ASSOCIATION OF SERUM PARAOXONASE 1 ACTIVITIES, POLYMORPHISMS AND OXIDATIVE STRESS IN BREAST CANCER PATIENTS WITH TYPE 2 DIABETES MELLITUS

dc.authorid0000-0001-9410-8554
dc.authorid0000-0002-6710-538X
dc.authorid0000-0002-0814-0820
dc.contributor.authorEraldemir, Fatma Ceyla
dc.contributor.authorUren, Nihal
dc.contributor.authorKum, Tugba
dc.contributor.authorErbay, Burcu
dc.contributor.authorSahin, Deniz
dc.contributor.authorErgul, Emel
dc.contributor.authorAcar, Esra
dc.date.accessioned2025-05-10T19:35:57Z
dc.date.issued2019
dc.departmentİstanbul Medeniyet Üniversitesi
dc.description.abstractBackground: The aim of the study was to investigate the association of paraoxonase 1 (PON1) polymorphism, PON1/arylesterase (ARE) activity and oxidative stress index (OSI) in breast cancer (BC) patients with type 2 diabetes (DM). Methods: Our study group consisted of 30 healthy women (HV group) and 66 female BC patients. The BC patients were divided into two groups: those with (n=37) and without DM (n=29) (BDM and NBDM group). Genotyping of PON1 Q192R and L55M polymorphisms were done by polymerase chain reaction (PCR) - restriction fragment length polymorphism (RFLP) method. Serum PON1/ARE enzyme activities, total oxidant status (TOS) and total antioxidant status (TAS) were analysed by spectrophotometric method. The ratio of TOS to TAS was accepted as the oxidative stress index (OSI). Results: PON1 Q192R genotype frequency distribution was significantly different in the BDM group compared to the NBDM group (p=0.021). When alleles distribution was examined, R and L alleles were significantly lower, Q and M alleles were significantly higher in the BDM group than in the NBDM group (p<0.001). TOS and OSI were statistically higher in BC patients than HV group (p<0.001). Conclusions: Our results suggest that PON1 gene Q and M alleles may be the risk factors predisposing formation of BC due to increased oxidant damage seen in DM. However, these statements require further confirmation with screening PON1 polymorphism in a greater number of patients with DM, and also wide range follow-up studies are necessary for the same purpose.
dc.description.sponsorshipKOU individual research Project unit [2014/099-HD]
dc.description.sponsorshipThis work was supported by KOU individual research Project unit (Project number: 2014/099-HD).
dc.identifier.doi10.2478/jomb-2018-0043
dc.identifier.endpage375
dc.identifier.issn1452-8258
dc.identifier.issn1452-8266
dc.identifier.issue3
dc.identifier.pmid31156348
dc.identifier.scopusqualityQ3
dc.identifier.startpage368
dc.identifier.urihttps://doi.org/10.2478/jomb-2018-0043
dc.identifier.urihttps://hdl.handle.net/20.500.14730/9022
dc.identifier.volume38
dc.identifier.wosWOS:000468363100015
dc.identifier.wosqualityQ4
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.publisherSciendo
dc.relation.ispartofJournal of Medical Biochemistry
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/openAccess
dc.snmzKA_WOS_20250302
dc.subjectdiabetes mellitus type 2
dc.subjectparaoxonase 1
dc.subjectsingle nucleotide polymorphism
dc.subjectoxidative stress
dc.subjectbreast cancer
dc.titleASSOCIATION OF SERUM PARAOXONASE 1 ACTIVITIES, POLYMORPHISMS AND OXIDATIVE STRESS IN BREAST CANCER PATIENTS WITH TYPE 2 DIABETES MELLITUS
dc.typeArticle

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