Morphological Abnormalities and Gene Expression Changes Caused by High Incubation Temperatures in Zebrafish Xenografts with Human Cancer Cells

dc.contributor.affiliationUniversidade de Santiago de Compostela. Centro de Investigación en Medicina Molecular e Enfermidades Crónicasgl
dc.contributor.affiliationUniversidade de Santiago de Compostela. Departamento de Zooloxía, Xenética e Antropoloxía Físicagl
dc.contributor.authorCabezas Sáinz, Pablo
dc.contributor.authorCoppel, Carlos
dc.contributor.authorPensado López, Alba
dc.contributor.authorFernández García, Pedro
dc.contributor.authorMuinelo Romay, Laura
dc.contributor.authorLópez López, Rafael
dc.contributor.authorRubiolo Gaytán, Juan Andrés
dc.contributor.authorSánchez Piñón, Laura
dc.date.accessioned2021-02-15T13:55:08Z
dc.date.available2021-02-15T13:55:08Z
dc.date.issued2021
dc.description.abstractPublished studies show that most of the human cancer xenograft studies in zebrafish embryos have used incubation temperatures in the range of 32–34 °C for 3–6 days post-injection, trying to find a compromise temperature between the zebrafish embryos (28 °C) and the human injected cells (37 °C). While this experimental setup is widely used, a question remains: is possible to overcome the drawbacks caused by a suboptimal temperature for the injected cells? To clarify the effect of temperature and injected cells on the host, in this study, we analyzed the development and health of the last in response to different temperatures in the presence or absence of injected human cancer cells. Comparing different incubation temperatures (28, 34 and 36 °C), we determined morphological abnormalities and developmental effects in injected and non-injected embryos at different time points. Besides this, the expression of selected genes was determined by qPCR to determine temperature affected metabolic processes in the embryos. The results indicate that an incubation temperature of 36 °C during a period of 48 h is suitable for xenotransplantation without morphological or metabolic changes that could be affecting the host or the injected cells, allowing them to proliferate near their optimal temperaturegl
dc.description.peerreviewedSIgl
dc.description.sponsorshipThis research is funded by ‘Consolidación e estruturación de unidades de investigación competitivas do SUG. Grupos de referencia competitiva’ (ED431C 2018/29) and ‘Axuda á formación da etapa predoutoral’ of Xunta de Galiciagl
dc.identifier.citationGenes 2021, 12(1), 113; https://doi.org/10.3390/genes12010113gl
dc.identifier.doi10.3390/genes12010113
dc.identifier.essn2073-4425
dc.identifier.urihttp://hdl.handle.net/10347/24464
dc.language.isoenggl
dc.publisherMDPIgl
dc.relation.publisherversionhttps://doi.org/10.3390/genes12010113gl
dc.rights© 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/)gl
dc.rightsAtribución 4.0 Internacional
dc.rights.accessRightsopen accessgl
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectZebrafishgl
dc.subjectDevelopmentgl
dc.subjectXenotransplantationgl
dc.subjectIncubation-temperaturegl
dc.subjectGene-expressiongl
dc.titleMorphological Abnormalities and Gene Expression Changes Caused by High Incubation Temperatures in Zebrafish Xenografts with Human Cancer Cellsgl
dc.typejournal articlegl
dc.type.hasVersionVoRgl
dspace.entity.typePublication
relation.isAuthorOfPublicationc19125b4-8463-4fc5-bb4f-4820eb358d81
relation.isAuthorOfPublication379cc913-eaca-4c1b-a99a-6e686435238d
relation.isAuthorOfPublication6574bec8-97de-4fab-b2ba-d35b85751f34
relation.isAuthorOfPublication017b2725-d3de-40d7-8859-18c50f038d1d
relation.isAuthorOfPublication.latestForDiscoveryc19125b4-8463-4fc5-bb4f-4820eb358d81

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