Utilize este identificador para referenciar este registo: https://hdl.handle.net/1822/51321

Registo completo
Campo DCValorIdioma
dc.contributor.authorRodrigues, Tâniapor
dc.contributor.authorKundu, Bananipor
dc.contributor.authorSilva-Correia, Joanapor
dc.contributor.authorKundu, Subhas Cpor
dc.contributor.authorOliveira, J. M.por
dc.contributor.authorReis, R. L.por
dc.contributor.authorCorrelo, V. M.por
dc.date.accessioned2018-03-01T11:41:19Z-
dc.date.available2018-03-01T11:41:19Z-
dc.date.issued2018-
dc.date.submitted2017-
dc.identifier.citationRodrigues T., Kundu B., Silva-Correia J., Kundu S. C., Oliveira J. M., Reis R. L., Correlo V. M. Emerging tumor spheroids technologies for 3D in vitro cancer modeling, Pharmacology & Therapeutics, doi:10.1016/j.pharmthera.2017.10.018, 2018.por
dc.identifier.issn0163-7258por
dc.identifier.urihttps://hdl.handle.net/1822/51321-
dc.description"Article in Press, Available online 31 October 2017" ; "S0163-7258(17)30268-1"por
dc.description.abstractCancer is a leading cause of mortality and morbidity worldwide. Around 90% of deaths are caused by metastasis and just 10% by primary tumor. The advancement of treatment approaches is not at the same rhythm of the disease; making cancer a focal target of biomedical research. To enhance the understanding and promts the therapeutic delivery; concepts of tissue engineering are applied in the development of in vitro models that can bridge between 2D cell culture and animal models, mimicking tissue microenvironment. Tumor spheroid represents highly suitable 3D organoid-like framework elucidiating the intra and inter cellular signaling of cancer, like that formed in physiological niche. However, spheroids are of limited value in studying critical biological phenomenon such as tumor-stroma interactons involving extra cellular matrix or immune system. Therefore, a compelling need of tailoring spheroid technologies with physiologically relevant biomaterials or in silico models, is ever emerging. The diagnostic and prognostic role of spheroids rearrangements within biomaterials or microfluidic channel is indicative of patient management; particularly for the decision of targated therapy. Fragmented information on available in vitro spheroid models and lack of critical analysis on transformation aspects of these strategies; pushes the urge to comprehensively overview the recent technological advancements (e.g. bioprinting, micro-fluidic technologies or use of biomaterials to attain the third dimension) in the shed of tranlationable cancer research. In present article, relationships between current models and their possible exploitation in clinical success is explored with the highlight of existing challenges in defining therapeutic targets and screening of drug efficacy.por
dc.description.sponsorshipThe authors are thankful to European Union (Horizon 2020) funded project FoReCaST (No. 668983), the FCT fellowship to J. Silva-Correia (Grant No. SFRH/BPD/100590/2014), distinctions to J.M.O. under the Investigator FCT program (IF/00423/2012) and V.M.C. under the Investigator FCT program (IF/01214/2014) for supporting this work financially.por
dc.language.isoengpor
dc.publisherElsevier 1por
dc.relationinfo:eu-repo/grantAgreement/EC/H2020/668983/EU-
dc.relationinfo:eu-repo/grantAgreement/FCT/FARH/SFRH%2FBPD%2F100590%2F2014/PT-
dc.relationinfo:eu-repo/grantAgreement/FCT/Investigador FCT/IF%2F00423%2F2012%2FCP0177%2FCT0004/PT-
dc.relationinfo:eu-repo/grantAgreement/FCT/Investigador FCT/IF%2F01214%2F2014%2FCP1212%2FCT0014/PT-
dc.rightsopenAccesspor
dc.subjectMetastasispor
dc.subject3D Tumor Modelspor
dc.subjectMulticellular Tumor Spheroidspor
dc.subjectBioprintingpor
dc.subjectBiomaterialspor
dc.titleEmerging tumor spheroids technologies for 3D in vitro cancer modelingpor
dc.typearticle-
dc.peerreviewedyespor
dc.relation.publisherversionhttps://doi.org/10.1016/j.pharmthera.2017.10.018por
dc.commentshttp://3bs.uminho.pt/node/19251por
oaire.citationStartPage201por
oaire.citationEndPage211por
oaire.citationVolume184por
dc.date.updated2018-02-09T17:16:41Z-
dc.identifier.eissn1879-016Xpor
dc.identifier.doi10.1016/j.pharmthera.2017.10.018por
dc.identifier.pmid29097309por
dc.description.publicationversioninfo:eu-repo/semantics/publishedVersionpor
dc.subject.wosScience & Technologypor
sdum.journalPharmacology and Therapeuticspor
Aparece nas coleções:3B’s - Artigos em revistas/Papers in scientific journals

Ficheiros deste registo:
Ficheiro Descrição TamanhoFormato 
19251-T. Rodrigues et al.pdf739,5 kBAdobe PDFVer/Abrir

Partilhe no FacebookPartilhe no TwitterPartilhe no DeliciousPartilhe no LinkedInPartilhe no DiggAdicionar ao Google BookmarksPartilhe no MySpacePartilhe no Orkut
Exporte no formato BibTex mendeley Exporte no formato Endnote Adicione ao seu ORCID