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Differential expression of miRNAs related to autophagy pathway in tissue and serum samples of colorectal cancer patients

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dc.contributor.author Umit, Y.
dc.contributor.author Nesibe, Y.
dc.contributor.author Kevser, T.
dc.contributor.author Arzu, E.
dc.contributor.author Nihat, A.
dc.contributor.author Umit, Z.
dc.date.accessioned 2022-10-06T12:54:44Z
dc.date.available 2022-10-06T12:54:44Z
dc.date.issued 2022
dc.identifier.issn 00069248 (ISSN)
dc.identifier.uri http://hdl.handle.net/11616/72414
dc.description.abstract BACKGROUND: This study was aimed to investigate the relationship of miR-17-5p, miR-30b, miR-30d, miR-216a and miR-216b associated with autophagy gene beclin 1, and beclin 1 gene with colorectal cancer (CRC). MATERIALS AND METHODS: Forty-seven patients with CRC and 50 healthy individuals with no cancer history were included in this study. In the serum, tumor and non-tumoral tissue samples of the CRC patients, and in the serum samples of the healthy subjects, expression levels of miRNAs were detected by qRT-PCR. The beclin 1 gene expression levels were determined by qRT-PCR, and protein levels were determined by Western blot method in tumor and non-tumor tissue samples of the patients. RESULTS: The miR-17-5p and miR-30d expressions were found to be higher in tumor tissue as compared to patient non-tumor tissues, while expressions of beclin-1, miR-30b and miR-216a were found to be lower. In addition, the beclin-1 protein levels were signifi cantly decreased in the tumor tissue as compared to those in the patient non-tumor tissues. The miR-30d expression was signifi cantly reduced in the serum of the patients when the serum samples of CRC patients and healthy controls were compared. CONCLUSION: The beclin 1 gene may play a role as a tumor suppressor in CRC. Moreover, these miRNAs cannot be used as highly reliable biomarkers in serum for CRC diagnosis © 2022. Bratislava Medical Journal. All Rights Reserved.
dc.source Bratislava Medical Journal
dc.title Differential expression of miRNAs related to autophagy pathway in tissue and serum samples of colorectal cancer patients


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