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Metabolomic profiling of human lung tumor tissues - nucleotide metabolism as a candidate for therapeutic interventions and biomarkers.

dc.contributor.authorMoreno, Paula
dc.contributor.authorJimenez-Jimenez, Carla
dc.contributor.authorGarrido-Rodriguez, Martin
dc.contributor.authorCalderon-Santiago, Monica
dc.contributor.authorMolina, Susana
dc.contributor.authorLara-Chica, Maribel
dc.contributor.authorPriego-Capote, Feliciano
dc.contributor.authorSalvatierra, Angel
dc.contributor.authorMuñoz, Eduardo
dc.contributor.authorCalzado, Marco A
dc.contributor.funderConsejería de Salud (Junta de Andalucía)
dc.contributor.funderMICINN
dc.date.accessioned2023-01-25T10:21:22Z
dc.date.available2023-01-25T10:21:22Z
dc.date.issued2018-08-03
dc.description.abstractAlthough metabolomics has attracted considerable attention in the field of lung cancer (LC) detection and management, only a very limited number of works have applied it to tissues. As such, the aim of this study was the thorough analysis of metabolic profiles of relevant LC tissues, including the most important histological subtypes (adenocarcinoma and squamous cell lung carcinoma). Mass spectrometry-based metabolomics, along with genetic expression and histological analyses, were performed as part of this study, the widest to date, to identify metabolic alterations in tumors of the most relevant histological subtypes in lung. A total of 136 lung tissue samples were analyzed and 851 metabolites were identified through metabolomic analysis. Our data show the existence of a clear metabolic alteration not only between tumor vs. nonmalignant tissue in each patient, but also inherently intrinsic changes in both AC and SCC. Significant changes were observed in the most relevant biochemical pathways, and nucleotide metabolism showed an important number of metabolites with high predictive capability values. The present study provides a detailed analysis of the metabolomic changes taking place in relevant biochemical pathways of the most important histological subtypes of LC, which can be used as biomarkers and also to identify novel targets.
dc.description.sponsorshipThis work was supported by Consejería de Salud (Junta de Andalucía; PI-0650-2010 and PI-0246-2013) and MICINN (SAF2016-75228-R) grants. MLC was supported by an FPU fellowship (FPU13/03393) from Ministerio de Educación. We acknowledge Carmen Cabrero-Doncel for her assistance with the article.
dc.description.versionSi
dc.identifier.citationMoreno P, Jiménez-Jiménez C, Garrido-Rodríguez M, Calderón-Santiago M, Molina S, Lara-Chica M, et al. Metabolomic profiling of human lung tumor tissues - nucleotide metabolism as a candidate for therapeutic interventions and biomarkers. Mol Oncol. 2018 Oct;12(10):1778-1796.
dc.identifier.doi10.1002/1878-0261.12369
dc.identifier.essn1878-0261
dc.identifier.pmcPMC6165994
dc.identifier.pmid30099851
dc.identifier.pubmedURLhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6165994/pdf
dc.identifier.unpaywallURLhttps://febs.onlinelibrary.wiley.com/doi/pdfdirect/10.1002/1878-0261.12369
dc.identifier.urihttp://hdl.handle.net/10668/12825
dc.issue.number10
dc.journal.titleMolecular oncology
dc.journal.titleabbreviationMol Oncol
dc.language.isoen
dc.organizationIMIBIC
dc.page.number1778-1796
dc.provenanceRealizada la curación de contenido 03/09/2024
dc.publisherJohn Wiley & Sons Ltd.
dc.pubmedtypeJournal Article
dc.pubmedtypeResearch Support, Non-U.S. Gov't
dc.relation.projectIDPI-0650-2010
dc.relation.projectIDPI-0246-2013
dc.relation.projectIDSAF2016-75228-R
dc.relation.publisherversionhttps://onlinelibrary.wiley.com/doi/10.1002/1878-0261.12369
dc.rightsAttribution 4.0 International
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectbiomarkers
dc.subjectlung cancer
dc.subjectmetabolomics
dc.subjectnucleotides
dc.subject.decsAnciano
dc.subject.decsEstrés oxidativo
dc.subject.decsGlucosa
dc.subject.decsGlutatión
dc.subject.decsMetaboloma
dc.subject.decsMetabolómica
dc.subject.decsNucleótidos
dc.subject.decsPoliaminas
dc.subject.decsPurinas
dc.subject.decsRegulación neoplásica de la expresión génica
dc.subject.decsTransferasas de Hidroximetilo y Formilo
dc.subject.meshAged
dc.subject.meshBiomarkers, Tumor
dc.subject.meshFemale
dc.subject.meshGene Expression Regulation, Neoplastic
dc.subject.meshGlucose
dc.subject.meshGlutathione
dc.subject.meshHumans
dc.subject.meshHydroxymethyl and Formyl Transferases
dc.subject.meshLung Neoplasms
dc.subject.meshMale
dc.subject.meshMetabolome
dc.subject.meshMetabolomics
dc.subject.meshMiddle Aged
dc.subject.meshMultienzyme Complexes
dc.subject.meshNucleotide Deaminases
dc.subject.meshNucleotides
dc.subject.meshOxidative Stress
dc.subject.meshPolyamines
dc.subject.meshPurines
dc.subject.meshROC Curve
dc.titleMetabolomic profiling of human lung tumor tissues - nucleotide metabolism as a candidate for therapeutic interventions and biomarkers.
dc.typeresearch article
dc.type.hasVersionVoR
dc.volume.number12
dspace.entity.typePublication

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