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dc.contributor.authorLópez Fernández, Estíbaliz
dc.contributor.authorLópez Fernández de Villaverde, José Ignacio ORCID
dc.date.accessioned2019-01-16T09:02:56Z
dc.date.available2019-01-16T09:02:56Z
dc.date.issued2018-12-04
dc.identifier.citationCancers 10 : (2018) // Article ID 485es_ES
dc.identifier.issn2072-6694
dc.identifier.urihttp://hdl.handle.net/10810/30887
dc.description.abstractMalignant tumors behave dynamically as cell communities governed by ecological principles. Massive sequencing tools are unveiling the true dimension of the heterogeneity of these communities along their evolution in most human neoplasms, clear cell renal cell carcinomas (CCRCC) included. Although initially thought to be purely stochastic processes, very recent genomic analyses have shown that temporal tumor evolution in CCRCC may follow some deterministic pathways that give rise to different clones and sub-clones randomly spatially distributed across the tumor. This fact makes each case unique, unrepeatable and unpredictable. Precise and complete molecular information is crucial for patients with cancer since it may help in establishing a personalized therapy. Intratumor heterogeneity (ITH) detection relies on the correctness of tumor sampling and this is part of the pathologist's daily work. International protocols for tumor sampling are insufficient today. They were conceived decades ago, when ITH was not an issue, and have remained unchanged until now. Noteworthy, an alternative and more efficient sampling method for detecting ITH has been developed recently. This new method, called multisite tumor sampling (MSTS), is specifically addressed to large tumors that are impossible to be totally sampled, and represent an opportunity to improve ITH detection without extra costs.es_ES
dc.description.sponsorshipThis work has been partially funded by the grant SAF2016-79847-R from Ministerio de Economía y Competitividad (MINECO), Spain (J.I.L.).es_ES
dc.language.isoenges_ES
dc.publisherMDPIes_ES
dc.relationinfo:eu-repo/grantAgreement/MINECO/SAF2016-79847-Res_ES
dc.rightsinfo:eu-repo/semantics/openAccesses_ES
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.subjectclear cell renal cell carcinomaes_ES
dc.subjecttumor evolutiones_ES
dc.subjecttumor ecologyes_ES
dc.subjectintratumor heterogeneityes_ES
dc.subjectmultisite tumor samplinges_ES
dc.subjecttargeted therapyes_ES
dc.titleThe Impact of Tumor Eco-Evolution in Renal Cell Carcinoma Samplinges_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.rights.holderThis is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited (CC BY 4.0).es_ES
dc.rights.holderAtribución 3.0 España*
dc.relation.publisherversionhttps://www.mdpi.com/2072-6694/10/12/485es_ES
dc.identifier.doi10.3390/cancers10120485
dc.departamentoesEspecialidades médico-quirúrgicases_ES
dc.departamentoeuMedikuntza eta kirurgia espezialitateakes_ES


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This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited (CC BY 4.0).
Except where otherwise noted, this item's license is described as This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited (CC BY 4.0).