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               <dc:title>Electrospinning Parameters Selection to Manufacture Polycaprolactone Scaffolds for Three-dimensional Breast Cancer Cell Culture and Enrichment</dc:title>
               <dc:creator>Rabionet Díaz, Marc</dc:creator>
               <dc:creator>Puig i Miquel, Teresa</dc:creator>
               <dc:creator>Ciurana, Quim de</dc:creator>
               <dc:subject>Mama -- Càncer</dc:subject>
               <dc:subject>Breast -- Cancer</dc:subject>
               <dc:subject>Materials nanoestructurats</dc:subject>
               <dc:subject>Nanostructured materials</dc:subject>
               <dc:subject>Polímers en medicina</dc:subject>
               <dc:subject>Polymers in medicine</dc:subject>
               <dc:subject>Nanotecnologia</dc:subject>
               <dc:subject>Nanotechnology</dc:subject>
               <dc:description>Only a small cell population of a breast tumour presents stem cell characteristics, thus so-called breast cancer stem cells (BCSCs). BCSCs are tumour-initiating cells and chemoresistant and they can grow in non-adherent conditions as mammospheres. Study of BCSCs is a challenge due to their low representation and the inability to propagate them without inducing differentiation. Previous studies have demonstrated that three-dimensional (3D) cell culture models such as scaffolds enhance the BCSCs population.&#xd;
&#xd;
In this project, scaffolds were fabricated by electrospinning technology. Specific values of voltage and flow rate were fixed to electrospun 7.5 and 15% poly(ɛ-caprolactone) (PCL) solutions according to process stability. Both scaffolds were seeded with MCF-7 breast cancer cells and 7.5% meshes displayed lower cell proliferation compared with 15% scaffolds. Cells cultured in both scaffolds presented a significant Mammosphere Forming Index (MFI) increase, thus indicating a BCSCs enrichment.&#xd;
&#xd;
Results show that three-dimensional cell culture with electrospun 15% PCL scaffolds could be useful to expand BCSCs population facilitating the future development of new therapeutic strategies against this tumour subpopulation</dc:description>
               <dc:description>This work was funded partially by Spanish grants from Fundación Ramón Areces, Instituto de Salud Carlos III&#xd;
(PI1400329) and by European Regional Development Fund (FEDER) and Ministerio de Economía y Competitividad&#xd;
(DPI2013-45201-P) and the support of the Catalonian government (2014SGR00868)</dc:description>
               <dc:date>2024-06-14T08:52:12Z</dc:date>
               <dc:date>2024-06-14T08:52:12Z</dc:date>
               <dc:date>2017</dc:date>
               <dc:type>info:eu-repo/semantics/article</dc:type>
               <dc:type>info:eu-repo/semantics/publishedVersion</dc:type>
               <dc:type>peer-reviewed</dc:type>
               <dc:identifier>http://hdl.handle.net/10256/15053</dc:identifier>
               <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1016/j.procir.2017.03.341</dc:relation>
               <dc:relation>info:eu-repo/semantics/altIdentifier/issn/2212-8271</dc:relation>
               <dc:relation>info:eu-repo/grantAgreement/MINECO//DPI2013-45201-P/ES/ESTUDIO Y DESARROLLO DE NUEVAS TECNOLOGIAS PARA SU APLICACION EN LA FABRICACION DE IMPLANTES/</dc:relation>
               <dc:rights>Attribution-NonCommercial-NoDerivs 4.0 Spain</dc:rights>
               <dc:rights>http://creativecommons.org/licenses/by-nc-nd/4.0/es/</dc:rights>
               <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
               <dc:publisher>Elsevier</dc:publisher>
               <dc:source>Procedia CIRP, 2017, vol. 65, p. 267-272</dc:source>
               <dc:source>Articles publicats (D-EMCI)</dc:source>
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