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[Biological effects of thyroxine in experimental carcinogenesis].

A A AbduvaliyevInstitute of Biochemistry, Academy of Sciences of the Republic of UzbekistanM S GildiyevaInstitute of Biochemistry, Academy of Sciences of the Republic of UzbekistanSaatov TsInstitute of Biochemistry, Academy of Sciences of the Republic of Uzbekistan
PubMedrepository2005en
ABI

Аннотация

The study was undertaken to examine the in vitro and in vivo effects ofthyroxine Т4 at the concentrations of 10-4 M, 10-6 M, 10- M on the proliferative capacity and apoptosis of tumor cells of various pathogenesis. During the investigations, the authors used the unicellular suspension prepared from the surgical material obtained from 2 patients operated on for thyroid nodules (n = 1) and breast tumors in gynecomastia (n = 1) and evaluated the in vivo antitumor and antiproliferative activities of Т4, by using the melanoma B-16 inoculated in C57B1 mice. In the in vitro experiments, Т4 given in a dose of 10- М produced the highest cytotoxic activity against benign thyroid tumor cells (70±4.58%; p < 0.05). When used in this dose, T4 induced the greatest apoptotic death of the cells (9.0±0.90%; p < 0.05) as compared with the controls (1.0±0.30%). The in vitro effect of T4 in doses of 10-4 M, 10-6 M, 10- M on breast tumor cells in the presence of gynecomastia led to a decrease in levels of the oncogenic protein HER2/neu by an average of 27.25±1.14% (p < 0.001). In the in vivo experiments on a model of the tumor strain of melanoma B-16, T4 at the concentrations of 10-4 M, 10-6 M, 10- M showed a high antitumor activity (59.00±5.54%; p < 0.001 of tumor growth suppression by mass and 74.12±0.26%; p < 0.001 by volume). When given in a dose of 10- M, T4 displayed the highest antiproliferative activity (MI, 1.3±0.16%o, p < 0.001; AI, 10.65±1.39%, p < 0.001) as compared with the control group (MI, 4.96±0.43%o; AI, 4.43+0.40%).

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