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Modeling tumor growth and irradiation response in vitro - A combination of high-performance computing and web-based technologies including VRML visualization

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dc.contributor.author Stamatakos, GS en
dc.contributor.author Zacharaki, EI en
dc.contributor.author Makropoulou, MI en
dc.contributor.author Mouravliansky, NA en
dc.contributor.author Marsh, A en
dc.contributor.author Nikita, KS en
dc.contributor.author Uzunoglu, NK en
dc.date.accessioned 2014-03-01T01:16:46Z
dc.date.available 2014-03-01T01:16:46Z
dc.date.issued 2001 en
dc.identifier.issn 1089-7771 en
dc.identifier.uri https://dspace.lib.ntua.gr/xmlui/handle/123456789/14203
dc.subject Fractionation en
dc.subject High-performance computing en
dc.subject Modeling en
dc.subject Radiation therapy en
dc.subject Simulation en
dc.subject Tumor growth en
dc.subject Visualizalion en
dc.subject World Wide Web en
dc.subject.classification Computer Science, Information Systems en
dc.subject.classification Computer Science, Interdisciplinary Applications en
dc.subject.classification Mathematical & Computational Biology en
dc.subject.classification Medical Informatics en
dc.subject.other Tumor growth en
dc.subject.other Algorithms en
dc.subject.other Computer programming languages en
dc.subject.other Computer simulation en
dc.subject.other Irradiation en
dc.subject.other Medical computing en
dc.subject.other Monte Carlo methods en
dc.subject.other Optimization en
dc.subject.other Tumors en
dc.subject.other Virtual reality en
dc.subject.other World Wide Web en
dc.subject.other Radiotherapy en
dc.title Modeling tumor growth and irradiation response in vitro - A combination of high-performance computing and web-based technologies including VRML visualization en
heal.type journalArticle en
heal.identifier.primary 10.1109/4233.966103 en
heal.identifier.secondary http://dx.doi.org/10.1109/4233.966103 en
heal.language English en
heal.publicationDate 2001 en
heal.abstract A simplified three-dimensional Monte Carlo simulation model of in vitro tumor growth and response to fractionated radiotherapeutic schemes is presented in this paper. The paper aims at both the optimization of radiotherapy and the provision of insight into the biological mechanisms involved in tumor development. The basics of the modeling philosophy of Duechting have been adopted and substantially extended. The main processes taken into account by the model are the transitions between the cell cycle phases, the diffusion of oxygen and glucose, and the cell survival probabilities following irradiation. Specific algorithms satisfactorily describing tumor expansion and shrinkage have been applied, whereas a novel approach to the modeling of the tumor response to irradiation has been proposed and implemented. High-performance computing systems in conjunction with Web technologies have coped with the particularly high computer memory and processing demands. A visualization system based on the MATLAB software package and the virtual-reality modeling language has been employed. Its utilization has led to a spectacular representation of both the external surface and the internal structure of the developing tumor. The simulation model has been applied to the special case of small cell lung carcinoma in vitro irradiated according to both the standard and accelerated fractionation schemes. A good qualitative agreement with laboratory experience has been observed in all cases. Accordingly, the hypothesis that advanced simulation models for the in silico testing of tumor irradiation schemes could substantially enhance the radiotherapy optimization process is further strengthened. Currently, our group is investigating extensions of the presented algorithms so that efficient descriptions of the corresponding clinical (in vivo) cases are achieved. en
heal.publisher IEEE-INST ELECTRICAL ELECTRONICS ENGINEERS INC en
heal.journalName IEEE Transactions on Information Technology in Biomedicine en
dc.identifier.doi 10.1109/4233.966103 en
dc.identifier.isi ISI:000172386100003 en
dc.identifier.volume 5 en
dc.identifier.issue 4 en
dc.identifier.spage 279 en
dc.identifier.epage 289 en


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