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dc.contributor.authorFateh, A|| Feizi, MAH|| Safaralizadeh, R|| Somi, MH|| Ravanbakhsh, R|| Shokoohi, B|| Hashemzadeh, S|| Azarbarzin, S
dc.date.accessioned2018-08-26T09:32:54Z
dc.date.available2018-08-26T09:32:54Z
dc.date.issued2016
dc.identifier10.4081/gi.2016.6641
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/57441
dc.description.abstractMicroRNAs (miRNAs) are impressive regulators of gene expression that have a critical role in the pathogenesis of Colorectal Cancer (CRC). With respect to the aberrant expression of microRNA-383 (miR-383) in some types of human malignancy, this prospective study characterized its contribution to CRC tumorigenesis. The real-time reverse transcription- polymerase chain reaction was used to examine miR-383 expression levels prospectively in 40 sample pairs of CRC tissues and adjacent noncancerous tissues (> 2 cm from cancer tissue). No significant relationship was found between miR-383 expression levels and clinicopathological features. The ability of miR-383 to function as a tumor marker was also examined. Showing significant changes overall, miR-383 expression levels were significantly down regulated in the group of CRC samples compared with matched noncancerous tissue samples. A receiver operating characteristic (ROC) curve also showed ROC area (AROC) of 70% for miR-383 with 68% and 75% sensitivity and specificity, respectively. Therefore, miR-383 can be considered as a tumor marker in CRC and help as a potential predictive biomarker in the diagnosis of colorectal cancer.
dc.language.isoEnglish
dc.relation.ispartofGastroenterology Insights
dc.subjectmicroRNA|| microRNA 383|| unclassified drug|| Article|| cancer prognosis|| clinical article|| colorectal cancer|| controlled study|| down regulation|| female|| gene expression|| human|| human tissue|| male|| predictive value|| prospective study|| receiver operating characteristic|| reverse transcription polymerase chain reaction|| sensitivity and specificity
dc.titlePrognostic and predictive roles of MIR-383 in colorectal cancer
dc.typeArticle
dc.citation.volume7
dc.citation.issue1
dc.citation.indexScopus


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