dc.contributor.author | Kara, Murat | |
dc.contributor.author | Yumrutaş, Önder | |
dc.contributor.author | Özcan, Önder | |
dc.contributor.author | Çelik, Özgür İlhan | |
dc.contributor.author | Bozgeyik, Esra | |
dc.contributor.author | Bozgeyik, İbrahim | |
dc.contributor.author | Taşdemir, Şener | |
dc.date.accessioned | 2020-11-20T15:05:12Z | |
dc.date.available | 2020-11-20T15:05:12Z | |
dc.date.issued | 2015 | |
dc.identifier.issn | 0378-1119 | |
dc.identifier.issn | 1879-0038 | |
dc.identifier.uri | https://doi.org/10.1016/j.gene.2015.04.065 | |
dc.identifier.uri | https://hdl.handle.net/20.500.12809/2985 | |
dc.description | 0000-0001-8252-3339 | en_US |
dc.description | WOS: 000356979700010 | en_US |
dc.description | PubMed ID: 25925209 | en_US |
dc.description.abstract | Colorectal cancer is one of the frequently seen malignancies in the world. To date, several oncogenes and tumor suppressor genes have been identified and linked to colorectal cancer pathogenesis. Although recent advances in the diagnosis and therapy of colorectal cancer are promising, identifying novel genetic contributors is still high priority. In the present study, expression profile of some cancer-related genes and their regulatory miRNA molecules were evaluated by using a high-throughput real-time PCR method. For the study, a total of 54 patients diagnosed with CRC and normal colon tissue samples of 42 healthy controls were included. For the expression analysis, total RNA was extracted from FFPE tissue samples and converted to cDNA. All expression analyses were assessed by using Fluidigm Microfluidic Dynamic Array chips for 96 samples and the reactions were held in Fluidigm BioMark (TM) HD System Real-Time PCR. As a result of the study, expression of the ADAMTS1, FHIT, RUNX1, RUNX3 and WWOX genes was shown to be significantly altered in CRC tissues in contrast to normal tissue samples. Moreover, miR-378a-3p, miR-155-5p, miR-193b-3p, miR-96-5p, miR-17-5p, miR-27a-3p, miR-133b, miR-203a, miR-205-5p, miR-34c-5p, miR-130a-3p, miR-301a-3p, miR-132-3p, miR-222-3p, miR-34a-5p, miR-21-5p, miR-29a-3p and miR-29b-3p were found to be significantly deregulated in CRC. Consequently, results of the current study strongly suggest the involvement of novel cancer-related genes and their regulatory miRNAs in CRC physiopathology. (C) 2015 Elsevier B.V. All rights reserved. | en_US |
dc.description.sponsorship | Scientific Research Projects Management Unit of Mugla Sitki Kocman UniversityMugla Sitki Kocman University [13/152] | en_US |
dc.description.sponsorship | This study was supported by a project from the Scientific Research Projects Management Unit of Mugla Sitki Kocman University (Grant number: 13/152). | en_US |
dc.item-language.iso | eng | en_US |
dc.publisher | Elsevier Science Bv | en_US |
dc.item-rights | info:eu-repo/semantics/openAccess | en_US |
dc.subject | Colorectal Cancer | en_US |
dc.subject | Mirna | en_US |
dc.subject | ADAMTS1 | en_US |
dc.subject | FHIT | en_US |
dc.subject | Runxs | en_US |
dc.subject | SIRT1 | en_US |
dc.subject | WWOX | en_US |
dc.title | Differential expressions of cancer-associated genes and their regulatory miRNAs in colorectal carcinoma | en_US |
dc.item-type | article | en_US |
dc.contributor.department | MÜ, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü | en_US |
dc.contributor.institutionauthor | Kara, Murat | |
dc.contributor.institutionauthor | Özcan, Önder | |
dc.contributor.institutionauthor | Çelik, Özgür İlhan | |
dc.identifier.doi | 10.1016/j.gene.2015.04.065 | |
dc.identifier.volume | 567 | en_US |
dc.identifier.issue | 1 | en_US |
dc.identifier.startpage | 81 | en_US |
dc.identifier.endpage | 86 | en_US |
dc.relation.journal | Gene | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |