Publication:
Gene Expression Integration into Pathway Modules Reveals a Pan-Cancer Metabolic Landscape.

dc.contributor.authorCubuk, Cankut
dc.contributor.authorHidalgo, Marta R
dc.contributor.authorAmadoz, Alicia
dc.contributor.authorPujana, Miguel A
dc.contributor.authorMateo, Francesca
dc.contributor.authorHerranz, Carmen
dc.contributor.authorCarbonell-Caballero, Jose
dc.contributor.authorDopazo, Joaquin
dc.date.accessioned2023-01-25T10:21:37Z
dc.date.available2023-01-25T10:21:37Z
dc.date.issued2018-08-22
dc.description.abstractMetabolic reprogramming plays an important role in cancer development and progression and is a well-established hallmark of cancer. Despite its inherent complexity, cellular metabolism can be decomposed into functional modules that represent fundamental metabolic processes. Here, we performed a pan-cancer study involving 9,428 samples from 25 cancer types to reveal metabolic modules whose individual or coordinated activity predict cancer type and outcome, in turn highlighting novel therapeutic opportunities. Integration of gene expression levels into metabolic modules suggests that the activity of specific modules differs between cancers and the corresponding tissues of origin. Some modules may cooperate, as indicated by the positive correlation of their activity across a range of tumors. The activity of many metabolic modules was significantly associated with prognosis at a stronger magnitude than any of their constituent genes. Thus, modules may be classified as tumor suppressors and oncomodules according to their potential impact on cancer progression. Using this modeling framework, we also propose novel potential therapeutic targets that constitute alternative ways of treating cancer by inhibiting their reprogrammed metabolism. Collectively, this study provides an extensive resource of predicted cancer metabolic profiles and dependencies.Significance: Combining gene expression with metabolic modules identifies molecular mechanisms of cancer undetected on an individual gene level and allows discovery of new potential therapeutic targets. Cancer Res; 78(21); 6059-72. ©2018 AACR.
dc.identifier.doi10.1158/0008-5472.CAN-17-2705
dc.identifier.essn1538-7445
dc.identifier.pmid30135189
dc.identifier.unpaywallURLhttps://qmro.qmul.ac.uk/xmlui/bitstream/123456789/56651/5/Cubuk_Gene%20expression%20integration_2018_Accepted.pdf
dc.identifier.urihttp://hdl.handle.net/10668/12866
dc.issue.number21
dc.journal.titleCancer research
dc.journal.titleabbreviationCancer Res
dc.language.isoen
dc.organizationHospital Universitario Virgen del Rocío
dc.page.number6059-6072
dc.pubmedtypeJournal Article
dc.pubmedtypeResearch Support, Non-U.S. Gov't
dc.rights.accessRightsopen access
dc.subject.meshCell Line, Tumor
dc.subject.meshCluster Analysis
dc.subject.meshDisease Progression
dc.subject.meshGene Expression Profiling
dc.subject.meshGene Expression Regulation, Neoplastic
dc.subject.meshGene Regulatory Networks
dc.subject.meshHumans
dc.subject.meshKaplan-Meier Estimate
dc.subject.meshMetabolome
dc.subject.meshMutation
dc.subject.meshNeoplasms
dc.subject.meshOncogenes
dc.subject.meshPhenotype
dc.subject.meshPrognosis
dc.subject.meshRNA, Small Interfering
dc.subject.meshSequence Analysis, RNA
dc.subject.meshTranscriptome
dc.subject.meshTreatment Outcome
dc.titleGene Expression Integration into Pathway Modules Reveals a Pan-Cancer Metabolic Landscape.
dc.typeresearch article
dc.type.hasVersionVoR
dc.volume.number78
dspace.entity.typePublication

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