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dc.contributor.authorPirentis, A. P.en
dc.contributor.authorPolydorou, C.en
dc.contributor.authorPapageorgis, P.en
dc.contributor.authorVoutouri, C.en
dc.contributor.authorMpekris, F.en
dc.contributor.authorStylianopoulos, T.en
dc.creatorPirentis, A. P.en
dc.creatorPolydorou, C.en
dc.creatorPapageorgis, P.en
dc.creatorVoutouri, C.en
dc.creatorMpekris, F.en
dc.creatorStylianopoulos, T.en
dc.date.accessioned2019-05-06T12:24:21Z
dc.date.available2019-05-06T12:24:21Z
dc.date.issued2015
dc.identifier.urihttp://gnosis.library.ucy.ac.cy/handle/7/48724
dc.description.abstractSolid stresses emerge as the expanding tumor displaces and deforms the surrounding normal tissue, and also as a result of intratumoral component interplay. Among other things, solid stresses are known to induce extensive extracellular matrix synthesis and reorganization. In this study, we developed a mathematical model of tumor growth that distinguishes the contribution to stress generation by collagenous and non-collagenous tumor structural components, and also investigates collagen fiber remodeling exclusively due to solid stress. To this end, we initially conducted in vivo experiments using an orthotopic mouse model for breast cancer to monitor primary tumor growth and derive the mechanical properties of the tumor. Subsequently, we fitted the mathematical model to experimental data to determine values of the model parameters. According to the model, intratumoral solid stress is compressive, whereas extratumoral stress in the tumor vicinity is compressive in the radial direction and tensile in the periphery. Furthermore, collagen fibers engaged in stress generation only in the peritumoral region, and not in the interior where they were slackened due to the compressive stress state. Peritumoral fibers were driven away from the radial direction, tended to realign tangent to the tumor-host interface, and were also significantly stretched by tensile circumferential stresses. By means of this remodeling, the model predicts that the tumor is enveloped by a progressively thickening capsule of collagen fibers. This prediction is consistent with long-standing observations of tumor encapsulation and histologic sections that we performed, and it further corroborates the expansive growth hypothesis for the capsule formation. © 2015 © 2015 Taylor & Francis Group, LLC.en
dc.language.isoengen
dc.sourceConnective tissue researchen
dc.subjectModelsen
dc.subjecttheoretical modelen
dc.subjectmathematical modelen
dc.subjectTheoreticalen
dc.subjecthumanen
dc.subjectbreast canceren
dc.subjectBreast Neoplasmsen
dc.subjectcontrolled studyen
dc.subjectfemaleen
dc.subjecttumor microenvironmenten
dc.subjecttissue sectionen
dc.subjectnonhumanen
dc.subjectpathologyen
dc.subjectStressen
dc.subjecttumor growthen
dc.subjectArticleen
dc.subjectmetabolismen
dc.subjecthuman cellen
dc.subjectAnimalsen
dc.subjectMiceen
dc.subjectanimalen
dc.subjectAnimalen
dc.subjectanimal cellen
dc.subjectanimal experimenten
dc.subjectanimal modelen
dc.subjectanimal tissueen
dc.subjectdisease modelen
dc.subjectDisease Modelsen
dc.subjectmouseen
dc.subjectphysiologyen
dc.subjectprimary tumoren
dc.subjectstressen
dc.subjectTumoren
dc.subjectbreast tumoren
dc.subjectCell Lineen
dc.subjectcollagenen
dc.subjectmathematical modelingen
dc.subjectBiomechanical Phenomenaen
dc.subjectextracellular matrixen
dc.subjectMechanicalen
dc.subjectkinematicsen
dc.subjectmechanical stressen
dc.subjecttumor cell lineen
dc.subjectbiomechanicsen
dc.subjectcollagen fiberen
dc.subjectCollagen fiber remodelingen
dc.subjectencapsulationen
dc.subjectexpansive growth hypothesisen
dc.subjecttumor encapsulationen
dc.subjecttumor mechanicsen
dc.titleRemodeling of extracellular matrix due to solid stress accumulation during tumor growthen
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.3109/03008207.2015.1047929
dc.description.volume56
dc.description.startingpage345
dc.description.endingpage354
dc.author.facultyΠολυτεχνική Σχολή / Faculty of Engineering
dc.author.departmentΤμήμα Μηχανικών Μηχανολογίας και Κατασκευαστικής / Department of Mechanical and Manufacturing Engineering
dc.type.uhtypeArticleen
dc.contributor.orcidStylianopoulos, T. [0000-0002-3093-1696]
dc.description.totalnumpages345-354
dc.gnosis.orcid0000-0002-3093-1696


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