dc.creatorBelgorosky, Denise
dc.creatorFernández Cabada, Tamara
dc.creatorPeñaherrera Pazmiño, Ana Belén
dc.creatorLangle, Yanina Verónica
dc.creatorBooth, Ross
dc.creatorBhansali, Shekhar
dc.creatorPerez, Maximiliano Sebastian
dc.creatorEijan, Ana Maria
dc.creatorLerner, Betiana
dc.date.accessioned2020-11-04T13:42:26Z
dc.date.accessioned2022-10-15T05:27:10Z
dc.date.available2020-11-04T13:42:26Z
dc.date.available2022-10-15T05:27:10Z
dc.date.created2020-11-04T13:42:26Z
dc.date.issued2018-09
dc.identifierBelgorosky, Denise; Fernández Cabada, Tamara; Peñaherrera Pazmiño, Ana Belén; Langle, Yanina Verónica; Booth, Ross; et al.; Analysis of tumoral spheres growing in a multichamber microfluidic device; Veterinary and Human Toxicology; Journal of Cellular Physiology; 233; 9; 9-2018; 6327-6336
dc.identifier0021-9541
dc.identifierhttp://hdl.handle.net/11336/117585
dc.identifierCONICET Digital
dc.identifierCONICET
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/4349655
dc.description.abstractLab on a Chip (LOC) farming systems have emerged as a powerful tool for single cell studies combined with a non‐adherent cell culture substrate and single cell capture chips for the study of single cell derived tumor spheres. Cancer is characterized by its cellular heterogeneity where only a small population of cancer stem cells (CSCs) are responsible for tumor metastases and recurrences. Thus, the in vitro strategy to the formation of a single cell‐derived sphere is an attractive alternative to identify CSCs. In this study, we test the effectiveness of microdevices for analysis of heterogeneity within CSC populations and its interaction with different components of the extracellular matrix. CSC could be identify using specific markers related to its pluripotency and self‐renewal characteristics such as the transcription factor Oct‐4 or the surface protein CD44. The results confirm the usefulness of LOC as an effective method for quantification of CSC, through the formation of spheres under conditions of low adhesion or growing on components of the extracellular matrix. The device used is also a good alternative for evaluating the individual growth of each sphere and further identification of these CSC markers by immunofluorescence. In conclusion, LOC devices have not only the already known advantages, but they are also a promising tool since they use small amounts of reagents and are under specific culture parameters. LOC devices could be considered as a novel technology to be used as a complement or replacement of traditional studies on culture plates.
dc.languageeng
dc.publisherVeterinary and Human Toxicology
dc.relationinfo:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1002/jcp.26519
dc.relationinfo:eu-repo/semantics/altIdentifier/url/https://onlinelibrary.wiley.com/doi/abs/10.1002/jcp.26519
dc.rightshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.rightsinfo:eu-repo/semantics/restrictedAccess
dc.subjectLAB ON A CHIP
dc.subjectCANCER STEM CELL
dc.subjectSPHERE FORMATION ASSAY
dc.subjectTUMORAL SPHERE
dc.titleAnalysis of tumoral spheres growing in a multichamber microfluidic device
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:ar-repo/semantics/artículo
dc.typeinfo:eu-repo/semantics/publishedVersion


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