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We are analyzing https://link.springer.com/article/10.1007/s00262-020-02567-y.

Title:
Comparative immunomodulatory properties of mesenchymal stem cells derived from human breast tumor and normal breast adipose tissue | Cancer Immunology, Immunotherapy
Description:
Objective Mesenchymal stem cells (MSCs), one of the most important stromal cells in the tumor microenvironment, play a major role in the immunomodulation and development of tumors. In contrast to immunomodulatory effects of bone marrow-derived MSCs, resident MSCs were not well studied in tumor. The aim of this study was to compare the immunomodulatory properties and protein secretion profiles of MSCs isolated from breast tumor (T-MSC) and normal breast adipose tissue (N-MSC). Materials and methods T-MSCs and N-MSCs were isolated by the explant culture method and characterized, and their immunomodulatory function was assessed on peripheral blood lymphocytes (PBLs) by evaluating the effects of MSC conditioned media on the proliferation and induction of some cytokines and regulatory T cells (Tregs) by BrdU assay, ELISA, and flow cytometry. In addition, we compared the secretion of indoleamine 2,3-dioxygenase (IDO), vascular endothelial growth factor (VEGF), matrix metallopeptidase (MMP)-2, MMP-9, and Galectin-1. Results T-MSCs showed a higher secretion of transforming growth factor beta (TGF-β), prostaglandin E2 (PGE2), IDO, and VEGF and lower secretion of MMP-2 and MMP-9 compared with N-MSCs. However, no significant difference was found in the secretion of interferon gamma (IFN-γ), interleukin 10 (IL10), IL4, IL17, and Galectin-1 in T-MSCs and N-MSCs. The immunomodulatory effect of soluble factors on PBLs showed that T-MSCs, in contrast to N-MSCs, stimulate PBL proliferation. Importantly, the ability of T-MSCs to induce IL10, TGF-β, IFN-γ, and PGE2 was higher than that of N-MSCs. In addition, T-MSCs and N-MSCs exhibited no significant difference in Treg induction. Conclusion MSCs educated in stage II breast cancer and normal breast adipose tissue, although sharing a similar morphology and immunophenotype, exhibited a clearly different profile in some immunomodulatory functions and protein secretions.
Website Age:
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  • Science
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Custom-built

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🌠 Phenomenal Traffic: 5M - 10M visitors per month


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Keywords {🔍}

cells, article, pubmed, google, scholar, stem, mesenchymal, cancer, cell, cas, breast, immunomodulatory, tumor, central, sciences, iran, human, tehran, university, medical, research, stromal, effects, adipose, res, hashemi, mscs, microenvironment, secretion, regulatory, tissue, seyed, mahmoud, tmscs, nmscs, springer, privacy, cookies, content, immunology, derived, normal, sineh, sepehr, razavi, proliferation, growth, factor, mmp, galectin,

Topics {✒️}

month download article/chapter seyed mahmoud hashemi mesenchymal stem cells-basics mesenchymal stroma/stem cells anti-inflammatory regulatory t-cell bone marrow-derived mscs meghdad abdollahpour-alitappeh pi3k/akt/mtor pathway mesenchymal stem cells t-cell effector pathways therapy-related myeloid neoplasms mir saeed yekaninejad mesenchymal stromal cells zuhair mohammad hassan regulatory t-cell expansion breast cancer cells article cancer immunology jelly stem cell important stromal cells systemic immunomodulatory factor full article pdf protein secretion profiles privacy choices/manage cookies breast cancer patients naive t-cells majid mossahebi-mohammadi human breast tumor tumor microenvironment immunostimulant colorectal tumor microenvironment stem cells stem cells 6 comparative immunomodulatory properties tumor cells crosstalk abdollahpour-alitappeh increase treg cells bmc cancer 18 targeting tumor microenvironment mcf-7 cell line sineh sepehr author information authors immunomodulation-related cytokines expression profile bone marrow clinical application ii acute lung injury t-cell proliferation applied cell sciences related subjects peripheral blood lymphocytes treg/th17 polarization

