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dc.contributor.authorVoutouri, C.en
dc.contributor.authorMpekris, F.en
dc.contributor.authorPapageorgis, P.en
dc.contributor.authorOdysseos, A. D.en
dc.contributor.authorStylianopoulos, T.en
dc.creatorVoutouri, C.en
dc.creatorMpekris, F.en
dc.creatorPapageorgis, P.en
dc.creatorOdysseos, A. D.en
dc.creatorStylianopoulos, T.en
dc.date.accessioned2019-05-06T12:24:48Z
dc.date.available2019-05-06T12:24:48Z
dc.date.issued2014
dc.identifier.urihttp://gnosis.library.ucy.ac.cy/handle/7/48928
dc.description.abstractMechanical forces play a crucial role in tumor patho-physiology. Compression of cancer cells inhibits their proliferation rate, induces apoptosis and enhances their invasive and metastatic potential. Additionally, compression of intratumor blood vessels reduces the supply of oxygen, nutrients and drugs, affecting tumor progression and treatment. Despite the great importance of the mechanical microenvironment to the pathology of cancer, there are limited studies for the constitutive modeling and the mechanical properties of tumors and on how these parameters affect tumor growth. Also, the contribution of the host tissue to the growth and state of stress of the tumor remains unclear. To this end, we performed unconfined compression experiments in two tumor types and found that the experimental stress-strain response is better fitted to an exponential constitutive equation compared to the widely used neo-Hookean and Blatz-Ko models. Subsequently, we incorporated the constitutive equations along with the corresponding values of the mechanical properties - calculated by the fit - to a biomechanical model of tumor growth. Interestingly, we found that the evolution of stress and the growth rate of the tumor are independent from the selection of the constitutive equation, but depend strongly on the mechanical interactions with the surrounding host tissue. Particularly, model predictions - in agreement with experimental studies - suggest that the stiffness of solid tumors should exceed a critical value compared with that of the surrounding tissue in order to be able to displace the tissue and grow in size. With the use of the model, we estimated this critical value to be on the order of 1.5. Our results suggest that the direct effect of solid stress on tumor growth involves not only the inhibitory effect of stress on cancer cell proliferation and the induction of apoptosis, but also the resistance of the surrounding tissue to tumor expansion. © 2014 Voutouri et al.en
dc.language.isoengen
dc.sourcePLoS ONEen
dc.subjectModelsen
dc.subjectarticleen
dc.subjectmathematical modelen
dc.subjecthumanen
dc.subjectHumansen
dc.subjectBreast Neoplasmsen
dc.subjectcontrolled studyen
dc.subjectfemaleen
dc.subjectDisease Progressionen
dc.subjecttumor microenvironmenten
dc.subjectsolid tumoren
dc.subjectdisease courseen
dc.subjectbiological modelen
dc.subjectcell proliferationen
dc.subjectnonhumanen
dc.subjectpathologyen
dc.subjectStressen
dc.subjecttumor growthen
dc.subjectBiologicalen
dc.subjectpathophysiologyen
dc.subjectcancer cellen
dc.subjecthuman cellen
dc.subjectapoptosisen
dc.subjectanimal experimenten
dc.subjectanimal modelen
dc.subjectanimal tissueen
dc.subjectmouseen
dc.subjectColonic Neoplasmsen
dc.subjectnonlinear systemen
dc.subjectTumoren
dc.subjectbreast tumoren
dc.subjectCell Lineen
dc.subjectBiomechanical Phenomenaen
dc.subjectMechanicalen
dc.subjectYoung modulusen
dc.subjectmechanical stressen
dc.subjectcell stressen
dc.subjecttumor cell lineen
dc.subjectbiomechanicsen
dc.subjectmaterials testingen
dc.subjectgrowth rateen
dc.subjectcolon tumoren
dc.subjectNonlinear Dynamicsen
dc.subjectviscoelasticityen
dc.titleRole of constitutive behavior and tumor-host mechanical interactions in the state of stress and growth of solid tumorsen
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1371/journal.pone.0104717
dc.description.volume9
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.gnosis.orcid0000-0002-3093-1696


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