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CDKN3 expression is an independent prognostic factor and associated with advanced tumor stage in nasopharyngeal carcinoma
Background: Through data mining from the public transcriptome of NPC, cyclin-dependent kinase inhibitor 3 (CDKN3) was identified as a significantly upregulated gene in NPC. CDKN3 functions as a key factor in cell cycle regulation. This study was aimed to investigate the expression of CDKN3 in NPC ti...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Ivyspring International Publisher
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6036165/ https://www.ncbi.nlm.nih.gov/pubmed/30013440 http://dx.doi.org/10.7150/ijms.25065 |
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author | Chang, Shih-Lun Chen, Tzu-Ju Lee, Ying-En Lee, Sung-Wei Lin, Li-Ching He, Hong-Lin |
author_facet | Chang, Shih-Lun Chen, Tzu-Ju Lee, Ying-En Lee, Sung-Wei Lin, Li-Ching He, Hong-Lin |
author_sort | Chang, Shih-Lun |
collection | PubMed |
description | Background: Through data mining from the public transcriptome of NPC, cyclin-dependent kinase inhibitor 3 (CDKN3) was identified as a significantly upregulated gene in NPC. CDKN3 functions as a key factor in cell cycle regulation. This study was aimed to investigate the expression of CDKN3 in NPC tissues and its prognostic significance. Methods: Immunohistochemistry was performed for 124 NPC patients to assess the protein expression of CDKN3. The stainings of CDKN3 were scored by using H-score method. The relationships between CDKN3 expression status and clinicopathological parameters, disease-specific survival (DSS), distant metastasis-free survival (DMeFS), and local recurrence-free survival (LRFS) were statistically analyzed. Results: High expression of CDKN3 was significantly associated with higher primary nodal status (P=0.030) and higher TNM stage (P=0.019). In univariate analysis, high expression of CDKN3 predicted worse DSS (P<0.0001), DMeFS (P<0.0001), and LRFS (P<0.0001). In multivariate analysis, CDKN3 overexpression still acted as an independent prognostic factor for worse DSS (P<0.001; hazard ratio [HR]=11.999, 95% CI: 5.378-26.771), DMeFS (P<0.001; HR=15.069, 95% CI: 5.884-38.592), and LRFS (P<0.001; HR=5.000, 95% CI: 2.312-10.815). Conclusion: High expression of CDKN3 was an independent negative prognostic factor for NPC and was associated with advanced disease status. It might serve as potential therapeutic target and aid in risk stratification for patients with NPC. |
format | Online Article Text |
id | pubmed-6036165 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Ivyspring International Publisher |
record_format | MEDLINE/PubMed |
spelling | pubmed-60361652018-07-16 CDKN3 expression is an independent prognostic factor and associated with advanced tumor stage in nasopharyngeal carcinoma Chang, Shih-Lun Chen, Tzu-Ju Lee, Ying-En Lee, Sung-Wei Lin, Li-Ching He, Hong-Lin Int J Med Sci Research Paper Background: Through data mining from the public transcriptome of NPC, cyclin-dependent kinase inhibitor 3 (CDKN3) was identified as a significantly upregulated gene in NPC. CDKN3 functions as a key factor in cell cycle regulation. This study was aimed to investigate the expression of CDKN3 in NPC tissues and its prognostic significance. Methods: Immunohistochemistry was performed for 124 NPC patients to assess the protein expression of CDKN3. The stainings of CDKN3 were scored by using H-score method. The relationships between CDKN3 expression status and clinicopathological parameters, disease-specific survival (DSS), distant metastasis-free survival (DMeFS), and local recurrence-free survival (LRFS) were statistically analyzed. Results: High expression of CDKN3 was significantly associated with higher primary nodal status (P=0.030) and higher TNM stage (P=0.019). In univariate analysis, high expression of CDKN3 predicted worse DSS (P<0.0001), DMeFS (P<0.0001), and LRFS (P<0.0001). In multivariate analysis, CDKN3 overexpression still acted as an independent prognostic factor for worse DSS (P<0.001; hazard ratio [HR]=11.999, 95% CI: 5.378-26.771), DMeFS (P<0.001; HR=15.069, 95% CI: 5.884-38.592), and LRFS (P<0.001; HR=5.000, 95% CI: 2.312-10.815). Conclusion: High expression of CDKN3 was an independent negative prognostic factor for NPC and was associated with advanced disease status. It might serve as potential therapeutic target and aid in risk stratification for patients with NPC. Ivyspring International Publisher 2018-06-14 /pmc/articles/PMC6036165/ /pubmed/30013440 http://dx.doi.org/10.7150/ijms.25065 Text en © Ivyspring International Publisher This is an open access article distributed under the terms of the Creative Commons Attribution (CC BY-NC) license (https://creativecommons.org/licenses/by-nc/4.0/). See http://ivyspring.com/terms for full terms and conditions. |
spellingShingle | Research Paper Chang, Shih-Lun Chen, Tzu-Ju Lee, Ying-En Lee, Sung-Wei Lin, Li-Ching He, Hong-Lin CDKN3 expression is an independent prognostic factor and associated with advanced tumor stage in nasopharyngeal carcinoma |
title | CDKN3 expression is an independent prognostic factor and associated with advanced tumor stage in nasopharyngeal carcinoma |
title_full | CDKN3 expression is an independent prognostic factor and associated with advanced tumor stage in nasopharyngeal carcinoma |
title_fullStr | CDKN3 expression is an independent prognostic factor and associated with advanced tumor stage in nasopharyngeal carcinoma |
title_full_unstemmed | CDKN3 expression is an independent prognostic factor and associated with advanced tumor stage in nasopharyngeal carcinoma |
title_short | CDKN3 expression is an independent prognostic factor and associated with advanced tumor stage in nasopharyngeal carcinoma |
title_sort | cdkn3 expression is an independent prognostic factor and associated with advanced tumor stage in nasopharyngeal carcinoma |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6036165/ https://www.ncbi.nlm.nih.gov/pubmed/30013440 http://dx.doi.org/10.7150/ijms.25065 |
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