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

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          Abstract

          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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          Most cited references32

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          Macrophages in Tumor Microenvironments and the Progression of Tumors

          Macrophages are widely distributed innate immune cells that play indispensable roles in the innate and adaptive immune response to pathogens and in-tissue homeostasis. Macrophages can be activated by a variety of stimuli and polarized to functionally different phenotypes. Two distinct subsets of macrophages have been proposed, including classically activated (M1) and alternatively activated (M2) macrophages. M1 macrophages express a series of proinflammatory cytokines, chemokines, and effector molecules, such as IL-12, IL-23, TNF- α , iNOS and MHCI/II. In contrast, M2 macrophages express a wide array of anti-inflammatory molecules, such as IL-10, TGF- β , and arginase1. In most tumors, the infiltrated macrophages are considered to be of the M2 phenotype, which provides an immunosuppressive microenvironment for tumor growth. Furthermore, tumor-associated macrophages secrete many cytokines, chemokines, and proteases, which promote tumor angiogenesis, growth, metastasis, and immunosuppression. Recently, it was also found that tumor-associated macrophages interact with cancer stem cells. This interaction leads to tumorigenesis, metastasis, and drug resistance. So mediating macrophage to resist tumors is considered to be potential therapy.
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            Endothelial cells promote the colorectal cancer stem cell phenotype through a soluble form of Jagged-1.

            We report a paracrine effect whereby endothelial cells (ECs) promote the cancer stem cell (CSC) phenotype of human colorectal cancer (CRC) cells. We showed that, without direct cell-cell contact, ECs secrete factors that promoted the CSC phenotype in CRC cells via Notch activation. In human CRC specimens, CD133 and Notch intracellular domain-positive CRC cells colocalized in perivascular regions. An EC-derived, soluble form of Jagged-1, via ADAM17 proteolytic activity, led to Notch activation in CRC cells in a paracrine manner; these effects were blocked by immunodepletion of Jagged-1 in EC-conditioned medium or blockade of ADAM17 activity. Collectively, ECs play an active role in promoting Notch signaling and the CSC phenotype by secreting soluble Jagged-1. Copyright © 2013 Elsevier Inc. All rights reserved.
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              Tumor-associated macrophages in breast cancer: distinct subsets, distinct functions.

              Macrophages display remarkable plasticity, allowing these cells to adapt to changing microenvironments and perform functions as diverse as tissue development and homeostasis, inflammation, pathogen clearance and wound healing. Macrophage activation can be triggered by Th1 cytokines and pathogen-associated or endogenous danger signals, leading to the formation of classically activated or M1 macrophages. On the other hand, anti-inflammatory mediators, including IL-4, IL-10, TGF-β and M-CSF, induce diverse anti-inflammatory types of macrophages, known under the generic term M2. In human breast carcinomas, tumor-associated macrophage (TAM) density correlates with poor prognosis. In mouse models of breast cancer, eliminating macrophages from the tumor site, either via genetic or therapeutic means, results in retarded tumor progression. Over the years, multiple signals from the mammary tumor microenvironment have been reported to influence the TAM phenotype and TAM have been propagated as anti-inflammatory M2-like cells. Recent developments point to the existence of at least two distinct TAM subpopulations in mammary tumors, based on a differential expression of markers such as CD206 or MHC II and different in vivo behaviour: perivascular, migratory TAM which are less M2-like, and sessile TAM found at tumor-stroma borders and/or hypoxic regions that resemble more M2-like or "trophic" macrophages. Hence, a further refinement of the molecular and functional heterogeneity of TAM is an avenue for further research, with a potential impact on the usefulness of these cells as therapeutic targets.
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                Author and article information

                Contributors
                huangengyen@gmail.com
                rj_chang@yahoo.com.tw
                hey1200@seed.net.tw
                hsuan5@adm.cgmh.org.tw
                xavier_jay@hotmail.com
                kengliang_wu@yahoo.com.tw
                Journal
                BMC Cancer
                BMC Cancer
                BMC Cancer
                BioMed Central (London )
                1471-2407
                27 March 2018
                27 March 2018
                2018
                : 18
                : 321
                Affiliations
                [1 ]GRID grid.413804.a, Department of Radiation Oncology, , Kaohsiung Chang Gung Memorial Hospital, Chang Gung University College of Medicine, ; Kaohsiung, Taiwan
                [2 ]GRID grid.145695.a, School of Traditional Chinese Medicine, , Chang Gung University College of Medicine, ; Kaohsiung, Taiwan
                [3 ]GRID grid.413804.a, Department of Medical Research, , Kaohsiung Chang Gung Memorial Hospital, Chang Gung University College of Medicine, ; Kaohsiung, Taiwan
                [4 ]GRID grid.413804.a, Division of Colonic and Rectal Surgery, Department of Surgery, , Kaohsiung Chang Gung Memorial Hospital, Chang Gung University College of Medicine, ; Kaohsiung, Taiwan
                [5 ]GRID grid.413804.a, Division of Hepatogastroenterology, Department of Internal Medicine, , Kaohsiung Chang Gung Memorial Hospital, Chang Gung University College of Medicine, ; Kaohsiung, Taiwan
                Author information
                http://orcid.org/0000-0002-2041-0782
                Article
                4254
                10.1186/s12885-018-4254-4
                5870371
                29580202
                e8fea362-781e-47b6-abf0-af491ebafdba
                © 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.

                History
                : 15 February 2017
                : 20 March 2018
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/501100004606, Chang Gung Medical Foundation;
                Award ID: CMRPG8B1141
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/501100001868, National Science Council;
                Award ID: NSC100~102-2325-B-182-004-
                Award Recipient :
                Categories
                Research Article
                Custom metadata
                © The Author(s) 2018

                Oncology & Radiotherapy
                rectal cancer,carcinoembryonic antigen,radiotherapy,macrophage,radioresistance

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