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A Schiff base derivative for effective treatment of diethylnitrosamine-induced liver cancer in vivo

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dc.creator Tuzcu, Mehmet
dc.creator Orhan, Cemal
dc.creator Sahin, Kazim
dc.creator Sahin, Nurhan
dc.creator DEDE, Bülent
dc.creator Ozercan, Ibrahim Hanifi
dc.creator Sahin, Fikrettin
dc.creator Dogan, Aysegul
dc.creator Demirci, Selami
dc.creator Basak, Nese
dc.creator Telci, Dilek
dc.date 2015-05-31T21:00:00Z
dc.date.accessioned 2020-10-06T09:30:02Z
dc.date.available 2020-10-06T09:30:02Z
dc.identifier 201b3d23-ffbb-4fb0-a60b-0cb31334424f
dc.identifier 10.1097/cad.0000000000000221
dc.identifier https://avesis.sdu.edu.tr/publication/details/201b3d23-ffbb-4fb0-a60b-0cb31334424f/oai
dc.identifier.uri http://acikerisim.sdu.edu.tr/xmlui/handle/123456789/55078
dc.description Hepatocellular carcinoma is one of the most prevalent cancers, with a high morbidity rate, even in developed countries. In the present study, the curative effect of the Schiff base (SB) heterodinuclear copper(II) Mn(II) complex on diethylnitrosamine (DEN)-induced liver carcinoma was investigated. Hepatocarcinoma was initiated by an injection of DEN and promoted by phenobarbital (0.05%) in the diet. In addition, the potential nephrotoxicity of SB was evaluated in a cisplatin-induced nephrotoxicity model. Rats were administered the SB complex (1 and 2 mg/kg body weight/day) for 24 weeks, and cancer progression was investigated by macroscopic, histopathological, and western blot examinations. The administration of SB decreased the incidence and the number of hepatic nodules in a dose-dependent manner by regulating inflammation response and the apoptotic pathway. Western blot analyses from the livers of rats treated with SB after DEN induction showed significantly enhanced Bax and caspase-3 levels, with a marked decrease in the levels of Bcl-2, NF-kappa B p65 and cyclooxygenase (COX)-2. Results from the nephrotoxicity study showed that, whereas cisplatin increased serum urea nitrogen and creatinine levels, no increase in serum biochemical parameters was detected in SB-treated animals. Moreover, protein levels of NF-E2-related factor-2 (Nrf2) and heme oxygenase-1 were lower, whereas nuclear factor-kappa B (NF-kappa B p65) and activator protein-1 levels were higher in the kidneys of cisplatin-treated animals compared with that of the SB groups. Therefore, the SB complex could be an alternative chemotherapeutic option for liver cancer treatment once its safety in clinical applications has been examined. Copyright (C) 2015 Wolters Kluwer Health, Inc. All rights reserved.
dc.language eng
dc.rights info:eu-repo/semantics/closedAccess
dc.title A Schiff base derivative for effective treatment of diethylnitrosamine-induced liver cancer in vivo
dc.type info:eu-repo/semantics/article


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