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Aquaporins Transcripts with Potential Prognostic Value in Pancreatic Cancer

dc.contributor.authorLopes, PA
dc.contributor.authorFonseca, E
dc.contributor.authorda Silva, IV
dc.contributor.authorVigia, E
dc.contributor.authorPaulino, J
dc.contributor.authorSoveral, G
dc.date.accessioned2024-02-09T14:48:52Z
dc.date.available2024-02-09T14:48:52Z
dc.date.issued2023
dc.description.abstractPancreatic cancer is anticipated to be the second leading cause of cancer-related death by 2030. Aquaporins (AQPs), a family of water channel proteins, have been linked to carcinogenesis. The aim of this study was to determine AQP gene expression in pancreatic cancer tissues and to validate aquaporins as possible diagnosis and/or prognosis genes. The relative gene expression levels of AQP1, AQP3, AQP5, and AQP9 were analyzed using real-time quantitative PCR (RT-qPCR) in 24 paired pancreatic tumors and adjacent healthy tissues according to variables such as age, gender, and tumor invasiveness and aggressiveness. AQPs transcripts were detected in both healthy and tumor tissues. While AQP1 was downregulated in the tumor samples, AQP3 was particularly overexpressed in low-grade invasive tumors. Interestingly, most of the strong positive Pearson correlation coefficients found between AQPs in healthy tissues were lost when analyzing the tumor tissues, suggesting disruption of the coordinated AQP-gene expression in pancreatic cancer.pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.citationGenes (Basel) . 2023 Aug 25;14(9):1694pt_PT
dc.identifier.doi10.3390/genes14091694pt_PT
dc.identifier.urihttp://hdl.handle.net/10400.17/4799
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.publisherMultidisciplinary Digital Publishing Institute (MDPI)pt_PT
dc.subjectAggressionpt_PT
dc.subjectAquaporins* / geneticspt_PT
dc.subjectHumanspt_PT
dc.subjectPancreatic Neoplasms* / geneticspt_PT
dc.subjectPrognosispt_PT
dc.subjectHCC CHBPTpt_PT
dc.titleAquaporins Transcripts with Potential Prognostic Value in Pancreatic Cancerpt_PT
dc.typejournal article
dspace.entity.typePublication
oaire.citation.issue9pt_PT
oaire.citation.startPage1694pt_PT
oaire.citation.titleGenespt_PT
oaire.citation.volume14pt_PT
rcaap.rightsopenAccesspt_PT
rcaap.typearticlept_PT

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