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dc.contributor.authorTaskan, Tuba
dc.contributor.authorNoori, Farshad
dc.contributor.authorKurukahvecioglu, Osman
dc.contributor.authorKaraman, Niyazi
dc.contributor.authorGonenc, Aymelek
dc.date.accessioned2025-12-28T16:40:11Z
dc.date.available2025-12-28T16:40:11Z
dc.date.issued2025
dc.identifier.issn0007-5027
dc.identifier.issn1943-7730
dc.identifier.urihttps://doi.org/10.1093/labmed/lmae097
dc.identifier.urihttps://hdl.handle.net/20.500.12933/2447
dc.description.abstractBackground Gene polymorphisms of rearranged during transfection (RET) and its ligand neurturin (NRTN) are one of the focus of studies in the investigation of cancer pathogenesis, invasion, and metastasis. In this study, we aimed to examine the possible risk of breast cancer between RET G691S, L769L, S904S, and NRTN IVSI-663 polymorphisms and to evaluate serum NRTN, brain-derived neurotrophic factor (BDNF), matrix metalloproteinase (MMP)-2, MMP-9, and focal adhesion kinase (FAK) levels. Methods The study consists of 110 breast cancer patients and 110 controls. Polymorphisms were detected by the polymerase chain reaction method from study groups whole blood. Results The NRTN IVSI-663 polymorphism in G allele has been found to be 1.54 fold increased the risk of breast cancer, however AA genotype has been found 0.43 fold decreased the risk of breast cancer (P < .05, P < .05, respectively). Study groups showed a similar profile for RET G691S, L769L, S904S allele frequencies and genotype distributions (P > .05). In the patient group, significant increase in serum NRTN and FAK levels and decrease in MMP-2 and MMP-9 levels were found (P < .05, P < .05, P < .05, P < .05, respectively). Discussion In summary that increased breast cancer risk with the G allele in NRTN gene IVSI-663 polymorphism, as well as the increased serum NRTN and FAK levels, will contribute to the diagnosis, prognosis and determination of new treatment strategies.
dc.description.sponsorshipGazi University [02/2019-03]
dc.description.sponsorshipThis work was supported by the Gazi University Scientific Research Projects under Grant number 02/2019-03.
dc.language.isoen
dc.publisherOxford Univ Press
dc.relation.ispartofLaboratory Medicine
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectbreast cancer
dc.subjectrearranged during transfection
dc.subjectneurturin
dc.subjectpolymorphism
dc.subjectfocal adhesion kinase
dc.subjectbrain-derived neurotrophic factor
dc.titleNeurturin gene IVSI-663 polymorphism but not RET variants is associated with increased risk for breast cancer
dc.typeArticle
dc.identifier.orcid0000-0003-1677-5356
dc.identifier.orcid0000-0002-0082-6238
dc.identifier.orcid0000-0001-9661-8291
dc.departmentAfyonkarahisar Sağlık Bilimleri Üniversitesi
dc.identifier.doi10.1093/labmed/lmae097
dc.identifier.volume56
dc.identifier.issue4
dc.identifier.startpage351
dc.identifier.endpage359
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.department-temp[Taskan, Tuba] Afyonkarahisar Hlth Sci Univ, Fac Pharm, Dept Biochem, Afyonkarahisar, Turkiye; [Noori, Farshad] Chris Obrien Lifehouse Hosp, Gen Surg Outpatient Clin, Sydney, Australia; [Kurukahvecioglu, Osman] Gazi Univ, Fac Med, Dept Gen Surg, Ankara, Turkiye; [Karaman, Niyazi] Dr Abdurrahman Yurtaslan Ankara Oncol Training & R, Gen Surg Outpatient Clin, Ankara, Turkiye; [Gonenc, Aymelek] Gazi Univ, Fac Pharm, Dept Biochem, Ankara, Turkiye
dc.identifier.pmid39671698
dc.identifier.scopus2-s2.0-105010714273
dc.identifier.scopusqualityQ3
dc.identifier.wosWOS:001377174600001
dc.identifier.wosqualityQ4
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.snmzKA_WoS_20251227


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