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dc.contributor.authorCampbell, Kyra-
dc.contributor.authorRossi, Fabrizio-
dc.contributor.authorAdams, Jamie-
dc.contributor.authorPitsidianaki, Ioanna-
dc.contributor.authorBarriga, Francisco M.-
dc.contributor.authorGarcia-Gerique, Laura-
dc.contributor.authorBatlle, Eduard-
dc.contributor.authorCasanova, Jordi-
dc.contributor.authorCasali, Andreu-
dc.date.accessioned2020-02-20T13:46:00Z-
dc.date.available2020-02-20T13:46:00Z-
dc.date.issued2019-
dc.identifier.citationNature Communications 10: 2311 (2019)-
dc.identifier.urihttp://hdl.handle.net/10261/201412-
dc.description© The Author(s) 2019.-
dc.description.abstractMetastasis underlies the majority of cancer-related deaths yet remains poorly understood due, in part, to the lack of models in vivo. Here we show that expression of the EMT master inducer Snail in primary adult Drosophila intestinal tumors leads to the dissemination of tumor cells and formation of macrometastases. Snail drives an EMT in tumor cells, which, although retaining some epithelial markers, subsequently break through the basal lamina of the midgut, undergo a collective migration and seed polyclonal metastases. While metastases re-epithelialize over time, we found that early metastases are remarkably mesenchymal, discarding the requirement for a mesenchymal-to-epithelial transition for early stages of metastatic growth. Our results demonstrate the formation of metastases in adult flies, and identify a key role for partial-EMTs in driving it. This model opens the door to investigate the basic mechanisms underlying metastasis, in a powerful in vivo system suited for rapid genetic and drug screens.-
dc.description.sponsorshipThis study was supported by grants from the Ministerio de Economía y competitividad (Grant Numbers BFU2014–59781-P (to A.C.), BFU2015–73494-JIN (to K.C.), BFU2015–66488-P (to J.C.)). This work was also supported by the Joseph Steiner Foundation (to E.B.) and a Wellcome Trust/Royal Society Sir Henry Dale Award to K.C. (Grant number R/148777–11–1).-
dc.languageeng-
dc.publisherSpringer Nature-
dc.relationinfo:eu-repo/grantAgreement/MINECO/Plan Estatal de Investigación Científica y Técnica y de Innovación 2013-2016/BFU2014–59781-P-
dc.relationinfo:eu-repo/grantAgreement/MINECO/Plan Estatal de Investigación Científica y Técnica y de Innovación 2013-2016/BFU2015-73494-JIN-
dc.relationinfo:eu-repo/grantAgreement/MINECO/Plan Estatal de Investigación Científica y Técnica y de Innovación 2013-2016/BFU2015-66488-P-
dc.relation.isversionofPublisher's version-
dc.rightsopenAccess-
dc.subjectCancer-
dc.subjectCancer models-
dc.subjectCell biology-
dc.subjectCell migration-
dc.subjectMetastasis-
dc.titleCollective cell migration and metastases induced by an epithelial-to-mesenchymal transition in Drosophila intestinal tumors-
dc.typeartículo-
dc.identifier.doi10.1038/s41467-019-10269-y-
dc.relation.publisherversionhttp://dx.doi.org/10.1038/s41467-019-10269-y-
dc.identifier.e-issn2041-1723-
dc.date.updated2020-02-20T13:46:00Z-
dc.rights.licensehttp://creativecommons.org/licenses/by/4.0/-
dc.contributor.funderMinisterio de Economía y Competitividad (España)-
dc.contributor.funderWellcome Trust-
dc.contributor.funderRoyal Society (UK)-
dc.relation.csic-
dc.identifier.funderhttp://dx.doi.org/10.13039/501100003329es_ES
dc.identifier.funderhttp://dx.doi.org/10.13039/100004440es_ES
dc.identifier.funderhttp://dx.doi.org/10.13039/501100000288es_ES
dc.identifier.pmid31127094-
dc.type.coarhttp://purl.org/coar/resource_type/c_6501es_ES
item.openairetypeartículo-
item.grantfulltextopen-
item.cerifentitytypePublications-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextWith Fulltext-
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