Please use this identifier to cite or link to this item: https://open.uns.ac.rs/handle/123456789/2900
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dc.contributor.authorDušica Popovićen_US
dc.contributor.authorDušan Laloševićen_US
dc.contributor.authorKosta Popovićen_US
dc.contributor.authorIvan Čapoen_US
dc.contributor.authorJovan Popovićen_US
dc.contributor.authorDejan Miljkovićen_US
dc.date.accessioned2019-09-23T10:24:29Z-
dc.date.available2019-09-23T10:24:29Z-
dc.date.issued2017-10-01-
dc.identifier.issn1596-5996en_US
dc.identifier.urihttps://open.uns.ac.rs/handle/123456789/2900-
dc.description.abstract© Pharmacotherapy Group. Purpose: To investigate the effect of mebendazole on an in vivo solid tumor model of fibrosarcoma in hamsters. Methods: 24 Syrian golden hamsters of both sexes with the approximate body weight of 100g were randomly distributed in 2 experimental and 2 control groups, with 6 animals in each group. BHK-21/C13 cells (2 x 106) in 1 mL Glasgow Minimum Essential Medium (GMEM) were injected subcutaneously into the back of each animal in 3 groups. The experimental groups were treated with mebendazole (460 mg/kg) via a gastric tube on a daily basis, immediately after tumor inoculation. In addition, one experimental group received deoxycholic acid 20 mg/kg once a day. After 2 weeks, when the tumors were approximately 1 - 2 cm in the control group, all the animals were sacrificed, and their blood collected for laboratory analysis. The tumors were excised, their weight and diameters measured, and the volumes calculated. The tumor samples were histopathologically assessed and the main organs toxicologically analyzed. Images were taken and processed by an imaging software, and Ki-67-positive cells in the tumor samples were quantified. Results: Mebendazole diminished tumor mitosis from 18.5 ± 3.02 to 13.5 ± 3.45 (p < 0.05), vasculature and tissue penetration, and increased necroses in tumor slices. Tumor volume and weight were insignificantly attenuated. Toxicity was not observed. Conclusion: Mebendazole might be an effective non-toxic agent in sarcoma therapy.en_US
dc.language.isoenen_US
dc.relation.ispartofTropical Journal of Pharmaceutical Researchen_US
dc.subjectMebendazoleen_US
dc.subjectHamstersen_US
dc.subjectBHK-21/C13 cellsen_US
dc.subjectFibrosarcoma therapyen_US
dc.subjectTumor mitosisen_US
dc.titleEffect of mebendazole on fibrosarcoma in hamstersen_US
dc.typeArticleen_US
dc.identifier.doi10.4314/tjpr.v16i10.19-
dc.identifier.scopus2-s2.0-85032793978-
dc.identifier.isi000418444800017-
dc.identifier.urlhttps://api.elsevier.com/content/abstract/scopus_id/85032793978-
dc.description.versionPublisheden_US
dc.relation.lastpage2451en_US
dc.relation.firstpage2445en_US
dc.relation.issue10en_US
dc.relation.volume16en_US
item.fulltextNo Fulltext-
item.grantfulltextnone-
crisitem.author.deptMedicinski fakultet-
crisitem.author.deptMedicinski fakultet, Katedra za histologiju i embriologiju-
crisitem.author.deptMedicinski fakultet, Katedra za farmaciju-
crisitem.author.deptMedicinski fakultet, Katedra za histologiju i embriologiju-
crisitem.author.orcid0000-0002-0760-9180-
crisitem.author.orcid0000-0002-7739-5202-
crisitem.author.parentorgUniverzitet u Novom Sadu-
crisitem.author.parentorgMedicinski fakultet-
crisitem.author.parentorgMedicinski fakultet-
crisitem.author.parentorgMedicinski fakultet-
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