang, Linglin Prognostic value of TIGAR and LC3B protein expression in nasopharyngeal carcinoma |
title | Prognostic value of TIGAR and LC3B protein expression in nasopharyngeal carcinoma |
title_full | Prognostic value of TIGAR and LC3B protein expression in nasopharyngeal carcinoma |
title_fullStr | Prognostic value of TIGAR and LC3B protein expression in nasopharyngeal carcinoma |
title_full_unstemmed | Prognostic value of TIGAR and LC3B protein expression in nasopharyngeal carcinoma |
title_short | Prognostic value of TIGAR and LC3B protein expression in nasopharyngeal carcinoma |
title_sort | prognostic value of tigar and lc3b protein expression in nasopharyngeal carcinoma |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6237137/ https://www.ncbi.nlm.nih.gov/pubmed/30519107 http://dx.doi.org/10.2147/CMAR.S175501 |
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