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Vascular tumor growth and treatment: Consequences of polyclonality, competition and dynamic vascular support

dc.contributor.authorJackson, Trachette L.en_US
dc.date.accessioned2006-09-08T19:58:36Z
dc.date.available2006-09-08T19:58:36Z
dc.date.issued2002-03en_US
dc.identifier.citationJackson, Trachette L.; (2002). "Vascular tumor growth and treatment: Consequences of polyclonality, competition and dynamic vascular support." Journal of Mathematical Biology 44(3): 201-226. <http://hdl.handle.net/2027.42/42106>en_US
dc.identifier.issn0303-6812en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/42106
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=12148489&dopt=citationen_US
dc.description.abstract A mathematical model is presented to describe the evolution of a vascular tumor in response to traditional chemotherapeutic treatment. Particular attention is paid to the effects of a dynamic vascular support system in a tumor comprised of competing cell populations that differ in proliferation rates and drug susceptibility. The model consists of a system of partial differential equations governing intratumoral drug concentration, cancer cell density, and blood vessel density. The balance between cell proliferation and death along with vessel production and destruction within the tumor generates a velocity field which drives the expansion or regression of the neoplasm. Radially symmetric solutions are obtained for the case when only one cell type is present and when the proportion of the tumor occupied by blood vessels remains constant. The stability of these solutions to asymmetric perturbations and to a small semi-drug resistant cell population is then investigated. The analysis shows that drug concentrations which are sufficient to insure eradication of a spherical tumor may be inadequate for the successful treatment of non-spherical tumors. When the drug is continuously infused, linear analysis predicts that whether or not a cure is possible is crucially dependent on the proliferation rate of the semi-resistant cells and on the competitive effect of the sensitive cells on the resistant population. When the blood vessel density is allowed to change dynamically, the model predicts a dramatic increase in the tumors growth and decrease in its response to therapy.en_US
dc.format.extent522302 bytes
dc.format.extent3115 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherSpringer-Verlag; Springer-Verlag Berlin Heidelbergen_US
dc.subject.otherLegacyen_US
dc.titleVascular tumor growth and treatment: Consequences of polyclonality, competition and dynamic vascular supporten_US
dc.typeArticleen_US
dc.subject.hlbsecondlevelNatural Resources and Environmenten_US
dc.subject.hlbsecondlevelMolecular, Cellular and Developmental Biologyen_US
dc.subject.hlbsecondlevelEcology and Evolutionary Biologyen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.subject.hlbtoplevelScienceen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumUniversity of Michigan, Department of Mathematics, 525 E. University Ann Arbor, MI 48109-1109, USA. e-mail: tjacks@math.lsa.umich.edu, USen_US
dc.contributor.affiliationumcampusAnn Arboren_US
dc.identifier.pmid12148489en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/42106/1/285-44-3-201_20440201.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1007/s002850100118en_US
dc.identifier.sourceJournal of Mathematical Biologyen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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