Ethacrynic acid and cinnamic acid combination exhibits selective anticancer effects on K562 chronic myeloid leukemia cells

dc.contributor.author Yenigul, Munevver
dc.contributor.author Akcok, Ismail
dc.contributor.author Gencer Akcok, Emel Basak
dc.contributor.authorID 0000-0002-6559-9144 en_US
dc.contributor.authorID 0000-0002-5444-3929 en_US
dc.contributor.authorID 0000-0003-0468-721X en_US
dc.contributor.department AGÜ, Yaşam ve Doğa Bilimleri Fakültesi, Biyomühendislik Bölümü en_US
dc.contributor.institutionauthor Yenigul, Munevver
dc.contributor.institutionauthor Akcok, Ismail
dc.contributor.institutionauthor Gencer Akcok, Emel Basak
dc.date.accessioned 2023-03-01T08:52:05Z
dc.date.available 2023-03-01T08:52:05Z
dc.date.issued 2022 en_US
dc.description.abstract Background Despite the recent advances in chemotherapy, the outcomes and the success of these treatments still remain insufficient. Novel combination treatments and treatment strategies need to be developed in order to achieve more effective treatment. This study was designed to investigate the combined effect of ethacrynic acid and cinnamic acid on cancer cell lines. Methods The anti-proliferative effect of ethacrynic acid and cinnamic acid was investigated by MTT cell viability assay in three different cancer cell lines. Combination indexes were calculated using CompuSyn software. Apoptosis was assessed by flow cytometric Annexin V-FITC/PI double-staining. The effect of the inhibitors on cell cycle distribution was measured by propidium iodide staining. Results The combination treatment of ethacrynic acid and cinnamic acid decreased cell proliferation significantly, by 63%, 75% and 70% for K562, HepG2 and TFK-1 cells, respectively. A 5.5-fold increase in the apoptotic cell population was observed after combination treatment of K562 cells. The population of apoptotic cells increased by 9.3 and 0.4% in HepG2 and TFK-1 cells, respectively. Furthermore, cell cycle analysis shows significant cell cycle arrest in S and G2/M phase for K562 cells and non-significant accumulation in G0/G1 phase for TFK-1 and HepG2 cells. Conclusions Although there is a need for further investigation, our results suggest that the inhibitors used in this study cause a decrease in cellular proliferation, induce apoptosis and cause cell cycle arrest. en_US
dc.identifier.endpage 7530 en_US
dc.identifier.issn 0301-4851
dc.identifier.issn 15873-4978
dc.identifier.issue 8 en_US
dc.identifier.other WOS:000797308000003
dc.identifier.startpage 7521 en_US
dc.identifier.uri https://doi.org/10.1007/s11033-022-07560-5
dc.identifier.uri https://hdl.handle.net/20.500.12573/1476
dc.identifier.volume 49 en_US
dc.language.iso eng en_US
dc.publisher SPRINGER en_US
dc.relation.isversionof 10.1007/s11033-022-07560-5 en_US
dc.relation.journal MOLECULAR BIOLOGY REPORTS en_US
dc.relation.publicationcategory Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı en_US
dc.rights info:eu-repo/semantics/closedAccess en_US
dc.subject Cancer en_US
dc.subject Ethacrynic acid en_US
dc.subject Cinnamic acid en_US
dc.subject Combination therapy en_US
dc.subject Apoptosis en_US
dc.subject Cell cycle en_US
dc.title Ethacrynic acid and cinnamic acid combination exhibits selective anticancer effects on K562 chronic myeloid leukemia cells en_US
dc.type article en_US

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