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      Neem leaf glycoprotein prevents post-surgical sarcoma recurrence in Swiss mice by differentially regulating cytotoxic T and myeloid-derived suppressor cells

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          Abstract

          Post-surgical tumor recurrence is a common problem in cancer treatment. In the present study, the role of neem leaf glycoprotein (NLGP), a novel immunomodulator, in prevention of post-surgical recurrence of solid sarcoma was examined. Data suggest that NLGP prevents tumor recurrence after surgical removal of sarcoma in Swiss mice and increases their tumor-free survival time. In NLGP-treated tumor-free mice, increased cytotoxic CD8 + T cells and a decreased population of suppressor cells, especially myeloid-derived suppressor cells (MDSCs) was observed. NLGP-treated CD8 + T cells showed greater cytotoxicity towards tumor-derived MDSCs and supernatants from the same CD8 + T cell culture caused upregulation of FasR and downregulation of cFLIP in MDSCs. To elucidate the role of CD8 + T cells, specifically in association with the downregulation in MDSCs, CD8 + T cells were depleted in vivo before NLGP immunization in surgically tumor removed mice and tumor recurrence was noted. These mice also exhibited increased MDSCs along with decreased levels of Caspase 3, Caspase 8 and increased cFLIP expression. In conclusion, it can be stated that NLGP, by activating CD8 + T cells, down regulates the proportion of MDSCs. Accordingly, suppressive effects of MDSCs on CD8 + T cells are minimized and optimum immune surveillance in tumor hosts is maintained to eliminate the residual tumor mass appearing during recurrence.

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          Molecular mechanisms regulating myeloid-derived suppressor cell differentiation and function.

          Myeloid-derived suppressor cells (MDSCs) are one of the main cell populations responsible for regulating immune responses. MDSCs accumulate during tumor progression, autoimmunity, chronic infection and other pathological conditions, and can potently suppress T cell function. Recent studies have demonstrated the ability of MDSCs to modulate the activity of NK and myeloid cells and have implicated MDSCs in the induction of regulatory T cells. Here, we discuss recent findings that describe the molecular mechanisms that regulate the expansion and function of MDSCs, as well as recent attempts to use MDSCs in cell therapy for different pathologic conditions. Copyright © 2010 Elsevier Ltd. All rights reserved.
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            Inhibition of dendritic cell differentiation and accumulation of myeloid-derived suppressor cells in cancer is regulated by S100A9 protein

            Accumulation of myeloid-derived suppressor cells (MDSCs) associated with inhibition of dendritic cell (DC) differentiation is one of the major immunological abnormalities in cancer and leads to suppression of antitumor immune responses. The molecular mechanism of this phenomenon remains unclear. We report here that STAT3-inducible up-regulation of the myeloid-related protein S100A9 enhances MDSC production in cancer. Mice lacking this protein mounted potent antitumor immune responses and rejected implanted tumors. This effect was reversed by administration of wild-type MDSCs from tumor-bearing mice to S100A9-null mice. Overexpression of S100A9 in cultured embryonic stem cells or transgenic mice inhibited the differentiation of DCs and macrophages and induced accumulation of MDSCs. This study demonstrates that tumor-induced up-regulation of S100A9 protein is critically important for accumulation of MDSCs and reveals a novel molecular mechanism of immunological abnormalities in cancer.
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              Proinflammatory S100 proteins regulate the accumulation of myeloid-derived suppressor cells.

