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https://hdl.handle.net/10216/150431Full metadata record
| DC Field | Value | Language |
|---|---|---|
| dc.creator | Pinto, MT | |
| dc.creator | Ribeiro, AS | |
| dc.creator | Conde, I | |
| dc.creator | Carvalho, R | |
| dc.creator | Paredes, J | |
| dc.date.accessioned | 2023-06-27T13:24:24Z | - |
| dc.date.available | 2023-06-27T13:24:24Z | - |
| dc.date.issued | 2021 | |
| dc.identifier.issn | 1661-6596 | |
| dc.identifier.uri | https://hdl.handle.net/10216/150431 | - |
| dc.description.abstract | The 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.sponsorship | This 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.iso | eng | |
| dc.publisher | MDPI | |
| dc.relation | info:eu-repo/grantAgreement/FCT/6820 - DCRRNI ID/PEst-C%2FSAU%2FLA0003%2F2013/PT | |
| dc.relation | info:eu-repo/grantAgreement/FCT/9471 - RIDTI/SAICTPAC%2F0022%2F2015/PT | |
| dc.relation | info:eu-repo/grantAgreement/FCT/POR_NORTE/SFRH%2FBD%2F135831%2F2018/PT | |
| dc.relation.ispartof | International Journal of Molecular Sciences, vol.22(1):334 | |
| dc.rights | openAccess | |
| dc.rights.uri | https://creativecommons.org/licenses/by/4.0/ | |
| dc.title | The chick chorioallantoic membrane model: A new in vivo tool to evaluate breast cancer stem cell activity | |
| dc.type | Artigo em Revista Científica Internacional | |
| dc.contributor.uporto | Instituto de Investigação e Inovação em Saúde | |
| dc.identifier.doi | 10.3390/ijms22010334 | |
| dc.relation.publisherversion | https://www.mdpi.com/1422-0067/22/1/334 | |
| Appears in Collections: | I3S - Artigo em Revista Científica Internacional | |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| 10.3390-ijms22010334.pdf | 3.48 MB | Adobe PDF | ![]() View/Open |
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