dc.contributor.author | YILDIZ, PINAR | |
dc.contributor.author | Coskunpinar, Ender Mehmet | |
dc.contributor.author | Hekimoglu, E. | |
dc.contributor.author | Oltulu, Y. Musteri | |
dc.contributor.author | Isbir, T. | |
dc.contributor.author | Turna, A. | |
dc.contributor.author | Yaylim, İlhan | |
dc.contributor.author | AYNACI, ENGİN | |
dc.date.accessioned | 2021-03-03T20:31:34Z | |
dc.date.available | 2021-03-03T20:31:34Z | |
dc.date.issued | 2015 | |
dc.identifier.citation | Coskunpinar E. M. , YILDIZ P., AYNACI E., Turna A., Oltulu Y. M. , Hekimoglu E., Isbir T., Yaylim İ., "Investigation of some DNA repair genes association in non small cell lung cancer.", Cellular and molecular biology (Noisy-le-Grand, France), cilt.61, sa.8, ss.57-62, 2015 | |
dc.identifier.issn | 0145-5680 | |
dc.identifier.other | av_5a67dc9e-2ef6-47ef-807e-30549cfe4b61 | |
dc.identifier.other | vv_1032021 | |
dc.identifier.uri | http://hdl.handle.net/20.500.12627/63536 | |
dc.identifier.uri | https://doi.org/10.14715/cmb/2015.61.8.10 | |
dc.description.abstract | Ribonucleoside-diphosphate reductase subunit M2, also known as ribonucleotide reductase small subunit, is an enzyme that in humans is encoded by the RRM2 gene and also Ribonucleoside-diphosphate reductase large subunit is an enzyme that in humans is encoded by the RRM1 gene. RRM1 is a gene important in determining tumor phenotype, but also induced the expression of PTEN tumor suppressor gene, cell migration, invasion and metastasis formation, and play a preventive role. ERCC2 DNA repair mechanism is associated in more than 20 genes involved in the NER pathway. The aim of this study is to investigate rs13181 ERCC2 (T>G) (Lys751Gln), rs12806698 RRM1 (-269C>A) and rs6759180 (located in the 5'UTR) RRM2 (10126436G>A) gene polymorphisms by using real time PCR technique in patients with NSCLC. 193 NSCLC cases and 141 healthy control cases were included in this study. A significant difference was found between rs12806698 RRM1 genotype distributions (*p: 0.034) and were determined increases the risk of disease approximately 3.044 times AA genotype having (*p: 0.014 OR: 3.044, 95% CI: 1.205-7,688). A significant difference was found between rs6759180 RRM2 genotype distributions (*p: 0.033) and were determined increases the risk of disease approximately 3.49 times GG genotype having (p: 0,009 OR: 3, 49, % 95CI: 1.291-9,482). It was found significant difference in serum 8-OHdG levels between patients and controls (*p: 0001). | |
dc.language.iso | eng | |
dc.subject | Histoloji-Embriyoloji | |
dc.subject | Yaşam Bilimleri (LIFE) | |
dc.subject | HÜCRE BİYOLOJİSİ | |
dc.subject | Tıp | |
dc.subject | Sağlık Bilimleri | |
dc.subject | Temel Tıp Bilimleri | |
dc.subject | Yaşam Bilimleri | |
dc.subject | Moleküler Biyoloji ve Genetik | |
dc.subject | Sitogenetik | |
dc.subject | Temel Bilimler | |
dc.subject | BİYOKİMYA VE MOLEKÜLER BİYOLOJİ | |
dc.subject | Moleküler Biyoloji ve Genetik | |
dc.title | Investigation of some DNA repair genes association in non small cell lung cancer. | |
dc.type | Makale | |
dc.relation.journal | Cellular and molecular biology (Noisy-le-Grand, France) | |
dc.contributor.department | İstanbul Üniversitesi , , | |
dc.identifier.volume | 61 | |
dc.identifier.issue | 8 | |
dc.identifier.startpage | 57 | |
dc.identifier.endpage | 62 | |
dc.contributor.firstauthorID | 99364 | |