              Chronic inflammation is a complex process that promotes carcinogenesis and tumor progression; however, the mechanisms by which specific inflammatory mediators contribute to tumor growth remain unclear. We and others recently demonstrated that the inflammatory mediators IL-1beta, IL-6, and PGE(2) induce accumulation of myeloid-derived suppressor cells (MDSC) in tumor-bearing individuals. MDSC impair tumor immunity and thereby facilitate carcinogenesis and tumor progression by inhibiting T and NK cell activation, and by polarizing immunity toward a tumor-promoting type 2 phenotype. We now show that this population of immature myeloid cells induced by a given tumor share a common phenotype regardless of their in vivo location (bone marrow, spleen, blood, or tumor site), and that Gr1(high)CD11b(high)F4/80(-)CD80(+)IL4Ralpha(+/-)Arginase(+) MDSC are induced by the proinflammatory proteins S100A8/A9. S100A8/A9 proteins bind to carboxylated N-glycans expressed on the receptor for advanced glycation end-products and other cell surface glycoprotein receptors on MDSC, signal through the NF-kappaB pathway, and promote MDSC migration. MDSC also synthesize and secrete S100A8/A9 proteins that accumulate in the serum of tumor-bearing mice, and in vivo blocking of S100A8/A9 binding to MDSC using an anti-carboxylated glycan Ab reduces MDSC levels in blood and secondary lymphoid organs in mice with metastatic disease. Therefore, the S100 family of inflammatory mediators serves as an autocrine feedback loop that sustains accumulation of MDSC. Since S100A8/A9 activation of MDSC is through the NF-kappaB signaling pathway, drugs that target this pathway may reduce MDSC levels and be useful therapeutic agents in conjunction with active immunotherapy in cancer patients.
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                Author and article information

                Contributors
                Role: Editor
                Journal
                PLoS One
                PLoS ONE
                plos
                plosone
                PLoS ONE
                Public Library of Science (San Francisco, CA USA )
                1932-6203
                17 April 2017
                2017
                : 12
                : 4
                : e0175540
                Affiliations
                [1 ]Department of Immunoregulation and Immunodiagnostics, Chittaranjan National Cancer Institute (CNCI), Kolkata 700026, India
                [2 ]Department of Surgical Oncology and Medical Oncology, Chittaranjan National Cancer Institute (CNCI), Kolkata 700026, India
                National Institute of Allergy and Infectious Diseases, UNITED STATES
                Author notes

                Competing Interests: The authors have declared that no competing interests exist.

                • Conceptualization: MS A. Bose RB.

                • Data curation: MS SB A. Bhuniya.

                • Formal analysis: MS A. Bose RB.

                • Funding acquisition: SG A. Bose RB JB.

                • Investigation: MS SG A. Bhuniya TG IG SB.

                • Methodology: MS SG A. Bhuniya TG IG A. Bose RB.

                • Project administration: A. Bose RB.

                • Resources: RB JB.

                • Software: MS A. Bhuniya A. Bose.

                • Supervision: A. Bose RB.

                • Validation: MS A. Bhuniya A. Bose TG RB.

                • Visualization: MS SG A. Bose RB.

                • Writing – original draft: MS A. Bose RB.

                • Writing – review & editing: MS A. Bose RB.

                Article
                PONE-D-16-44570
                10.1371/journal.pone.0175540
                5393573
                28414726
                dc1ba675-4c81-4ad8-832a-aa7d881acd7b
                © 2017 Sarkar et al

                This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

                History
                : 9 November 2016
                : 24 March 2017
                Page count
                Figures: 4, Tables: 1, Pages: 16
                Funding
                Funded by: funder-id http://dx.doi.org/10.13039/501100001411, Indian Council of Medical Research;
                Award ID: 59/6/2011/BMS/TRM
                Award Recipient :
                Funded by: Department of Science and Technology
                Award ID: DST/INSPIRE FELLOWSHIP/2011/188
                Award Recipient :
                Funded by: Department of Science and Technology
                Award ID: SB/YS/LS-289/2013
                Award Recipient :
                Funded by 1. 59/6/2011/BMS/TRM, Indian Council of Medical Research, RB. 2. DST/INSPIRE FELLOWSHIP/2011/188, Department of Science and Technology, SG. 3. SB/YS/LS-289/2013, Department of Science and Technology, AB2. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
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