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Interleukin-35 as a predictor of prostate cancer in patients undergoing initial prostate biopsy
BACKGROUND: Interleukin (IL)-35 is a novel inhibitory cytokine and has recently been implicated in tumor immunity. However, the role of IL-35 in prostate cancer (PCa) has not been elucidated. OBJECTIVE: To evaluate the role of plasma IL-35 in the diagnosis and prognosis of PCa in Chinese patients un...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5522820/ https://www.ncbi.nlm.nih.gov/pubmed/28761357 http://dx.doi.org/10.2147/OTT.S135873 |
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author | Zhou, Chenchao Zhang, Jun Chen, Ye Wang, Hao Hou, Jianquan |
author_facet | Zhou, Chenchao Zhang, Jun Chen, Ye Wang, Hao Hou, Jianquan |
author_sort | Zhou, Chenchao |
collection | PubMed |
description | BACKGROUND: Interleukin (IL)-35 is a novel inhibitory cytokine and has recently been implicated in tumor immunity. However, the role of IL-35 in prostate cancer (PCa) has not been elucidated. OBJECTIVE: To evaluate the role of plasma IL-35 in the diagnosis and prognosis of PCa in Chinese patients undergoing initial prostate biopsy. MATERIALS AND METHODS: Using ELISA, plasma IL-35 levels were measured in 180 patients, who underwent a prostate biopsy. The clinical correlation of IL-35 with clinicopathological parameters was also evaluated. Univariate and multivariate logistic regression and receiver operating characteristic (ROC) curve analysis were performed to establish the role of IL-35 as a clinical biomarker. RESULTS: Seventy-five (41.6%) of patients were histopathologically confirmed to have PCa. Plasma IL-35 levels were significantly higher in PCa patients (134.48±78.48 pg/mL) compared to non-PCa patients (67.22±24.08 pg/mL). ROC analysis showed that IL-35 was an independent predictor of PCa. Furthermore, IL-35 was found to be a significantly independent predictor of PCa in a group of patients with prostate-specific antigen levels between 4 and 10 ng/mL; was also able to predict advanced PCa from localized PCa and bone metastasis positive PCa from negative PCa. CONCLUSION: Our data suggest for the first time that plasma IL-35 levels are correlated with PCa and is the independent predictor of PCa progression and metastasis. Thus, IL-35 could be utilized as a potential biomarker for diagnosis and prognosis of PCa, could also aid in decision making and predict the stage of the disease. |
format | Online Article Text |
id | pubmed-5522820 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-55228202017-07-31 Interleukin-35 as a predictor of prostate cancer in patients undergoing initial prostate biopsy Zhou, Chenchao Zhang, Jun Chen, Ye Wang, Hao Hou, Jianquan Onco Targets Ther Original Research BACKGROUND: Interleukin (IL)-35 is a novel inhibitory cytokine and has recently been implicated in tumor immunity. However, the role of IL-35 in prostate cancer (PCa) has not been elucidated. OBJECTIVE: To evaluate the role of plasma IL-35 in the diagnosis and prognosis of PCa in Chinese patients undergoing initial prostate biopsy. MATERIALS AND METHODS: Using ELISA, plasma IL-35 levels were measured in 180 patients, who underwent a prostate biopsy. The clinical correlation of IL-35 with clinicopathological parameters was also evaluated. Univariate and multivariate logistic regression and receiver operating characteristic (ROC) curve analysis were performed to establish the role of IL-35 as a clinical biomarker. RESULTS: Seventy-five (41.6%) of patients were histopathologically confirmed to have PCa. Plasma IL-35 levels were significantly higher in PCa patients (134.48±78.48 pg/mL) compared to non-PCa patients (67.22±24.08 pg/mL). ROC analysis showed that IL-35 was an independent predictor of PCa. Furthermore, IL-35 was found to be a significantly independent predictor of PCa in a group of patients with prostate-specific antigen levels between 4 and 10 ng/mL; was also able to predict advanced PCa from localized PCa and bone metastasis positive PCa from negative PCa. CONCLUSION: Our data suggest for the first time that plasma IL-35 levels are correlated with PCa and is the independent predictor of PCa progression and metastasis. Thus, IL-35 could be utilized as a potential biomarker for diagnosis and prognosis of PCa, could also aid in decision making and predict the stage of the disease. Dove Medical Press 2017-07-14 /pmc/articles/PMC5522820/ /pubmed/28761357 http://dx.doi.org/10.2147/OTT.S135873 Text en © 2017 Zhou 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 Zhou, Chenchao Zhang, Jun Chen, Ye Wang, Hao Hou, Jianquan Interleukin-35 as a predictor of prostate cancer in patients undergoing initial prostate biopsy |
title | Interleukin-35 as a predictor of prostate cancer in patients undergoing initial prostate biopsy |
title_full | Interleukin-35 as a predictor of prostate cancer in patients undergoing initial prostate biopsy |
title_fullStr | Interleukin-35 as a predictor of prostate cancer in patients undergoing initial prostate biopsy |
title_full_unstemmed | Interleukin-35 as a predictor of prostate cancer in patients undergoing initial prostate biopsy |
title_short | Interleukin-35 as a predictor of prostate cancer in patients undergoing initial prostate biopsy |
title_sort | interleukin-35 as a predictor of prostate cancer in patients undergoing initial prostate biopsy |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5522820/ https://www.ncbi.nlm.nih.gov/pubmed/28761357 http://dx.doi.org/10.2147/OTT.S135873 |
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