dc.contributor.author | Fateh, A | |
dc.contributor.author | Feizi, MAH | |
dc.contributor.author | Safaralizadeh, R | |
dc.contributor.author | Somi, MH | |
dc.contributor.author | Ravanbakhsh, R | |
dc.contributor.author | Shokoohi, B | |
dc.contributor.author | Hashemzadeh, S | |
dc.contributor.author | Azarbarzin, S | |
dc.date.accessioned | 2018-08-26T07:40:52Z | |
dc.date.available | 2018-08-26T07:40:52Z | |
dc.date.issued | 2016 | |
dc.identifier | 10.4081/gi.2016.6641 | |
dc.identifier.uri | http://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/47286 | |
dc.description.abstract | MicroRNAs (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 miRNA- 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 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.iso | English | |
dc.relation.ispartof | GASTROENTEROLOGY INSIGHTS | |
dc.subject | Biomarker | |
dc.subject | Colorectal cancer | |
dc.subject | MicroRNA | |
dc.subject | MiR-383 | |
dc.title | Prognostic and predictive roles of microRNA-383 in colorectal cancer | |
dc.type | Article | |
dc.citation.volume | 7 | |
dc.citation.issue | 1 | |
dc.citation.index | Web of science | |
dc.identifier.DOI | https://doi.org/10.4081/gi.2016.6641 | |