Utilize este identificador para referenciar este registo: https://hdl.handle.net/1822/45122

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dc.contributor.authorCarvalho, Mariana R.por
dc.contributor.authorLima, Danielapor
dc.contributor.authorReis, R. L.por
dc.contributor.authorOliveira, J. M.por
dc.contributor.authorCorrelo, V. M.por
dc.date.accessioned2017-03-22T10:44:39Z-
dc.date.available2017-03-22T10:44:39Z-
dc.date.issued2017-02-
dc.date.submitted2017-
dc.identifier.issn1550-8943por
dc.identifier.urihttps://hdl.handle.net/1822/45122-
dc.description.abstractAbstract Drug toxicity frequently goes concealed until clinical trials stage, which is the most challenging, dangerous and expensive stage of drug development. Both the cultures of cancer cells in traditional 2D assays and animal studies have limitations that cannot ever be unraveled by improvements in drug-testing protocols. A new generation of bioengineered tumors is now emerging in response to these limitations, with potential to transform drug screening by providing predictive models of tumors within their tissue context, for studies of drug safety and efficacy. Considering the NCI60, a panel of 60 cancer cell lines representative of 9 different cancer types: leukemia, lung, colorectal, central nervous system (CNS), melanoma, ovarian, renal, prostate and breast, we propose to review current Bstate of art^ on the 9 cancer types specifically addressing the 3D tissue models that have been developed and used in drug discovery processes as an alternative to complement their studypor
dc.description.sponsorshipThis article is a result of the project FROnTHERA (NORTE-01-0145-FEDER-000023), supported by Norte Portugal Regional Operational Programme (NORTE 2020), under the PORTUGAL 2020 Partnership Agreement, through the European Regional Development Fund (ERDF). This article was also supported by the EU Framework Programme for Research and Innovation HORIZON 2020 (H2020) under grant agreement n° 668983 — FoReCaST. FCT distinction attributed to Joaquim M. Oliveira (IF/00423/2012) and Vitor M. Correlo (IF/01214/2014) under the Investigator FCT program is also greatly acknowledged.por
dc.language.isoengpor
dc.publisherSpringerpor
dc.relationinfo:eu-repo/grantAgreement/EC/H2020/668983/EU-
dc.rightsopenAccesspor
dc.subjectCancerpor
dc.subjectTissue engineeringpor
dc.subjectBiomaterialspor
dc.subject3Dpor
dc.subjectDrug discoverypor
dc.titleAnti-cancer drug validation: the contribution of tissue engineered modelspor
dc.typearticle-
dc.peerreviewedyespor
dc.relation.publisherversionhttps://link.springer.com/article/10.1007/s12015-017-9720-xpor
dc.commentshttp://3bs.uminho.pt/node/19012por
sdum.publicationstatuspublished-
oaire.citationStartPage1por
oaire.citationEndPage17por
oaire.citationIssue3por
oaire.citationTitleStem Cell Rev and Reppor
oaire.citationVolume13por
dc.date.updated2017-03-07T17:02:02Z-
dc.identifier.doi10.1007/s12015-017-9720-xpor
dc.identifier.pmid28233276por
dc.description.publicationversioninfo:eu-repo/semantics/publishedVersionpor
dc.subject.wosScience & Technologypor
sdum.journalStem Cell Reviews and Reportspor
Aparece nas coleções:3B’s - Artigos em revistas/Papers in scientific journals

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