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ROS-major mediators of extracellular matrix remodeling during tumor progression

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Autore
Nikitovic, D.; Corsini, E.; Kouretas, D.; Tsatsakis, A.; Tzanakakis, G.
Data
2013
DOI
10.1016/j.fct.2013.06.013
Soggetto
Tumor
Metastasis
Extracellular matrix
ROS
Glycosaminoglycans
Matrix
metalloproteinases
EPITHELIAL-MESENCHYMAL TRANSITION
ACTIVATOR RECEPTOR EXPRESSION
BREAST-CANCER CELLS
GROWTH-FACTOR-BETA
REACTIVE OXYGEN
OXIDATIVE
STRESS
NITRIC-OXIDE
PLASMINOGEN-ACTIVATOR
FREE-RADICALS
NADPH
OXIDASE
Food Science & Technology
Toxicology
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Abstract
Extracellular 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.
URI
http://hdl.handle.net/11615/31366
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