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The anticancer effects of thymol on HepG2 cell line

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dc.contributor.author Altintas, Fatih
dc.contributor.author Tunc-Ata, Melek
dc.contributor.author Secme, Mucahit
dc.contributor.author Kucukatay, Vural
dc.date.accessioned 2024-03-18T06:47:27Z
dc.date.available 2024-03-18T06:47:27Z
dc.date.issued 2023
dc.identifier.citation Altintas, F., Tunc-Ata, M., Secme, M., Kucukatay, V. (2023). The anticancer effects of thymol on HepG2 cell line. Med. Oncol., 40(9). https://doi.org/10.1007/s12032-023-02134-2 en_US
dc.identifier.issn 1357-0560
dc.identifier.issn 1559-131X
dc.identifier.uri http://dx.doi.org/10.1007/s12032-023-02134-2
dc.identifier.uri https://www.webofscience.com/wos/woscc/full-record/WOS:001042753300001
dc.identifier.uri http://earsiv.odu.edu.tr:8080/xmlui/handle/11489/4690
dc.description WoS Categories: Oncology en_US
dc.description Web of Science Index: Science Citation Index Expanded (SCI-EXPANDED) en_US
dc.description Research Areas: Oncology en_US
dc.description.abstract There is an increasing incidence of liver cancer, which is a hazard for global health. The present study was designed to evaluate possible cytotoxic, genotoxic, apoptotic, oxidant and antioxidant effects of thymol on hepatocellular carcinoma (HepG2) cell line. The cytotoxic effect of thymol on HepG2 cell line was determined by XTT test. We also used the HUVEC cell line to show whether thymol damages healthy cells. Oxidative stress level was determined with Total Oxidant Status (TOS) and Total Antioxidant Status (TAS) measurement kits. Apoptosis of cells was detected in flow cytometry with Annexin V apoptosis kit. Apoptotic gene expressions were analyzed by real-time PCR. Genotoxicity was determined by comet assay, which measures DNA damage. The thymol IC50 dose was found to be 11 & mu;M on HepG2 cell line. This dose had no lethal effect on the healthy HUVEC cell line. While thymol significantly decreased the TOS level, it increased the TAS level significantly in HepG2 cells compared to control. Thymol significantly induced apoptosis in HepG2 cells (apoptosis rate in control group 1%, in thymol group 21%). Thymol did not alter the gene expressions of bax, bcl-2, and casp3, all of which are associated with apoptosis. Statistically significant change in favor of genotoxicity was observed in tail length measurements. Our results suggest that thymol decreases oxidative stress in HepG2 cell line, but it induces apoptosis and genotoxicity. en_US
dc.description.sponsorship Pamukkale University Scientific Research Projects Coordination Unit [2021BSP009] en_US
dc.language.iso eng en_US
dc.publisher HUMANA PRESS INC-TOTOWA en_US
dc.relation.isversionof 10.1007/s12032-023-02134-2 en_US
dc.rights info:eu-repo/semantics/openAccess en_US
dc.subject HepG2, Thymol, Cytotoxicity, Apoptosis, Oxidative stress en_US
dc.subject BAX/BCL-2 RATIO, ESSENTIAL OIL, DNA, CARVACROL, ANTIOXIDANT, APOPTOSIS en_US
dc.title The anticancer effects of thymol on HepG2 cell line en_US
dc.type article en_US
dc.relation.journal MEDICAL ONCOLOGY en_US
dc.contributor.department Ordu Üniversitesi en_US
dc.contributor.authorID 0000-0001-8779-0110 en_US
dc.identifier.volume 40 en_US
dc.identifier.issue 9 en_US


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