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Carcinoembryonic antigen as a marker of radioresistance in colorectal cancer: a potential role of macrophages

BACKGROUND: We sought to identify the carcinoembryonic antigen (CEA) as a marker of radioresistance in rectal cancer. METHODS: From July 1997 to January 2008, 104 patients with stage II or III rectal cancer who were treated with post-operative radiotherapy (PORT) were included in this study. The dos...

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Autores principales: Huang, Eng-Yen, Chang, Jen-Chieh, Chen, Hong-Hwa, Hsu, Chieh-Ying, Hsu, Hsuan-Chih, Wu, Keng-Liang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5870371/
https://www.ncbi.nlm.nih.gov/pubmed/29580202
http://dx.doi.org/10.1186/s12885-018-4254-4
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author Huang, Eng-Yen
Chang, Jen-Chieh
Chen, Hong-Hwa
Hsu, Chieh-Ying
Hsu, Hsuan-Chih
Wu, Keng-Liang
author_facet Huang, Eng-Yen
Chang, Jen-Chieh
Chen, Hong-Hwa
Hsu, Chieh-Ying
Hsu, Hsuan-Chih
Wu, Keng-Liang
author_sort Huang, Eng-Yen
collection PubMed
description BACKGROUND: We sought to identify the carcinoembryonic antigen (CEA) as a marker of radioresistance in rectal cancer. METHODS: From July 1997 to January 2008, 104 patients with stage II or III rectal cancer who were treated with post-operative radiotherapy (PORT) were included in this study. The doses of radiotherapy ranged from 45 to 54.6 Gy. The CEA levels were measured before surgery. We analyzed the actuarial rates of overall survival (OS), distant metastasis (DM), and local recurrence (LR) using Kaplan-Meier curves. Multivariate analyses were performed with Cox regression models. We used THP-1 monocyte cell lines for macrophage differentiation (M0, M1 or M2). The RNA extracted from the macrophages was analyzed via a genomic method in the core laboratory. The radiosensitivities of CEA-rich LS1034 cells were compared between cells with and without the conditioned media from CEA-stimulated macrophages. RESULTS: Preoperative CEA levels ≥10 ng/mL were independent predictive factors for OS (p = 0.005), DM (p = 0.026), and LR (p = 0.004). The OS rates among the patients with pretreatment CEA levels < 10 ng/mL and ≥10 ng/mL were 64.5% and 35.9% (p = 0.004), respectively. The corresponding rates of DM were 40.6% and 73.1% (p = 0.024). The corresponding rates of LR were 6.6% and 33.9% (p = 0.002). In the M0 macrophages, exogenous CEA elicited a dose-response relationship with M2 differentiation. In the CEA-stimulated M0 cells, some mRNAs were upregulated by as much as 5-fold, including MMP12, GDF15, and JAG1. In the CEA-stimulated M2 cells, a 4-fold up-regulation of GADD45G mRNA was noted. The conditioned media from the CEA-stimulated M2 cells elicited an increase in the numbers of LS180, SW620, and LS1034 cells after irradiation. CEA caused the M2 differentiation of the macrophages. CONCLUSION: Pretreatment CEA levels ≥10 ng/mL are a significant risk factor for OS, DM, and LR following PORT for rectal cancer. CEA causes radioresistance in the presence of M2 macrophages. More comprehensive examinations prior to surgery and intensive adjuvant therapy are suggested for patients with CEA levels ≥10 ng/mL. Further studies of these mechanisms are needed.
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spelling pubmed-58703712018-03-29 Carcinoembryonic antigen as a marker of radioresistance in colorectal cancer: a potential role of macrophages Huang, Eng-Yen Chang, Jen-Chieh Chen, Hong-Hwa Hsu, Chieh-Ying Hsu, Hsuan-Chih Wu, Keng-Liang BMC Cancer Research Article BACKGROUND: We sought to identify the carcinoembryonic antigen (CEA) as a marker of radioresistance in rectal cancer. METHODS: From July 1997 to January 2008, 104 patients with stage II or III rectal cancer who were treated with post-operative radiotherapy (PORT) were included in this study. The doses of radiotherapy ranged from 45 to 54.6 Gy. The CEA levels were measured before surgery. We analyzed the actuarial rates of overall survival (OS), distant metastasis (DM), and local recurrence (LR) using Kaplan-Meier curves. Multivariate analyses were performed with Cox regression models. We used THP-1 monocyte cell lines for macrophage differentiation (M0, M1 or M2). The RNA extracted from the macrophages was analyzed via a genomic method in the core laboratory. The radiosensitivities of CEA-rich LS1034 cells were compared between cells with and without the conditioned media from CEA-stimulated macrophages. RESULTS: Preoperative CEA levels ≥10 ng/mL were independent predictive factors for OS (p = 0.005), DM (p = 0.026), and LR (p = 0.004). The OS rates among the patients with pretreatment CEA levels < 10 ng/mL and ≥10 ng/mL were 64.5% and 35.9% (p = 0.004), respectively. The corresponding rates of DM were 40.6% and 73.1% (p = 0.024). The corresponding rates of LR were 6.6% and 33.9% (p = 0.002). In the M0 macrophages, exogenous CEA elicited a dose-response relationship with M2 differentiation. In the CEA-stimulated M0 cells, some mRNAs were upregulated by as much as 5-fold, including MMP12, GDF15, and JAG1. In the CEA-stimulated M2 cells, a 4-fold up-regulation of GADD45G mRNA was noted. The conditioned media from the CEA-stimulated M2 cells elicited an increase in the numbers of LS180, SW620, and LS1034 cells after irradiation. CEA caused the M2 differentiation of the macrophages. CONCLUSION: Pretreatment CEA levels ≥10 ng/mL are a significant risk factor for OS, DM, and LR following PORT for rectal cancer. CEA causes radioresistance in the presence of M2 macrophages. More comprehensive examinations prior to surgery and intensive adjuvant therapy are suggested for patients with CEA levels ≥10 ng/mL. Further studies of these mechanisms are needed. BioMed Central 2018-03-27 /pmc/articles/PMC5870371/ /pubmed/29580202 http://dx.doi.org/10.1186/s12885-018-4254-4 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Huang, Eng-Yen
Chang, Jen-Chieh
Chen, Hong-Hwa
Hsu, Chieh-Ying
Hsu, Hsuan-Chih
Wu, Keng-Liang
Carcinoembryonic antigen as a marker of radioresistance in colorectal cancer: a potential role of macrophages
title Carcinoembryonic antigen as a marker of radioresistance in colorectal cancer: a potential role of macrophages
title_full Carcinoembryonic antigen as a marker of radioresistance in colorectal cancer: a potential role of macrophages
title_fullStr Carcinoembryonic antigen as a marker of radioresistance in colorectal cancer: a potential role of macrophages
title_full_unstemmed Carcinoembryonic antigen as a marker of radioresistance in colorectal cancer: a potential role of macrophages
title_short Carcinoembryonic antigen as a marker of radioresistance in colorectal cancer: a potential role of macrophages
title_sort carcinoembryonic antigen as a marker of radioresistance in colorectal cancer: a potential role of macrophages
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5870371/
https://www.ncbi.nlm.nih.gov/pubmed/29580202
http://dx.doi.org/10.1186/s12885-018-4254-4
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