17
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Extracellular vesicles derived from cancer-associated fibroblasts induce the migration and invasion of oral squamous cell carcinoma

      research-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          ABSTRACT

          As one of the most abundant constituents of the tumour microenvironment (TME), cancer-associated fibroblasts (CAF) display critical roles during tumour progression and metastasis. Multiple classes of molecules including growth factors, cytokines, proteases and extracellular matrix proteins, are produced by CAF to act as mediators of the stroma-tumour interactions. One of the main channels for this communication is associated with extracellular vesicles (EV), which are secreted particles loaded with protein and genetic information. In this study, we evaluated the effects of EV derived from CAF primary human cell lines (n = 5) on proliferation, survival, migration, and invasion of oral squamous cell carcinoma (OSCC) cells. As controls, EV from human primary-established normal oral fibroblasts (NOF, n = 5) were used. Our in vitro assays showed that CAF-EV significantly induces migration and invasion of OSCC cells and promote a disseminated pattern of HSC-3 cell invasion in the 3D organotypic assay. Furthermore, gene expression analysis of EV-treated cancer cells revealed changes in the pathways associated with tumour metabolism and up-regulation of tumour invasion genes. Our findings suggest a significant role of CAF-EV in promoting the migration and invasion of OSCC cells, which are related to the activation of cancer-related pathways.

          Related collections

          Most cited references39

          • Record: found
          • Abstract: found
          • Article: not found

          Isolation and characterization of exosomes from cell culture supernatants and biological fluids.

          Exosomes are small membrane vesicles found in cell culture supernatants and in different biological fluids. Exosomes form in a particular population of endosomes, called multivesicular bodies (MVBs), by inward budding into the lumen of the compartment. Upon fusion of MVBs with the plasma membrane, these internal vesicles are secreted. Exosomes possess a defined set of membrane and cytosolic proteins. The physiological function of exosomes is still a matter of debate, but increasing results in various experimental systems suggest their involvement in multiple biological processes. Because both cell-culture supernatants and biological fluids contain different types of lipid membranes, it is critical to perform high-quality exosome purification. This unit describes different approaches for exosome purification from various sources, and discusses methods to evaluate the purity and homogeneity of the purified exosome preparations.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Model-based analysis of oligonucleotide arrays: expression index computation and outlier detection.

            Recent advances in cDNA and oligonucleotide DNA arrays have made it possible to measure the abundance of mRNA transcripts for many genes simultaneously. The analysis of such experiments is nontrivial because of large data size and many levels of variation introduced at different stages of the experiments. The analysis is further complicated by the large differences that may exist among different probes used to interrogate the same gene. However, an attractive feature of high-density oligonucleotide arrays such as those produced by photolithography and inkjet technology is the standardization of chip manufacturing and hybridization process. As a result, probe-specific biases, although significant, are highly reproducible and predictable, and their adverse effect can be reduced by proper modeling and analysis methods. Here, we propose a statistical model for the probe-level data, and develop model-based estimates for gene expression indexes. We also present model-based methods for identifying and handling cross-hybridizing probes and contaminating array regions. Applications of these results will be presented elsewhere.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Extracellular vesicles shuffling intercellular messages: for good or for bad.

              The release of extracellular vesicles (EVs) is a highly conserved process exploited by diverse organisms as a mode of intercellular communication. Vesicles of sizes ranging from 30 to 1000nm, or even larger, are generated by blebbing of the plasma membrane (microvesicles) or formed in multivesicular endosomes (MVEs) to be secreted by exocytosis as exosomes. Exosomes, microvesicles and other EVs contain membrane and cytosolic components that include proteins, lipids and RNAs, a composition that differs related to their site of biogenesis. Several mechanisms are involved in vesicle formation at the plasma membrane or in endosomes, which is reflected in their heterogeneity, size and composition. EVs have significant promise for therapeutics and diagnostics and for understanding physiological and pathological processes all of which have boosted research to find modulators of their composition, secretion and targeting.
                Bookmark

