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dc.creatorNikitovic, D.en
dc.creatorCorsini, E.en
dc.creatorKouretas, D.en
dc.creatorTsatsakis, A.en
dc.creatorTzanakakis, G.en
dc.date.accessioned2015-11-23T10:41:02Z
dc.date.available2015-11-23T10:41:02Z
dc.date.issued2013
dc.identifier10.1016/j.fct.2013.06.013
dc.identifier.issn0278-6915
dc.identifier.urihttp://hdl.handle.net/11615/31366
dc.description.abstractExtracellular matrices (ECMs) represent a complex network of proteins, proteoglycans and glycosaminoglycans (GAGs), composed of independent structural domains, ultimately constituting the cell microenvironment. As a highly organized, insoluble suprastructure, the ECM can, in a spatially patterned and regulated manner, integrate and deliver multiple complex signals to cells that affect their behavior. During the progression of carcinogenesis, tumor cells, through a continually changing interface, remodel and simultaneously interact with the components of ECM, as well as with surrounding stromal cells. Within this complex network of ECM components affecting tumor progression, reactive oxygen species/reactive nitrogen species (ROS/RNS) play a wide emerging role. In this minireview we will focus on the ROS-dependent modulations of tumor ECM and how this in turn affects the insidious pathways of tumor progression and dissemination. (C) 2013 Elsevier Ltd. All rights reserved.en
dc.sourceFood and Chemical Toxicologyen
dc.source.uri<Go to ISI>://WOS:000329000800027
dc.subjectTumoren
dc.subjectMetastasisen
dc.subjectExtracellular matrixen
dc.subjectROSen
dc.subjectGlycosaminoglycansen
dc.subjectMatrixen
dc.subjectmetalloproteinasesen
dc.subjectEPITHELIAL-MESENCHYMAL TRANSITIONen
dc.subjectACTIVATOR RECEPTOR EXPRESSIONen
dc.subjectBREAST-CANCER CELLSen
dc.subjectGROWTH-FACTOR-BETAen
dc.subjectREACTIVE OXYGENen
dc.subjectOXIDATIVEen
dc.subjectSTRESSen
dc.subjectNITRIC-OXIDEen
dc.subjectPLASMINOGEN-ACTIVATORen
dc.subjectFREE-RADICALSen
dc.subjectNADPHen
dc.subjectOXIDASEen
dc.subjectFood Science & Technologyen
dc.subjectToxicologyen
dc.titleROS-major mediators of extracellular matrix remodeling during tumor progressionen
dc.typejournalArticleen


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