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dc.contributor.authorStylianopoulos, T.en
dc.creatorStylianopoulos, T.en
dc.date.accessioned2019-05-06T12:24:39Z
dc.date.available2019-05-06T12:24:39Z
dc.date.issued2017
dc.identifier.urihttp://gnosis.library.ucy.ac.cy/handle/7/48847
dc.description.abstractTumor progression and response to treatment is determined in large part by the generation of mechanical stresses that stem from both the solid and the fluid phase of the tumor. Furthermore, elevated solid stress levels can regulate fluid stresses by compressing intratumoral blood and lymphatic vessels. Blood vessel compression reduces tumor perfusion, while compression of lymphatic vessels hinders the ability of the tumor to drain excessive fluid from its interstitial space contributing to the uniform elevation of the interstitial fluid pressure. Hypoperfusion and interstitial hypertension pose major barriers to the systemic administration of chemotherapeutic agents and nanomedicines to tumors, reducing treatment efficacies. Hypoperfusion can also create a hypoxic and acidic tumor microenvironment that promotes tumor progression and metastasis. Hence, alleviation of intratumoral solid stress levels can decompress tumor vessels and restore perfusion and interstitial fluid pressure. In this review, three major types of tissue level solid stresses involved in tumor growth, namely stress exerted externally on the tumor by the host tissue, swelling stress, and residual stress, are discussed separately and details are provided regarding their causes, magnitudes, and remedies. Subsequently, evidence of how stress-alleviating drugs could be used in combination with chemotherapy to improve treatment efficacy is presented, highlighting the potential of stress-alleviation strategies to enhance cancer therapy. Finally, a continuum-level, mathematical framework to incorporate these types of solid stress is outlined. Copyright © 2017 by ASME.en
dc.language.isoengen
dc.sourceJournal of Biomechanical Engineeringen
dc.subjectMathematical modelsen
dc.subjectModelsen
dc.subjecttheoretical modelen
dc.subjectmathematical modelen
dc.subjectantineoplastic agenten
dc.subjectAntineoplastic Agentsen
dc.subjecthumanen
dc.subjectNeoplasmsen
dc.subjectHumansen
dc.subjecttreatment outcomeen
dc.subjecttumor microenvironmenten
dc.subjectneoplasmen
dc.subjectbiological modelen
dc.subjectcell proliferationen
dc.subjectnonhumanen
dc.subjectpathologyen
dc.subjectStressen
dc.subjecttumor growthen
dc.subjectcancer therapyen
dc.subjectArticleen
dc.subjectBiologicalen
dc.subjectchemotherapyen
dc.subjectpathophysiologyen
dc.subjectcancer cellen
dc.subjectAnimalsen
dc.subjectanimalen
dc.subjecthypoxiaen
dc.subjectNeovascularizationen
dc.subjectneovascularization (pathology)en
dc.subjectPathologicen
dc.subjectswellingen
dc.subjectdrug effectsen
dc.subjectdrug delivery systemen
dc.subjectcomputer simulationen
dc.subjectMathematical frameworksen
dc.subjectStressesen
dc.subjectmathematical modelingen
dc.subjectTumorsen
dc.subjectInterstitial fluid pressuresen
dc.subjectTissueen
dc.subjectDiseasesen
dc.subjecttissue pressureen
dc.subjectTumor progressionsen
dc.subjectperfusionen
dc.subjectMechanicalen
dc.subjectBlood vesselsen
dc.subjectangiogenesis inhibitoren
dc.subjectAngiogenesis Inhibitorsen
dc.subjectYoung modulusen
dc.subjectmechanical stressen
dc.subjectsolid stressen
dc.subjectbiomechanicsen
dc.subjectChemotherapeutic agentsen
dc.subjectcompressive strengthen
dc.subjectdrug deliveryen
dc.subjectElastic Modulusen
dc.subjectmalignant neoplasmen
dc.subjectSystemic administrationen
dc.subjecttensile strengthen
dc.subjecttumor modelen
dc.titleThe Solid Mechanics of Cancer and Strategies for Improved Therapyen
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1115/1.4034991
dc.description.volume139
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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