CYP and GST polymorphisms and survival in advanced non-small cell lung cancer patients
dc.authorid | Kurt, Emine Bahar | |
dc.authorid | İşcan, Mümtaz | |
dc.authorid | 0000-0001-9987-0572 | |
dc.authorid | 0000-0002-3495-2339 | |
dc.contributor.author | Ada, Ahmet Oğuz | |
dc.contributor.author | Kunak, Celalettin Semih | |
dc.contributor.author | Bilgen, Serdar | |
dc.contributor.author | Alpar, Sibel | |
dc.contributor.author | Gülhan, Meral | |
dc.date.accessioned | 2021-06-23T18:52:01Z | |
dc.date.available | 2021-06-23T18:52:01Z | |
dc.date.issued | 2010 | |
dc.department | BAİBÜ, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü | en_US |
dc.description.abstract | Several polymorphisms in cytochrome P-450s (CYP)s and Glutathione S-transferases (GST)s have been reported to be associated with survival rates of patients with non-small cell lung cancer (NSCLC) but the studies in this regard are scarce and the results are contradictory. In this study, CYP1A1 (Ile462Val), CYP1B1(Asn453Ser), GST M1, GSTP1 exon 5 (Ile105Val) and exon 6(Ala114Val) and GSTT1 polymorphisms were determined in 138 patients with advanced NSCLC to evaluate their role in survival. Of the studied CYP and GST polymorphisms only GSTP1 exon 6 variant significantly altered (improved) the survival compared to wild type (p=0.036) with median survival of 22.2 months and 16.1 months, respectively. Multivariate analysis also revealed a significant reduction of adjusted hazard ratio of death associated only with the GSTP1 exon 6 variant genotype of 0.45 (95% confidence interval (95% CI), 0.23-0.89, p=0.022). These results show that the GSTP1 exon 6 variant genotype is associated with improved survival in the patients with advanced NSCLC. | en_US |
dc.identifier.doi | 10.4149/neo_2010_06_512 | |
dc.identifier.endpage | 521 | en_US |
dc.identifier.issn | 0028-2685 | |
dc.identifier.issue | 6 | en_US |
dc.identifier.pmid | 20845989 | en_US |
dc.identifier.scopus | 2-s2.0-79952113910 | en_US |
dc.identifier.scopusquality | Q2 | en_US |
dc.identifier.startpage | 512 | en_US |
dc.identifier.uri | https://doi.org/10.4149/neo_2010_06_512 | |
dc.identifier.uri | https://hdl.handle.net/20.500.12491/4097 | |
dc.identifier.volume | 57 | en_US |
dc.indekslendigikaynak | Scopus | en_US |
dc.indekslendigikaynak | PubMed | en_US |
dc.institutionauthor | Kurt, Emine Bahar | |
dc.language.iso | en | en_US |
dc.publisher | SAP - Slovak Academic Press, spol. s.r.o. | en_US |
dc.relation.ispartof | Neoplasma | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.rights | info:eu-repo/semantics/openAccess | en_US |
dc.subject | Cytochrome P-450 | en_US |
dc.subject | Glutathione S-Transferase | en_US |
dc.subject | Non Small Cell Lung Cancer | en_US |
dc.subject | Polymorphism | en_US |
dc.subject | Survival | en_US |
dc.title | CYP and GST polymorphisms and survival in advanced non-small cell lung cancer patients | en_US |
dc.type | Article | en_US |