Publication:
PanDrugs: a novel method to prioritize anticancer drug treatments according to individual genomic data

dc.contributor.authorPiñeiro-Yáñez, Elena
dc.contributor.authorReboiro-Jato, Miguel
dc.contributor.authorGomez Lopez, Gonzalo
dc.contributor.authorPerales Paton, Javier
dc.contributor.authorTroule Lozano, Kevin
dc.contributor.authorRodríguez, José Manuel
dc.contributor.authorTejero Franco, Hector
dc.contributor.authorShimamura, Takeshi
dc.contributor.authorLopez Casas, Pedro Pablo
dc.contributor.authorCarretero, Julián
dc.contributor.authorValencia, Alfonso
dc.contributor.authorHidalgo, Manuel
dc.contributor.authorGlez-Peña, Daniel
dc.contributor.authorAl-Shahrour, Fatima
dc.contributor.funderMarie Curie
dc.contributor.funderMinisterio de Economía y Competitividad (España)
dc.contributor.funderXunta de Galicia (España)
dc.contributor.funderCentro de Investigación Transferencia e Innovación -CITI
dc.contributor.funderInstituto Nacional de Bioinformatica (España)
dc.contributor.funderInstituto de Salud Carlos III
dc.date.accessioned2018-10-31T10:00:17Z
dc.date.available2018-10-31T10:00:17Z
dc.date.issued2018
dc.description.abstractBACKGROUND: Large-sequencing cancer genome projects have shown that tumors have thousands of molecular alterations and their frequency is highly heterogeneous. In such scenarios, physicians and oncologists routinely face lists of cancer genomic alterations where only a minority of them are relevant biomarkers to drive clinical decision-making. For this reason, the medical community agrees on the urgent need of methodologies to establish the relevance of tumor alterations, assisting in genomic profile interpretation, and, more importantly, to prioritize those that could be clinically actionable for cancer therapy. RESULTS: We present PanDrugs, a new computational methodology to guide the selection of personalized treatments in cancer patients using the variant lists provided by genome-wide sequencing analyses. PanDrugs offers the largest database of drug-target associations available from well-known targeted therapies to preclinical drugs. Scoring data-driven gene cancer relevance and drug feasibility PanDrugs interprets genomic alterations and provides a prioritized evidence-based list of anticancer therapies. Our tool represents the first drug prescription strategy applying a rational based on pathway context, multi-gene markers impact and information provided by functional experiments. Our approach has been systematically applied to TCGA patients and successfully validated in a cancer case study with a xenograft mouse model demonstrating its utility. CONCLUSIONS: PanDrugs is a feasible method to identify potentially druggable molecular alterations and prioritize drugs to facilitate the interpretation of genomic landscape and clinical decision-making in cancer patients. Our approach expands the search of druggable genomic alterations from the concept of cancer driver genes to the druggable pathway context extending anticancer therapeutic options beyond already known cancer genes. The methodology is public and easily integratable with custom pipelines through its programmatic API or its docker image. The PanDrugs webtool is freely accessible at http://www.pandrugs.org .es_ES
dc.description.peerreviewed
dc.description.sponsorshipThe authors thank Joaquín Dopazo, Patricia León, and José Carbonell for kindly providing the modelled pathways employed in PanDrugs implementation; and Michael Tress for his helpful comments and suggestions in the earlier version of the manuscript.es_ES
dc.format.number1es_ES
dc.format.page41es_ES
dc.format.volume10es_ES
dc.identifier.citationGenome Med. 2018; 10 (1) : 41.es_ES
dc.identifier.doi10.1186/s13073-018-0546-1es_ES
dc.identifier.e-issn1756-994Xes_ES
dc.identifier.issn1756-994Xes_ES
dc.identifier.journalGenome medicinees_ES
dc.identifier.pubmedID29848362es_ES
dc.identifier.urihttp://hdl.handle.net/20.500.12105/6554
dc.language.isoenges_ES
dc.publisherBioMed Central (BMC)
dc.relation.publisherversionhttps://doi.org/10.1186/s13073-018-0546-1es_ES
dc.repisalud.institucionCNIOes_ES
dc.repisalud.orgCNIOCNIO::Grupos de investigaciónes_ES
dc.repisalud.orgCNIOCNIO::Unidades técnicas::Unidad de Bioinformáticaes_ES
dc.rights.accessRightsopen accesses_ES
dc.rights.licenseAtribución 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subjectCancer genomicses_ES
dc.subjectDruggable genomees_ES
dc.subjectIn silico prescriptiones_ES
dc.subjectPersonalized medicinees_ES
dc.subjectPrecision oncologyes_ES
dc.subjectTargeted therapyes_ES
dc.subjectTranslational bioinformaticses_ES
dc.titlePanDrugs: a novel method to prioritize anticancer drug treatments according to individual genomic dataes_ES
dc.typejournal articlees_ES
dc.type.hasVersionVoRes_ES
dspace.entity.typePublication
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