Utilize este identificador para referenciar este registo: https://hdl.handle.net/10216/150431
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Campo DCValorIdioma
dc.creatorPinto, MT
dc.creatorRibeiro, AS
dc.creatorConde, I
dc.creatorCarvalho, R
dc.creatorParedes, J
dc.date.accessioned2023-06-27T13:24:24Z-
dc.date.available2023-06-27T13:24:24Z-
dc.date.issued2021
dc.identifier.issn1661-6596
dc.identifier.urihttps://hdl.handle.net/10216/150431-
dc.description.abstractThe high plasticity of cancer stem-like cells (CSCs) allows them to differentiate and proliferate, specifically when xenotransplanted subcutaneously into immunocompromised mice. CSCs are highly tumorigenic, even when inoculated in small numbers. Thus, in vivo limiting dilution assays (LDA) in mice are the current gold standard method to evaluate CSC enrichment and activity. The chick embryo chorioallantoic membrane (CAM) is a low cost, naturally immuneincompetent and reproducible model widely used to evaluate the spontaneous growth of human tumor cells. Here, we established a CAM-LDA assay able to rapidly reproduce tumor specificities— in particular, the ability of the small population of CSCs to form tumors. We used a panel of organotropic metastatic breast cancer cells, which show an enrichment in a stem cell gene signature, enhanced CD44+/CD24-/low cell surface expression and increased mammosphere-forming efficiency (MFE). The size of CAM-xenografted tumors correlate with the number of inoculated cancer cells, following mice xenograft growth pattern. CAM and mice tumors are histologically comparable, displaying both breast CSC markers CD44 and CD49f. Therefore, we propose a new tool for studying CSC prevalence and function—the chick CAM-LDA—a model with easy handling, accessibility, rapid growth and the absence of ethical and regulatory constraints.
dc.description.sponsorshipThis work was funded by FEDER—Fundo Europeu de Desenvolvimento Regional— funds through the COMPETE 2020—Operacional Programme for Competitiveness and Internationalisation (POCI), Portugal 2020, and by FCT—Fundação para a Ciência e a Tecnologia/Ministério da Ciência, Tecnologia e Ensino Superior under the projects PestC/SAU/LA0003/2013, NORTE-01-0145-FEDER-000029, SAICTPAC/0022/2015 and FCT/02/SAICT/2017/030625. FCT funded the research grant of RC (SFRH/BD/135831/2018). IPATIMUP integrated the i3S Research Unit, which was partially supported by FCT in the framework of the project “Institute for Research and Innovation in Health Sciences” (POCI-01-0145FEDER-007274).
dc.language.isoeng
dc.publisherMDPI
dc.relationinfo:eu-repo/grantAgreement/FCT/6820 - DCRRNI ID/PEst-C%2FSAU%2FLA0003%2F2013/PT
dc.relationinfo:eu-repo/grantAgreement/FCT/9471 - RIDTI/SAICTPAC%2F0022%2F2015/PT
dc.relationinfo:eu-repo/grantAgreement/FCT/POR_NORTE/SFRH%2FBD%2F135831%2F2018/PT
dc.relation.ispartofInternational Journal of Molecular Sciences, vol.22(1):334
dc.rightsopenAccess
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.titleThe chick chorioallantoic membrane model: A new in vivo tool to evaluate breast cancer stem cell activity
dc.typeArtigo em Revista Científica Internacional
dc.contributor.uportoInstituto de Investigação e Inovação em Saúde
dc.identifier.doi10.3390/ijms22010334
dc.relation.publisherversionhttps://www.mdpi.com/1422-0067/22/1/334
Aparece nas coleções:I3S - Artigo em Revista Científica Internacional

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