Please use this identifier to cite or link to this item: https://hdl.handle.net/10316/103554
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dc.contributor.authorFonseca, André-
dc.contributor.authorRamalhete, Sara Ventura-
dc.contributor.authorMestre, André-
dc.contributor.authorNeves, Ricardo Pires das-
dc.contributor.authorMarreiros, Ana-
dc.contributor.authorCastelo Branco, Pedro-
dc.contributor.authorRoberto, Vânia Palma-
dc.date.accessioned2022-11-18T11:39:39Z-
dc.date.available2022-11-18T11:39:39Z-
dc.date.issued2021-
dc.identifier.issn1945-4589pt
dc.identifier.urihttps://hdl.handle.net/10316/103554-
dc.description.abstractColorectal cancer is one of the leading causes of cancer-related deaths worldwide. This complex disease still holds severe problems concerning diagnosis due to the high invasiveness nature of colonoscopy and the low accuracy of the alternative diagnostic methods. Additionally, patient heterogeneity even within the same stage is not properly reflected in the current stratification system. This scenario highlights the need for new biomarkers to improve non-invasive screenings and clinical management of patients. MicroRNAs (miRNAs) have emerged as good candidate biomarkers in cancer as they are stable molecules, easily measurable and detected in body fluids thus allowing for non-invasive diagnosis and/or prognosis. In this study, we performed an integrated analysis first using 4 different datasets (discovery cohorts) to identify miRNAs associated with colorectal cancer development, unveil their role in this disease by identifying putative targets and regulatory networks and investigate their ability to serve as biomarkers. We have identified 26 differentially expressed miRNAs which interact with frequently deregulated genes known to participate in commonly altered pathways in colorectal cancer. Most of these miRNAs have high diagnostic power, and their prognostic potential is evidenced by panels of 5 miRNAs able to predict the outcome of stage II and III colorectal cancer patients. Notably, 8 miRNAs were validated in three additional independent cohorts (validation cohorts) including a plasma cohort thus reinforcing the value of miRNAs as non-invasive biomarkers.pt
dc.language.isoengpt
dc.publisherImpact Journals LLCpt
dc.relationUID/BIM/04773/2013pt
dc.relationCâmara Municipal de Loulé and by the Liga Portuguesa Contra o Cancro (Portuguese League against Cancer) through the Grant LPCC-PT Foundation 2016pt
dc.rightsopenAccesspt
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/pt
dc.subjectmicroRNAspt
dc.subjectbiomarkerpt
dc.subjectcolorectal cancerpt
dc.subjectdiagnosispt
dc.subjectprognosispt
dc.subject.meshAdultpt
dc.subject.meshAgedpt
dc.subject.meshBiomarkers, Tumorpt
dc.subject.meshColorectal Neoplasmspt
dc.subject.meshFemalept
dc.subject.meshGene Expression Profilingpt
dc.subject.meshGene Expression Regulation, Neoplasticpt
dc.subject.meshHumanspt
dc.subject.meshMalept
dc.subject.meshMicroRNAspt
dc.subject.meshMiddle Agedpt
dc.titleIdentification of colorectal cancer associated biomarkers: an integrated analysis of miRNA expressionpt
dc.typearticle-
degois.publication.firstPage21991pt
degois.publication.lastPage22029pt
degois.publication.issue18pt
degois.publication.titleAgingpt
dc.peerreviewedyespt
dc.identifier.doi10.18632/aging.203556pt
degois.publication.volume13pt
dc.date.embargo2021-01-01*
uc.date.periodoEmbargo0pt
item.cerifentitytypePublications-
item.languageiso639-1en-
item.fulltextCom Texto completo-
item.grantfulltextopen-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.openairetypearticle-
crisitem.author.researchunitCNC - Center for Neuroscience and Cell Biology-
crisitem.author.orcid0000-0002-3453-3978-
Appears in Collections:I&D CNC - Artigos em Revistas Internacionais
IIIUC - Artigos em Revistas Internacionais
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This item is licensed under a Creative Commons License Creative Commons