Please use this identifier to cite or link to this item: https://hdl.handle.net/10316/95681
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dc.contributor.authorCarvalho, João-
dc.date.accessioned2021-08-26T16:14:42Z-
dc.date.available2021-08-26T16:14:42Z-
dc.date.issued2021-06-30-
dc.identifier.issn2045-2322-
dc.identifier.urihttps://hdl.handle.net/10316/95681-
dc.description.abstractAs the main theory of carcinogenesis, the Somatic Mutation Theory, increasingly presents difficulties to explain some experimental observations, different theories are being proposed. A major alternative approach is the Tissue Organization Field Theory, which explains cancer origin as a tissue regulation disease instead of having a mainly cellular origin. This work fits in the latter hypothesis, proposing the bioelectric field, in particular the cell membrane polarization state, and ionic exchange through ion channels and gap junctions, as an important mechanism of cell communication and tissue organization and regulation. Taking into account recent experimental results and proposed bioelectric models, a computational model of cancer initiation was developed, including the propagation of a cell depolarization wave in the tissue under consideration. Cell depolarization leads to a change in its state, with the activation and deactivation of several regulation pathways, increasing cell proliferation and motility, changing its epigenetic state to a more stem cell-like behavior without the requirement of genomic mutation. The intercellular communication via gap junctions leads, in certain circumstances, to a bioelectric state propagation to neighbor cells, in a chain-like reaction, till an electric discontinuity is reached. However, this is a reversible process, and it was shown experimentally that, by implementing a therapy targeted on cell ion exchange channels, it is possible to reverse the state and repolarize cells. This mechanism can be an important alternative way in cancer prevention, diagnosis and therapy, and new experiments are proposed to test the presented hypothesis.pt
dc.language.isoengpt
dc.publisherSpringer Naturept
dc.relationUIDB/04564/2020pt
dc.relationUIDP/04564/2020pt
dc.rightsopenAccesspt
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/pt
dc.titleA bioelectric model of carcinogenesis, including propagation of cell membrane depolarization and reversal therapiespt
dc.typearticlept
degois.publication.firstPage13607pt
degois.publication.issue1pt
degois.publication.titleScientific Reportspt
dc.peerreviewedyespt
dc.identifier.doi34193902-
dc.identifier.doi2045-2322-
dc.identifier.doi2045-2322-
dc.identifier.doi34193902-
dc.identifier.doi10.1038/s41598-021-92951-0-
dc.identifier.doi34193902-
dc.identifier.doi2045-2322-
degois.publication.volume11pt
dc.date.embargo2021-06-30*
dc.identifier.pmid34193902-
uc.date.periodoEmbargo0pt
dc.identifier.eissn2045-2322-
item.grantfulltextopen-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextCom Texto completo-
item.openairetypearticle-
item.cerifentitytypePublications-
item.languageiso639-1en-
crisitem.author.researchunitCFisUC – Center for Physics of the University of Coimbra-
crisitem.author.orcid0000-0002-3015-7821-
crisitem.project.grantnoCenter for Physics of the University of Coimbra-
crisitem.project.grantnoCenter for Physics of the University of Coimbra-
Appears in Collections:I&D CFis - Artigos em Revistas Internacionais
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