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dc.contributor.authorCrende Arruabarrena, Olatz ORCID
dc.contributor.authorGarcía Gallastegui, Patricia ORCID
dc.contributor.authorLuzuriaga González, Jon ORCID
dc.contributor.authorBadiola Echaburu, Iker ORCID
dc.contributor.authorDe la Hoz Torres, Carmen
dc.contributor.authorUnda Rodríguez, Fernando José ORCID
dc.contributor.authorIbarretxe Bilbao, Gaskon ORCID
dc.contributor.authorPineda Martí, José Ramón ORCID
dc.date.accessioned2021-01-05T10:02:56Z
dc.date.available2021-01-05T10:02:56Z
dc.date.issued2020-11-27
dc.identifier.citationBiology 9(12) : (2020) // Article ID 426es_ES
dc.identifier.issn2079-7737
dc.identifier.urihttp://hdl.handle.net/10810/49638
dc.description.abstractThe conversion of healthy stem cells into cancer stem cells (CSCs) is believed to underlie tumor relapse after surgical removal and fuel tumor growth and invasiveness. CSCs often arise from the malignant transformation of resident multipotent stem cells, which are present in most human tissues. Some organs, such as the gut and the brain, can give rise to very aggressive types of cancers, contrary to the dental pulp, which is a tissue with a very remarkable resistance to oncogenesis. In this review, we focus on the similarities and differences between gut, brain and dental pulp stem cells and their related CSCs, placing a particular emphasis on both their shared and distinctive cell markers, including the expression of pluripotency core factors. We discuss some of their similarities and differences with regard to oncogenic signaling, telomerase activity and their intrinsic propensity to degenerate to CSCs. We also explore the characteristics of the events and mutations leading to malignant transformation in each case. Importantly, healthy dental pulp stem cells (DPSCs) share a great deal of features with many of the so far reported CSC phenotypes found in malignant neoplasms. However, there exist literally no reports about the contribution of DPSCs to malignant tumors. This raises the question about the particularities of the dental pulp and what specific barriers to malignancy might be present in the case of this tissue. These notable differences warrant further research to decipher the singular properties of DPSCs that make them resistant to transformation, and to unravel new therapeutic targets to treat deadly tumors.es_ES
dc.description.sponsorshipThis work has been financed by The University of The Basque Country (UPV/EHU): Grant number GIU16/66, UFI 11/44, COLAB19/03 and IKERTU-2020.0155 (to F.U), the Basque Government/Eusko Jaurkaritza: ELKARTEK KK-2019/00093 (to U.F.), and MINECO “Ramón y Cajal” program RYC-2013-13450 and MINECO PID2019-104766RB-C21 (to P.J.R.). L.J. was funded by a UPV/EHU postdoctoral fellowship DOKBERRI 2019 (DOCREC19/49) program.es_ES
dc.language.isoenges_ES
dc.publisherMDPIes_ES
dc.relationinfo:eu-repo/grantAgreement/MINECO/RYC-2013-13450es_ES
dc.relationinfo:eu-repo/grantAgreement/MINECO/PID2019-104766RB-C21es_ES
dc.rightsinfo:eu-repo/semantics/openAccesses_ES
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/
dc.subjectstem cellses_ES
dc.subjectcancer stem cellses_ES
dc.subjectdental pulp stem cellses_ES
dc.subjectgliomaes_ES
dc.subjectcolorectal canceres_ES
dc.subjectcell markerses_ES
dc.subjecttelomerasees_ES
dc.subjectalternative lengthening of telomereses_ES
dc.subjectpluripotency core factorses_ES
dc.titleIs There Such a Thing as a Genuine Cancer Stem Cell Marker? Perspectives from the Gut, the Brain and the Dental Pulpes_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.date.updated2020-12-24T15:54:43Z
dc.rights.holder2020 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/).es_ES
dc.relation.publisherversionhttps://www.mdpi.com/2079-7737/9/12/426/htmes_ES
dc.identifier.doi10.3390/biology9120426
dc.departamentoesBiología celular e histología
dc.departamentoeuZelulen biologia eta histologia


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2020 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/).
Except where otherwise noted, this item's license is described as 2020 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/).