Schema {🗺️}

WebPage:
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         description:Mesenchymal stem cells (MSCs), one of the most important stromal cells in the tumor microenvironment, play a major role in the immunomodulation and development of tumors. In contrast to immunomodulatory effects of bone marrow-derived MSCs, resident MSCs were not well studied in tumor. The aim of this study was to compare the immunomodulatory properties and protein secretion profiles of MSCs isolated from breast tumor (T-MSC) and normal breast adipose tissue (N-MSC). T-MSCs and N-MSCs were isolated by the explant culture method and characterized, and their immunomodulatory function was assessed on peripheral blood lymphocytes (PBLs) by evaluating the effects of MSC conditioned media on the proliferation and induction of some cytokines and regulatory T cells (Tregs) by BrdU assay, ELISA, and flow cytometry. In addition, we compared the secretion of indoleamine 2,3-dioxygenase (IDO), vascular endothelial growth factor (VEGF), matrix metallopeptidase (MMP)-2, MMP-9, and Galectin-1. T-MSCs showed a higher secretion of transforming growth factor beta (TGF-β), prostaglandin E2 (PGE2), IDO, and VEGF and lower secretion of MMP-2 and MMP-9 compared with N-MSCs. However, no significant difference was found in the secretion of interferon gamma (IFN-γ), interleukin 10 (IL10), IL4, IL17, and Galectin-1 in T-MSCs and N-MSCs. The immunomodulatory effect of soluble factors on PBLs showed that T-MSCs, in contrast to N-MSCs, stimulate PBL proliferation. Importantly, the ability of T-MSCs to induce IL10, TGF-β, IFN-γ, and PGE2 was higher than that of N-MSCs. In addition, T-MSCs and N-MSCs exhibited no significant difference in Treg induction. MSCs educated in stage II breast cancer and normal breast adipose tissue, although sharing a similar morphology and immunophenotype, exhibited a clearly different profile in some immunomodulatory functions and protein secretions.
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      headline:Comparative immunomodulatory properties of mesenchymal stem cells derived from human breast tumor and normal breast adipose tissue
      description:Mesenchymal stem cells (MSCs), one of the most important stromal cells in the tumor microenvironment, play a major role in the immunomodulation and development of tumors. In contrast to immunomodulatory effects of bone marrow-derived MSCs, resident MSCs were not well studied in tumor. The aim of this study was to compare the immunomodulatory properties and protein secretion profiles of MSCs isolated from breast tumor (T-MSC) and normal breast adipose tissue (N-MSC). T-MSCs and N-MSCs were isolated by the explant culture method and characterized, and their immunomodulatory function was assessed on peripheral blood lymphocytes (PBLs) by evaluating the effects of MSC conditioned media on the proliferation and induction of some cytokines and regulatory T cells (Tregs) by BrdU assay, ELISA, and flow cytometry. In addition, we compared the secretion of indoleamine 2,3-dioxygenase (IDO), vascular endothelial growth factor (VEGF), matrix metallopeptidase (MMP)-2, MMP-9, and Galectin-1. T-MSCs showed a higher secretion of transforming growth factor beta (TGF-β), prostaglandin E2 (PGE2), IDO, and VEGF and lower secretion of MMP-2 and MMP-9 compared with N-MSCs. However, no significant difference was found in the secretion of interferon gamma (IFN-γ), interleukin 10 (IL10), IL4, IL17, and Galectin-1 in T-MSCs and N-MSCs. The immunomodulatory effect of soluble factors on PBLs showed that T-MSCs, in contrast to N-MSCs, stimulate PBL proliferation. Importantly, the ability of T-MSCs to induce IL10, TGF-β, IFN-γ, and PGE2 was higher than that of N-MSCs. In addition, T-MSCs and N-MSCs exhibited no significant difference in Treg induction. MSCs educated in stage II breast cancer and normal breast adipose tissue, although sharing a similar morphology and immunophenotype, exhibited a clearly different profile in some immunomodulatory functions and protein secretions.
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         Mesenchymal stem cells (MSCs)
         Breast cancer
         Immunomodulatory
         Oncology
         Immunology
         Cancer Research
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      name:Cancer Research Center, Golestan University of Medical Sciences, Gorgan, Iran
      name:Cellular and Molecular Biology Research Center, Larestan University of Medical Sciences, Larestan, Iran
      name:Sarem Cell Research Center(SCRC), Sarem Women’s Hospital, Tehran, Iran
      name:Department of Epidemiology and Biostatistics, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran
      name:Neuroscience Research Center (NRC), Iran University of Medical Sciences, Tehran, Iran
      name:Department of Immunology, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran
      name:Urogenital Stem Cell Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran
      name:Department of Tissue Engineering and Applied Cell Sciences, School of Advanced Technologies in Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran
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