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Prognostic value of diametrically polarized tumor-associated macrophages in multiple myeloma
Tumor-associated macrophages (TAMs) are correlated with the prognosis of different types of solid tumors and lymphoma, according to many clinical studies. In vitro experiments have demonstrated the roles of these cells in myeloma cell survival, angiogenesis, immunomodulation, drug resistance, and th...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5762541/ https://www.ncbi.nlm.nih.gov/pubmed/29348856 http://dx.doi.org/10.18632/oncotarget.22340 |
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author | Chen, Xinyi Chen, Jin Zhang, Wenyan Sun, Ruixue Liu, Ting Zheng, Yuhuan Wu, Yu |
author_facet | Chen, Xinyi Chen, Jin Zhang, Wenyan Sun, Ruixue Liu, Ting Zheng, Yuhuan Wu, Yu |
author_sort | Chen, Xinyi |
collection | PubMed |
description | Tumor-associated macrophages (TAMs) are correlated with the prognosis of different types of solid tumors and lymphoma, according to many clinical studies. In vitro experiments have demonstrated the roles of these cells in myeloma cell survival, angiogenesis, immunomodulation, drug resistance, and the interaction between malignant myeloma cells and the microenvironment. Here, we investigated the prognostic significance of TAMs in patients with multiple myeloma (MM). We evaluated the polarized functional status of bone marrow infiltrated by TAMs by immunohistochemical staining of CD68, iNOS, and CD163 in 240 patients with MM from January 2009 to December 2014. The overall response rates to chemotherapy were lower in patients with high CD68(+) or CD163(+) TAM densities than in those with low densities. Kaplan-Meier analysis showed that the progression-free survival (PFS, p = 0.001) and overall survival (OS, p < 0.001) of patients with low CD163(+) TAM density were significantly higher than those of patients with high CD163(+) TAM density. Furthermore, combined analysis of iNOS(+) and CD163(+) TAMs (iNOS/CD163 signature) exhibited greater power in predicting patient outcomes for both PFS (p < 0.001) and OS (p < 0.001). Moreover, Cox regression analysis identified iNOS(+) and CD163(+) TAMs as independent prognostic factors (p = 0.007, p < 0.001, respectively). These factors could be combined with the international staging system (ISS) to generate a predictive nomogram for patient outcomes. Our findings suggest that the mosaic of diametrically polarized TAMs is a novel independent prognostic factor that could be integrated into the evaluation of and therapy for MM. |
format | Online Article Text |
id | pubmed-5762541 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-57625412018-01-18 Prognostic value of diametrically polarized tumor-associated macrophages in multiple myeloma Chen, Xinyi Chen, Jin Zhang, Wenyan Sun, Ruixue Liu, Ting Zheng, Yuhuan Wu, Yu Oncotarget Research Paper Tumor-associated macrophages (TAMs) are correlated with the prognosis of different types of solid tumors and lymphoma, according to many clinical studies. In vitro experiments have demonstrated the roles of these cells in myeloma cell survival, angiogenesis, immunomodulation, drug resistance, and the interaction between malignant myeloma cells and the microenvironment. Here, we investigated the prognostic significance of TAMs in patients with multiple myeloma (MM). We evaluated the polarized functional status of bone marrow infiltrated by TAMs by immunohistochemical staining of CD68, iNOS, and CD163 in 240 patients with MM from January 2009 to December 2014. The overall response rates to chemotherapy were lower in patients with high CD68(+) or CD163(+) TAM densities than in those with low densities. Kaplan-Meier analysis showed that the progression-free survival (PFS, p = 0.001) and overall survival (OS, p < 0.001) of patients with low CD163(+) TAM density were significantly higher than those of patients with high CD163(+) TAM density. Furthermore, combined analysis of iNOS(+) and CD163(+) TAMs (iNOS/CD163 signature) exhibited greater power in predicting patient outcomes for both PFS (p < 0.001) and OS (p < 0.001). Moreover, Cox regression analysis identified iNOS(+) and CD163(+) TAMs as independent prognostic factors (p = 0.007, p < 0.001, respectively). These factors could be combined with the international staging system (ISS) to generate a predictive nomogram for patient outcomes. Our findings suggest that the mosaic of diametrically polarized TAMs is a novel independent prognostic factor that could be integrated into the evaluation of and therapy for MM. Impact Journals LLC 2017-11-09 /pmc/articles/PMC5762541/ /pubmed/29348856 http://dx.doi.org/10.18632/oncotarget.22340 Text en Copyright: © 2017 Chen et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License 3.0 (http://creativecommons.org/licenses/by/3.0/) (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Chen, Xinyi Chen, Jin Zhang, Wenyan Sun, Ruixue Liu, Ting Zheng, Yuhuan Wu, Yu Prognostic value of diametrically polarized tumor-associated macrophages in multiple myeloma |
title | Prognostic value of diametrically polarized tumor-associated macrophages in multiple myeloma |
title_full | Prognostic value of diametrically polarized tumor-associated macrophages in multiple myeloma |
title_fullStr | Prognostic value of diametrically polarized tumor-associated macrophages in multiple myeloma |
title_full_unstemmed | Prognostic value of diametrically polarized tumor-associated macrophages in multiple myeloma |
title_short | Prognostic value of diametrically polarized tumor-associated macrophages in multiple myeloma |
title_sort | prognostic value of diametrically polarized tumor-associated macrophages in multiple myeloma |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5762541/ https://www.ncbi.nlm.nih.gov/pubmed/29348856 http://dx.doi.org/10.18632/oncotarget.22340 |
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