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Computational simulation of cellular proliferation using a meshless method

dc.contributor.authorBarbosa, M.I.A.
dc.contributor.authorBelinha, Jorge
dc.contributor.authorJorge, R.M. Natal
dc.contributor.authorCarvalho, A.X.
dc.date.accessioned2023-01-31T11:37:41Z
dc.date.embargo2035
dc.date.issued2022
dc.description.abstractBackground and objective: During cell proliferation, cells grow and divide in order to obtain two new genetically identical cells. Understanding this process is crucial to comprehend other biological processes. Computational models and algorithms have emerged to study this process and several examples can be found in the literature. The objective of this work was to develop a new computational model capable of simulating cell proliferation. This model was developed using the Radial Point Interpolation Method, a meshless method that, to the knowledge of the authors, was never used to solve this type of problem. Since the efficiency of the model strongly depends on the efficiency of the meshless method itself, the optimal numbers of integration points per integration cell and of nodes for each influence-domain were investigated. Irregular nodal meshes were also used to study their influence on the algorithm. Methods: For the first time, an iterative discrete model solved by the Radial Point Interpolation Method based on the Galerkin weak form was used to establish the system of equations from the reactiondiffusion integro-differential equations, following a new phenomenological law proposed by the authors that describes the growth of a cell over time while dependant on oxygen and glucose availability. The discretization flexibility of the meshless method allows to explicitly follow the geometric changes of the cell until the division phase. Results: It was found that an integration scheme of 6 × 6 per integration cell and influence-domains with only seven nodes allows to predict the cellular growth and division with the best balance between the relative error and the computing cost. Also, it was observed that using irregular meshes do not influence the solution. Conclusions: Even in a preliminary phase, the obtained results are promising, indicating that the algorithm might be a potential tool to study cell proliferation since it can predict cellular growth and division. Moreover, the Radial Point Interpolation Method seems to be a suitable method to study this type of process, even when irregular meshes are used. However, to optimize the algorithmpt_PT
dc.description.sponsorshipThis work was supported by Ministério da Ciência, Tecnologia e Ensino Superior - Fundação para a Ciência e a Tecnologia (Portugal) [grant number SFRH/BD/146272/2019]; and LAETA [project number UIDB/50022/2020].pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.doi10.1016/j.cmpb.2022.106974pt_PT
dc.identifier.urihttp://hdl.handle.net/10400.22/22028
dc.language.isoengpt_PT
dc.publisherElsevierpt_PT
dc.relationDevelopment of a meshless multiscale computational tool to numerically simulate MCF7 breast cancer line cell dynamics
dc.relationAssociate Laboratory of Energy, Transports and Aeronautics
dc.relation.publisherversionhttps://www.sciencedirect.com/science/article/pii/S016926072200356Xpt_PT
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/pt_PT
dc.subjectIntegration pointspt_PT
dc.subjectInfluence domainspt_PT
dc.subjectMeshless methodspt_PT
dc.subjectCell proliferationpt_PT
dc.subjectNumerical simulationpt_PT
dc.titleComputational simulation of cellular proliferation using a meshless methodpt_PT
dc.typejournal article
dspace.entity.typePublication
oaire.awardTitleDevelopment of a meshless multiscale computational tool to numerically simulate MCF7 breast cancer line cell dynamics
oaire.awardTitleAssociate Laboratory of Energy, Transports and Aeronautics
oaire.awardURIinfo:eu-repo/grantAgreement/FCT//SFRH%2FBD%2F146272%2F2019/PT
oaire.awardURIinfo:eu-repo/grantAgreement/FCT/6817 - DCRRNI ID/UIDB%2F50022%2F2020/PT
oaire.citation.startPage106974pt_PT
oaire.citation.titleComputer Methods and Programs in Biomedicinept_PT
oaire.citation.volume224pt_PT
oaire.fundingStream6817 - DCRRNI ID
person.familyNameBelinha
person.givenNameJorge
person.identifier.ciencia-id321F-ACEC-5616
person.identifier.orcid0000-0002-0539-7057
person.identifier.ridA-2118-2014
person.identifier.scopus-author-id14022409500
project.funder.identifierhttp://doi.org/10.13039/501100001871
project.funder.identifierhttp://doi.org/10.13039/501100001871
project.funder.nameFundação para a Ciência e a Tecnologia
project.funder.nameFundação para a Ciência e a Tecnologia
rcaap.rightsclosedAccesspt_PT
rcaap.typearticlept_PT
relation.isAuthorOfPublication27a63533-4e4a-46c6-b4d4-9270cc6a2371
relation.isAuthorOfPublication.latestForDiscovery27a63533-4e4a-46c6-b4d4-9270cc6a2371
relation.isProjectOfPublication03c9d70b-32fd-48cb-9aa4-9a1d76c5fcde
relation.isProjectOfPublication80741b9a-280d-4972-b352-8d1375fbfb3b
relation.isProjectOfPublication.latestForDiscovery80741b9a-280d-4972-b352-8d1375fbfb3b

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