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A panel containing PD-1, IL-2Rα, IL-10, and CA15-3 as a biomarker to discriminate breast cancer from benign breast disease
INTRODUCTION: Programmed cell death protein 1 (PD-1), an immune checkpoint molecule, has recently been recognized as a predictive and prognostic biomarker in several malignant tumors, but its diagnostic value remains largely unknown. We aimed to investigate the differential diagnostic efficiency of...
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/PMC6027692/ https://www.ncbi.nlm.nih.gov/pubmed/29983594 http://dx.doi.org/10.2147/CMAR.S160452 |
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author | Liu, Chao Sun, Bing Xu, Bin Meng, Xiangying Li, Lan Cong, Yang Liu, Jiannan Wang, Qian Xuan, Liang Song, Qibin Wu, Shikai |
author_facet | Liu, Chao Sun, Bing Xu, Bin Meng, Xiangying Li, Lan Cong, Yang Liu, Jiannan Wang, Qian Xuan, Liang Song, Qibin Wu, Shikai |
author_sort | Liu, Chao |
collection | PubMed |
description | INTRODUCTION: Programmed cell death protein 1 (PD-1), an immune checkpoint molecule, has recently been recognized as a predictive and prognostic biomarker in several malignant tumors, but its diagnostic value remains largely unknown. We aimed to investigate the differential diagnostic efficiency of PD-1 and other immune molecules and propose a panel of immune molecules combined with cancer antigen 15-3 (CA15-3) to distinguish breast cancer (BC) from benign breast disease (BBD). PATIENTS AND METHODS: Ninety-one eligible BC patients and 31 BBD patients were enrolled. Pretreatment peripheral blood was collected and tested for mRNA expression of PD-1, cytotoxic T lymphocyte antigen 4, forkhead box P3, transforming growth factor beta, interleukin-10 (IL-10), IL-2 receptor alpha (IL-2Rα), and cluster of differentiation 28 by quantitative reverse transcription PCR. RESULTS: The diagnostic areas under curve (AUCs) of PD-1, IL-2Rα, and IL-10 for BC–BBD discrimination were 0.764, 0.758, and 0.743, respectively. The diagnostic efficiencies of these three parameters in distinguishing early-stage or advanced BC from BBD were consistent with a role in BC–BBD discrimination. A panel of PD-1 + IL-10 + IL-2Rα + CA15-3 showed the highest AUC (0.862), with a sensitivity of 0.933 and a specificity of 0.724, for BC–BBD discrimination. In addition, for early-stage BC discrimination, this panel also had the highest AUC (0.811), with a sensitivity of 0.933 and a specificity of 0.614, while for advanced BC discrimination, a panel of PD-1 + IL-10 + CA15-3 exhibited the highest AUC (0.896), with a sensitivity of 0.933 and a specificity of 0.783. CONCLUSION: These data indicate that the panel containing PD-1, IL-2Rα, IL-10, and CA15-3 can effectively discriminate BC from BBD with a high efficiency. After further confirmation, it could be used to complement conventional imaging modalities, especially in discriminating early-stage BC from BBD. |
format | Online Article Text |
id | pubmed-6027692 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-60276922018-07-06 A panel containing PD-1, IL-2Rα, IL-10, and CA15-3 as a biomarker to discriminate breast cancer from benign breast disease Liu, Chao Sun, Bing Xu, Bin Meng, Xiangying Li, Lan Cong, Yang Liu, Jiannan Wang, Qian Xuan, Liang Song, Qibin Wu, Shikai Cancer Manag Res Original Research INTRODUCTION: Programmed cell death protein 1 (PD-1), an immune checkpoint molecule, has recently been recognized as a predictive and prognostic biomarker in several malignant tumors, but its diagnostic value remains largely unknown. We aimed to investigate the differential diagnostic efficiency of PD-1 and other immune molecules and propose a panel of immune molecules combined with cancer antigen 15-3 (CA15-3) to distinguish breast cancer (BC) from benign breast disease (BBD). PATIENTS AND METHODS: Ninety-one eligible BC patients and 31 BBD patients were enrolled. Pretreatment peripheral blood was collected and tested for mRNA expression of PD-1, cytotoxic T lymphocyte antigen 4, forkhead box P3, transforming growth factor beta, interleukin-10 (IL-10), IL-2 receptor alpha (IL-2Rα), and cluster of differentiation 28 by quantitative reverse transcription PCR. RESULTS: The diagnostic areas under curve (AUCs) of PD-1, IL-2Rα, and IL-10 for BC–BBD discrimination were 0.764, 0.758, and 0.743, respectively. The diagnostic efficiencies of these three parameters in distinguishing early-stage or advanced BC from BBD were consistent with a role in BC–BBD discrimination. A panel of PD-1 + IL-10 + IL-2Rα + CA15-3 showed the highest AUC (0.862), with a sensitivity of 0.933 and a specificity of 0.724, for BC–BBD discrimination. In addition, for early-stage BC discrimination, this panel also had the highest AUC (0.811), with a sensitivity of 0.933 and a specificity of 0.614, while for advanced BC discrimination, a panel of PD-1 + IL-10 + CA15-3 exhibited the highest AUC (0.896), with a sensitivity of 0.933 and a specificity of 0.783. CONCLUSION: These data indicate that the panel containing PD-1, IL-2Rα, IL-10, and CA15-3 can effectively discriminate BC from BBD with a high efficiency. After further confirmation, it could be used to complement conventional imaging modalities, especially in discriminating early-stage BC from BBD. Dove Medical Press 2018-06-26 /pmc/articles/PMC6027692/ /pubmed/29983594 http://dx.doi.org/10.2147/CMAR.S160452 Text en © 2018 Liu 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 Liu, Chao Sun, Bing Xu, Bin Meng, Xiangying Li, Lan Cong, Yang Liu, Jiannan Wang, Qian Xuan, Liang Song, Qibin Wu, Shikai A panel containing PD-1, IL-2Rα, IL-10, and CA15-3 as a biomarker to discriminate breast cancer from benign breast disease |
title | A panel containing PD-1, IL-2Rα, IL-10, and CA15-3 as a biomarker
to discriminate breast cancer from benign breast disease |
title_full | A panel containing PD-1, IL-2Rα, IL-10, and CA15-3 as a biomarker
to discriminate breast cancer from benign breast disease |
title_fullStr | A panel containing PD-1, IL-2Rα, IL-10, and CA15-3 as a biomarker
to discriminate breast cancer from benign breast disease |
title_full_unstemmed | A panel containing PD-1, IL-2Rα, IL-10, and CA15-3 as a biomarker
to discriminate breast cancer from benign breast disease |
title_short | A panel containing PD-1, IL-2Rα, IL-10, and CA15-3 as a biomarker
to discriminate breast cancer from benign breast disease |
title_sort | panel containing pd-1, il-2rα, il-10, and ca15-3 as a biomarker
to discriminate breast cancer from benign breast disease |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6027692/ https://www.ncbi.nlm.nih.gov/pubmed/29983594 http://dx.doi.org/10.2147/CMAR.S160452 |
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