Publication:
Evaluation of the effect of Paclitaxel, Epirubicin and Tamoxifen by cell kinetics parameters in estrogen-receptor-positive Ehrlich Ascites Tumor (EAT) cells growing in vitro

dc.contributor.authorÖzalpan, Atilla
dc.contributor.authorArıcan, G. Özcan
dc.date.accessioned2016-04-21T14:09:19Z
dc.date.available2016-04-21T14:09:19Z
dc.date.issued2007-03
dc.description.abstractIn this study the antiproliferative effects of Paclitaxel (PAC), Epirubicin (EPI) and Tamoxifen (TAM) on growth kinetics of Ehrlich Ascites Tumor (EAT) cells were examined in culture. An estrogen-receptor-positive ER (+) hyperdiploid EAT cell line growing in vitro was also analysed in the present study. IC50 doses of PAC, EPI and TAM (12 mu g/ml, 12 mu g/ml and 2 mu g/ml, respectively) were used. Cells were treated with the above doses for 0, 4, 8, 16, 24 and 32 hrs. At the end of these periods, living cell numbers were determined by collecting EAT cells in every group for growth study rate and for MTT assay. Therefore, the mitotic index was determined in the same experimental groups. The proliferation of EAT cells, inhibited by PAC, EPI and TAM concentrations was compared to control with increasing treatment time (4-32 hrs). Treatment of PAC, EPI and TAM alone for 24 hrs decreased the proliferation rate of EAT cells by 50% with respect to control. The inhibition of proliferation rate was higher in double drug treatment than that in single drug treatment with increased treatment time. In the treatment of three drugs applied for 32 hrs, this effect reached a maximum and proliferation rate decreased by 12% as compared to the (100%) control. In our studies, when the mitotic index parameter data were evaluated to determine which phase of the cell cycle was affected by PAC to cause the repression of cell reproduction, it was found that PAC exerted of its cytotoxic effect by causing cell accumulation at mitosis. The accumulation of the cells resulted in an increase in mitotic index values, which was an expected consequence of PAC treatment. It was observed that depending on the drug treatments, inhibition of proliferation rate and mitotic index in EAT cells were increased with respect to control, being with statistically significant occurrence (p < 0.01-p < 0.001). As a result, concomitant treatment combined with hormonal therapy has given improved results compared with single treatment and PAC+ EPI + TAM treatments had a maximum synergistic effect for 32 hrs (p < 0.001).tr_TR
dc.identifier.issn0236-5383
dc.identifier.scopus2-s2.0-34247212229
dc.identifier.scopus2-s2.0-34247212229en
dc.identifier.urihttp://hdl.handle.net/11413/1067
dc.identifier.wos245012100005
dc.identifier.wos245012100005en
dc.language.isoen_UStr_TR
dc.publisherAKADEMIAI KIADO, PRIELLE K U 19, H-1117 BUDAPEST, HUNGARYtr_TR
dc.relationACTA BIOLOGICA HUNGARICAtr_TR
dc.subjectEAT cellstr_TR
dc.subjectcell kineticstr_TR
dc.subjectpaclitaxeltr_TR
dc.subjectepirubicintr_TR
dc.subjecttamoxifentr_TR
dc.subjectbreast-cancertr_TR
dc.subjectlabeling indextr_TR
dc.subjectcyto-toxicitytr_TR
dc.subjecttaxoltr_TR
dc.subjectdeathtr_TR
dc.subjectchemotherapytr_TR
dc.subjectapoptosistr_TR
dc.subjectgrowthtr_TR
dc.subjectsitestr_TR
dc.subjectphasetr_TR
dc.subjecthücre kinetiğitr_TR
dc.subjectpaklitakseltr_TR
dc.subjectepirubisintr_TR
dc.subjecttamoksifentr_TR
dc.subjectmeme kanseritr_TR
dc.subjectetiketleme indeksitr_TR
dc.subjectsito-zehirliliktr_TR
dc.subjecttaksoltr_TR
dc.subjectölümtr_TR
dc.subjectkemoterapitr_TR
dc.subjectapoptoztr_TR
dc.subjectbüyümetr_TR
dc.subjectsitelertr_TR
dc.subjectfaztr_TR
dc.titleEvaluation of the effect of Paclitaxel, Epirubicin and Tamoxifen by cell kinetics parameters in estrogen-receptor-positive Ehrlich Ascites Tumor (EAT) cells growing in vitrotr_TR
dc.typeArticle
dspace.entity.typePublication
local.indexed.atscopus
local.indexed.atwos

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