                Author and article information

                Journal
                J Extracell Vesicles
                J Extracell Vesicles
                ZJEV
                zjev20
                Journal of Extracellular Vesicles
                Taylor & Francis
                2001-3078
                2019
                13 February 2019
                : 8
                : 1
                : 1578525
                Affiliations
                [a ]Department of Oral Diagnosis, Piracicaba Dental School, University of Campinas , Piracicaba, Brazil
                [b ]Cancer and Translational Medicine Research Unit, Faculty of Medicine and Medical Research Center Oulu, Oulu University Hospital, University of Oulu , Oulu, Finland
                [c ]Cancer and Translational Medicine Research Unit, Biocenter Oulu and Faculty of Medicine, University of Oulu , Oulu, Finland
                [d ]Department of Pathology and Parasitology, University of Alfenas , Alfenas, Brazil
                [e ]Department of Morphology and Basic Pathology, Faculty of Medicine of Jundiai , Jundiai, Brazil
                [f ]Genomics and Expression Laboratory, Department of Genetics, Evolution and Bioagents, Institute of Biology, University of Campinas , Piracicaba, Brazil
                [g ]Brazilian Biosciences National Laboratory, LNBio, CNPEM , Campinas, Brazil
                [h ]Institute of Oral and Maxillofacial Disease, University of Helsinki, and HUSLAB, Department of Pathology, Helsinki University Hospital , Helsinki, Finland
                Author notes
                CONTACT Mauricio Rocha Dourado. mauricio_mrd@ 123456hotmail.com Department of Oral Diagnosis, School of Dentistry, University of Campinas , Piracicaba, SPCEP 13414-018, Brazil.
                [*]

                These authors contributed equally to this work.

                Author information
                http://orcid.org/0000-0002-0906-4153
                http://orcid.org/0000-0001-5285-3046
                Article
                1578525
                10.1080/20013078.2019.1578525
                6374932
                30788085
                16884c2f-5cfd-42f7-a649-2ea097a9c774
                © 2019 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group on behalf of The International Society for Extracellular Vesicles.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License ( http://creativecommons.org/licenses/by-nc/4.0/), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 27 February 2018
                : 11 December 2018
                : 18 January 2019
                Page count
                Figures: 5, References: 56, Pages: 13
                Funding
                Funded by: Coordenação de Aperfeiçoamento de Pessoal de Nível Superior - Brasil (CAPES)
                Award ID: AUXPE-PVES-570/2013
                Funded by: Coordenação de Aperfeiçoamento de Pessoal de Nível Superior - Brasil (CAPES)
                Award ID: 001
                Funded by: Finnish Cultural Foundation, Finland
                Award ID: 00130432
                Funded by: Finnish Cancer Society, Finland
                Funded by: Medical Research Center, University of Oulu, Finland
                Funded by: The Sigrid Juselius Foundation, Finland
                Funded by: Conselho Nacional de Desenvolvimento Científico e Tecnológico - CNPq, Brasília, Brazil
                Award ID: 302964/2015-0
                MRD was supported by grants from the Coordenação de Aperfeiçoamento de Pessoal de Nivel Superior - CAPES, Brasilia, Brazil [Finance Code 001] and Medical Research Center, University of Oulu, Finland. JK was supported by a grant from the Finnish Cultural Foundation [Grant number 00130432]. RDC was supported by the Coordenação de Aperfeiçoamento de Pessoal de Nivel Superior - CAPES, Brasilia, Brazil [AUXPE-PVES-570/2013]. This study was supported by the grants from the Finnish Cancer Society, The Sigrid Juselius Foundation, and the Conselho Nacional de Desenvolvimento Científico e Tecnológico - CNPq, Brasíia, Brazil [302964/2015-0].
                Categories
                Research Article

                extracellular vesicles (ev),oral cancer-associated fibroblasts (caf),migration,invasion,tumor microenvironment (tmv)

                Comments

                Comment on this article