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Dectin-1 predicts adverse postoperative prognosis of patients with clear cell renal cell carcinoma
Dectin-1, a classical pattern-recognition receptor, was now identified as an important regulator in immune homeostasis and cancer immunity through its extensive ligands binding functions and subsequent cytokines production. The aim of this study was to assess the clinical significance of dectin-1 ex...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5013447/ https://www.ncbi.nlm.nih.gov/pubmed/27600310 http://dx.doi.org/10.1038/srep32657 |
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author | Xia, Yu Liu, Li Bai, Qi Wang, Jiajun Xi, Wei Qu, Yang Xiong, Ying Long, Qilai Xu, Jiejie Guo, Jianming |
author_facet | Xia, Yu Liu, Li Bai, Qi Wang, Jiajun Xi, Wei Qu, Yang Xiong, Ying Long, Qilai Xu, Jiejie Guo, Jianming |
author_sort | Xia, Yu |
collection | PubMed |
description | Dectin-1, a classical pattern-recognition receptor, was now identified as an important regulator in immune homeostasis and cancer immunity through its extensive ligands binding functions and subsequent cytokines production. The aim of this study was to assess the clinical significance of dectin-1 expression in 290 patients with clear cell renal cell carcinoma (ccRCC) through immunohistochemistry on tissue microarrays. We found that dectin-1 was predominantly expressed on ccRCC cells, in accordance with several other online databases. Moreover, Kaplan-Meier method was conducted and high expression of tumoral dectin-1 was associated with shorter patient recurrence free survival (RFS) and overall survival (OS) (P < 0.001 for both). In multivariate analyses, tumoral dectin-1 expression was also confirmed as an independent prognostic factor for patients’ survival together with other clinical parameters (P < 0.001 for RFS and OS). After incorporating these characteristics including tumoral dectin-1 expression, two nomograms were constructed to predict ccRCC patients’ RFS and OS (c-index 0.796 and 0.812, respectively) and performed better than existed integrated models (P < 0.001 for all models comparisons). In conclusion, high tumoral dectin-1 expression was an independent predictor of adverse clinical outcome in ccRCC patients. This molecule and established nomograms might help clinicians in future decision making and therapeutic developments. |
format | Online Article Text |
id | pubmed-5013447 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-50134472016-09-12 Dectin-1 predicts adverse postoperative prognosis of patients with clear cell renal cell carcinoma Xia, Yu Liu, Li Bai, Qi Wang, Jiajun Xi, Wei Qu, Yang Xiong, Ying Long, Qilai Xu, Jiejie Guo, Jianming Sci Rep Article Dectin-1, a classical pattern-recognition receptor, was now identified as an important regulator in immune homeostasis and cancer immunity through its extensive ligands binding functions and subsequent cytokines production. The aim of this study was to assess the clinical significance of dectin-1 expression in 290 patients with clear cell renal cell carcinoma (ccRCC) through immunohistochemistry on tissue microarrays. We found that dectin-1 was predominantly expressed on ccRCC cells, in accordance with several other online databases. Moreover, Kaplan-Meier method was conducted and high expression of tumoral dectin-1 was associated with shorter patient recurrence free survival (RFS) and overall survival (OS) (P < 0.001 for both). In multivariate analyses, tumoral dectin-1 expression was also confirmed as an independent prognostic factor for patients’ survival together with other clinical parameters (P < 0.001 for RFS and OS). After incorporating these characteristics including tumoral dectin-1 expression, two nomograms were constructed to predict ccRCC patients’ RFS and OS (c-index 0.796 and 0.812, respectively) and performed better than existed integrated models (P < 0.001 for all models comparisons). In conclusion, high tumoral dectin-1 expression was an independent predictor of adverse clinical outcome in ccRCC patients. This molecule and established nomograms might help clinicians in future decision making and therapeutic developments. Nature Publishing Group 2016-09-07 /pmc/articles/PMC5013447/ /pubmed/27600310 http://dx.doi.org/10.1038/srep32657 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Xia, Yu Liu, Li Bai, Qi Wang, Jiajun Xi, Wei Qu, Yang Xiong, Ying Long, Qilai Xu, Jiejie Guo, Jianming Dectin-1 predicts adverse postoperative prognosis of patients with clear cell renal cell carcinoma |
title | Dectin-1 predicts adverse postoperative prognosis of patients with clear cell renal cell carcinoma |
title_full | Dectin-1 predicts adverse postoperative prognosis of patients with clear cell renal cell carcinoma |
title_fullStr | Dectin-1 predicts adverse postoperative prognosis of patients with clear cell renal cell carcinoma |
title_full_unstemmed | Dectin-1 predicts adverse postoperative prognosis of patients with clear cell renal cell carcinoma |
title_short | Dectin-1 predicts adverse postoperative prognosis of patients with clear cell renal cell carcinoma |
title_sort | dectin-1 predicts adverse postoperative prognosis of patients with clear cell renal cell carcinoma |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5013447/ https://www.ncbi.nlm.nih.gov/pubmed/27600310 http://dx.doi.org/10.1038/srep32657 |
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