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dc.contributor.authorAydın, Pınar Koroglu
dc.contributor.authorYANARDAĞ, Refiye
dc.contributor.authorTÜRKYILMAZ, İSMET BURCU
dc.contributor.authorBULAN, Nihal Ömür
dc.contributor.authorGul, İlknur
dc.date.accessioned2023-02-21T10:26:45Z
dc.date.available2023-02-21T10:26:45Z
dc.identifier.citationAydın P. K., TÜRKYILMAZ İ. B., Gul İ., BULAN N. Ö., YANARDAĞ R., "Drug repurposing: Metformin’s effect against liver tissue damage in diabetes and prostate cancer model", Journal of Diabetes and Metabolic Disorders, 2022
dc.identifier.issn2251-6581
dc.identifier.othervv_1032021
dc.identifier.otherav_442ee484-4652-42a7-b0d4-d49ad111384e
dc.identifier.urihttp://hdl.handle.net/20.500.12627/188405
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85143213268&origin=inward
dc.identifier.urihttps://doi.org/10.1007/s40200-022-01109-w
dc.description.abstract© 2022, The Author(s), under exclusive licence to Tehran University of Medical Sciences.Background: There are evidences linking diabetes to the pathogenesis and progression of various cancers. Metformin is a well-known antidiabetic drug that reduces the levels of circulating glucose and insulin in patients with both insulin resistance and hyperinsulinemia. Aim of the present study was to evaluate the effect of metformin on the liver of rats bearing prostate cancer, diabetes and prostate cancer + diabetes via histopathological and biochemical methods. Methods: Male Copenhagen rats were divided into six groups. Control group, diabetic group, cancer group, diabetic + cancer group, diabetic + cancer + metformin group, cancer + metformin group. Diabetes was induced by injecting single dose of streptozotocin (65 mg/kg) to Copenhagen rats, cancer induced 2 × 104 Mat-LyLu cells. Metformin treatment was administered daily by gavage following inocculation of the Mat- Lylu cells to fifth and sixth group. The experiment was terminated on the 14th day following Mat-LyLu cell injection. At the end of the experimental period, the rats were sacrificed, and liver tissue was taken. Liver damage was scored. Biochemically, serum prostate-specific antigen level was determined by employing Enzyme Linked Immuno Sorbent Assay method. In addition, the activities of different enzyme and biochemical parameters were determined spectrophotometrically inform the hepatic tissue specimens. Results: The findings of this study reveal that histopathological and biochemical damage in cancer and diabetic + cancer groups decreased significantly in the metformin treated groups. Conclusion: These highlights that the antidiabetic drug metformin can be repositioned for attenuating liver tissue damage associated with prostate cancer and diabetes.
dc.language.isoeng
dc.subjectSağlık Bilimleri
dc.subjectTemel Tıp Bilimleri
dc.subjectDahiliye
dc.subjectEndokrinoloji, Diyabet ve Metabolizma
dc.subjectİç Hastalıkları
dc.subjectEndokrinoloji ve Metabolizma Hastalıkları
dc.subjectTıp
dc.subjectTIP, GENEL & DAHİLİ
dc.subjectENDOKRİNOLOJİ VE METABOLİZMA
dc.subjectKlinik Tıp
dc.subjectKlinik Tıp (MED)
dc.subjectDahili Tıp Bilimleri
dc.titleDrug repurposing: Metformin’s effect against liver tissue damage in diabetes and prostate cancer model
dc.typeMakale
dc.relation.journalJournal of Diabetes and Metabolic Disorders
dc.contributor.departmentİstanbul Üniversitesi , Fen Fakültesi , Biyoloji Bölümü
dc.contributor.firstauthorID4227619


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