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      Exosome-Based Cell-Cell Communication in the Tumor Microenvironment

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          Abstract

          Tumors are not isolated entities, but complex systemic networks involving cell-cell communication between transformed and non-transformed cells. The milieu created by tumor-associated cells may either support or halt tumor progression. In addition to cell-cell contact, cells communicate through secreted factors via a highly complex system involving characteristics such as ligand concentration, receptor expression and integration of diverse signaling pathways. Of these, extracellular vesicles, such as exosomes, are emerging as novel cell-cell communication mediators in physiological and pathological scenarios. Exosomes, membrane vesicles of endocytic origin released by all cells (both healthy and diseased), ranging in size from 30 to 150 nm, transport all the main biomolecules, including lipids, proteins, DNAs, messenger RNAs and microRNA, and perform intercellular transfer of components, locally and systemically. By acting not only in tumor cells, but also in tumor-associated cells such as fibroblasts, endothelium, leukocytes and progenitor cells, tumor- and non-tumor cells-derived exosomes have emerged as new players in tumor growth and invasion, tumor-associated angiogenesis, tissue inflammation and immunologic remodeling. In addition, due to their property of carrying molecules from their cell of origin to the peripheral circulation, exosomes have been increasingly studied as sources of tumor biomarkers in liquid biopsies. Here we review the current literature on the participation of exosomes in the communication between tumor and tumor-associated cells, highlighting the role of this process in the setup of tumor microenvironments that modulate tumor initiation and metastasis.

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          Neutrophils are indispensable antagonists of microbial infection and facilitators of wound healing. In the cancer setting, a newfound appreciation for neutrophils has come into view. The traditionally held belief that neutrophils are inert bystanders is being challenged by the recent literature. Emerging evidence indicates that tumours manipulate neutrophils, sometimes early in their differentiation process, to create diverse phenotypic and functional polarization states able to alter tumour behaviour. In this Review, we discuss the involvement of neutrophils in cancer initiation and progression, and their potential as clinical biomarkers and therapeutic targets.
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            Why don't we get more cancer? A proposed role of the microenvironment in restraining cancer progression.

            Tumors are like new organs and are made of multiple cell types and components. The tumor competes with the normal microenvironment to overcome antitumorigenic pressures. Before that battle is won, the tumor may exist within the organ unnoticed by the host, referred to as 'occult cancer'. We review how normal tissue homeostasis and architecture inhibit progression of cancer and how changes in the microenvironment can shift the balance of these signals to the procancerous state. We also include a discussion of how this information is being tailored for clinical use.
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              NK cells and cancer: you can teach innate cells new tricks.

              Natural killer (NK) cells are the prototype innate lymphoid cells endowed with potent cytolytic function that provide host defence against microbial infection and tumours. Here, we review evidence for the role of NK cells in immune surveillance against cancer and highlight new therapeutic approaches for targeting NK cells in the treatment of cancer.
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                Author and article information

                Contributors
                Journal
                Front Cell Dev Biol
                Front Cell Dev Biol
                Front. Cell Dev. Biol.
                Frontiers in Cell and Developmental Biology
                Frontiers Media S.A.
                2296-634X
                20 February 2018
                2018
                : 6
                : 18
                Affiliations
                Systems Oncology Group, Champalimaud Research, Champalimaud Foundation , Lisbon, Portugal
                Author notes

                Edited by: William Curtis Hines, University of New Mexico School of Medicine, United States

                Reviewed by: Lasse Dahl Ejby Jensen, Linköping University, Sweden; Leonard C. Edelstein, Thomas Jefferson University, United States

                *Correspondence: Bruno Costa-Silva bruno.costa-silva@ 123456research.fchampalimaud.org

                This article was submitted to Molecular Medicine, a section of the journal Frontiers in Cell and Developmental Biology

                †These authors have contributed equally to this work.

                Article
                10.3389/fcell.2018.00018
                5826063
                29515996
                51b2da6f-e5e5-49bf-8ef9-b45331212f27
                Copyright © 2018 Maia, Caja, Strano Moraes, Couto and Costa-Silva.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 06 November 2017
                : 06 February 2018
                Page count
                Figures: 2, Tables: 2, Equations: 0, References: 219, Pages: 19, Words: 16790
                Funding
                Funded by: H2020 Marie Skłodowska-Curie Actions 10.13039/100010665
                Award ID: 751547
                Categories
                Cell and Developmental Biology
                Review

                exosomes,cancer,tumor microenvironment,extracellular vesicles (evs),cell-cell communication

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