Εμφάνιση απλής εγγραφής

dc.creatorMagouliotis D.E., Tasiopoulou V.S., Dimas K., Sakellaridis N., Svokos K.A., Svokos A.A., Zacharoulis D.en
dc.date.accessioned2023-01-31T08:55:46Z
dc.date.available2023-01-31T08:55:46Z
dc.date.issued2019
dc.identifier10.1016/j.pan.2019.02.006
dc.identifier.issn14243903
dc.identifier.urihttp://hdl.handle.net/11615/76091
dc.description.abstractBackground: This study aimed to assess the differential gene expression of aquaporin (AQP) gene family interactome in pancreatic ductal adenocarcinoma (PDAC) using data mining techniques to identify novel candidate genes intervening in the pathogenicity of PDAC. Method: Transcriptome data mining techniques were used in order to construct the interactome of the AQP gene family and to determine which genes members are differentially expressed in PDAC as compared to controls. The same techniques were used in order to evaluate the potential prognostic role of the differentially expressed genes. Results: Transcriptome microarray data of four GEO datasets were incorporated, including 142 primary tumor samples and 104 normal pancreatic tissue samples. Twenty differentially expressed genes were identified, of which nineteen were downregulated and one up-regulated. A molecular panel of four genes (Aquaporin 7 – AQP7; Archain 1 – ARCN1; Exocyst Complex Component 3 – EXOC3; Coatomer Protein Complex Subunit Epsilon – COPE) were identified as potential prognostic markers associated with overall survival. Conclusion: These outcomes should be further assessed in vitro in order to fully understand the role of these genes in the pathophysiological mechanism of PDAC. © 2019 IAP and EPCen
dc.language.isoenen
dc.sourcePancreatologyen
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85062015923&doi=10.1016%2fj.pan.2019.02.006&partnerID=40&md5=467d80a9a9566f82baf40c39d17e6fdb
dc.subjectaquaporinen
dc.subjectaquaporin 1en
dc.subjectaquaporin 10en
dc.subjectaquaporin 11en
dc.subjectaquaporin 12aen
dc.subjectaquaporin 12ben
dc.subjectaquaporin 2en
dc.subjectaquaporin 3en
dc.subjectaquaporin 4en
dc.subjectaquaporin 6en
dc.subjectaquaporin 7en
dc.subjectaquaporin 8en
dc.subjectarchain 1en
dc.subjectcoatomer proteinen
dc.subjectcoatomer protein complex subunit alphaen
dc.subjectcoatomer protein complex subunit beta 1en
dc.subjectcoatomer protein complex subunit beta 2en
dc.subjectcoatomer protein complex subunit epsilonen
dc.subjectcoatomer protein complex subunit gamma 1en
dc.subjectcoatomer protein complex subunit gamma 2en
dc.subjectexocyst complex component 3en
dc.subjectrh associated glycoproteinen
dc.subjectribonucleotide reductase regulatory tp53 inducible subunit m2ben
dc.subjectsodium glucose cotransporter 1en
dc.subjecttranscriptomeen
dc.subjecttumor markeren
dc.subjectunclassified drugen
dc.subjectaquaporinen
dc.subjectArticleen
dc.subjectcancer prognosisen
dc.subjectcancer survivalen
dc.subjectcontrolled studyen
dc.subjectdown regulationen
dc.subjectgene expressionen
dc.subjecthumanen
dc.subjecthuman tissueen
dc.subjectmajor clinical studyen
dc.subjectmultigene familyen
dc.subjectoverall survivalen
dc.subjectpancreas adenocarcinomaen
dc.subjectpancreas tissueen
dc.subjectpathogenicityen
dc.subjectpriority journalen
dc.subjecttranscriptomicsen
dc.subjectupregulationen
dc.subjectadenocarcinomaen
dc.subjectgene expression profilingen
dc.subjectgene expression regulationen
dc.subjectgenetic databaseen
dc.subjectgeneticsen
dc.subjectmetabolismen
dc.subjectmultigene familyen
dc.subjectpancreas carcinomaen
dc.subjectpancreas tumoren
dc.subjectpathologyen
dc.subjectphysiologyen
dc.subjectprotein microarrayen
dc.subjectAdenocarcinomaen
dc.subjectAquaporinsen
dc.subjectCarcinoma, Pancreatic Ductalen
dc.subjectDatabases, Geneticen
dc.subjectDown-Regulationen
dc.subjectGene Expression Profilingen
dc.subjectGene Expression Regulation, Neoplasticen
dc.subjectHumansen
dc.subjectMultigene Familyen
dc.subjectPancreatic Neoplasmsen
dc.subjectProtein Array Analysisen
dc.subjectUp-Regulationen
dc.subjectElsevier B.V.en
dc.titleTranscriptomic analysis of the Aquaporin (AQP) gene family interactome identifies a molecular panel of four prognostic markers in patients with pancreatic ductal adenocarcinomaen
dc.typejournalArticleen


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