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dc.contributor.authorParlak, A.E. and Tekin, S. and Karatepe, A. and Koparir, P. and Telceken, H. and Ceribası, A.O. and Karatepe, M.
dc.date.accessioned2021-04-08T12:06:49Z
dc.date.available2021-04-08T12:06:49Z
dc.date.issued2019
dc.identifier10.1002/jcb.28460
dc.identifier.issn07302312
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85061631271&doi=10.1002%2fjcb.28460&partnerID=40&md5=1701b6c43328cc45870f5092e1f3d785
dc.identifier.urihttp://acikerisim.bingol.edu.tr/handle/20.500.12898/4106
dc.description.abstract1,2,4-Triazoles are used as antifungal, antibacterial, antimicrobial, and antioxidant against some oxidative radical species. Recently, many 1,2,4-triazoles continue to be synthesized. In this study, the effect of the 1,2,4-triazole derivatives on human colon cancer (HT29) was investigated in vitro and in vivo in rats. MTT test was applied to in in vitro experiments. For in vivo study, rats were divided into seven groups as follows: Control group (negative control), azoxymethane (AOM), AOM + cisplatin 15, AOM + L1, AOM + L2, AOM + L3, and AOM + L4. To create colon cancer, the AOM injection was injected subcutaneously at a dose of 15 mg/kg, three times (once weekly). The in vivo studies were completed at 28 weeks. It was found that the 1,2,4-triazole derivatives reduced the cell viability (P < 0.05). In all animals in the experimental groups, mild dysplasia was detected in 100% of the colon mucosal epithelium. Severe dysplasia and adenocarcinoma were observed in L1 groups. As a result, this study determined that the 1,2,4-triazole derivatives exhibit antitumor activity. © 2019 Wiley Periodicals, Inc.
dc.language.isoEnglish
dc.sourceJournal of Cellular Biochemistry
dc.titleIn vitro and histological investigation of antitumor effect of some triazole compounds in colon cancer cell line


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