Induction of autophagic cell death by thymoquinone in docetaxel resistant prostate cancer cells; [Dosetaksel dirençli prostat kanseri hücrelerinde timokinon tarafından otofajik hücre ölümünün indüklenmesi]
dc.contributor.author | İlhan S. | |
dc.contributor.author | Oğuz F. | |
dc.date.accessioned | 2024-07-22T08:06:40Z | |
dc.date.available | 2024-07-22T08:06:40Z | |
dc.date.issued | 2021 | |
dc.description.abstract | Aim: Acquired docetaxel (DOC) resistance of prostate cancer (PCa) is still a clinical problem. In addition to failure in chemotherapy treatment, it causes tumor recurrence. Therefore, novel and more effective compounds are needed in DOC-resistant PCa treatment. This study aimed to investigate the possible cytotoxic and cell death-inducing activities of thymoquinone (TQ), one of the main active components of Nigella sativa L., on DOC-resistant prostate cancer cells. Material and Methods: DOC-resistant PC3 cells (DOC-R/PC3) were developed by the continuous culture with increment concentrations of DOC (1-10 nM) until they improved their growth and division abilities. The cell viability was determined by MTT assay. The Muse™ Annexin V & Dead Cell kit was performed to detect apoptotic cell death. Autophagic vacuoles were observed by staining autophagic vacuoles. The levels of LC3I, LC3II and Beclin-1 proteins were investigated via western blot analysis. Results: TQ inhibited the viability of DOC-R/PC3 cells in a dose-and time-dependent manner (p=0.014). The IC50 value of TQ for DOC-R/PC3 cells was calculated as 60 µM at 72 h. Treatment of TQ did not induce apoptotic cell death in DOC-resistant prostate cancer cells but induced the formation of autophagic vacuoles. Moreover, Beclin-1 and LC3-II protein levels were increased in TQ-treated DOC-R/PC3 cells, however, LC3-I levels were decreased in DOC-R/PC3 cells. Conclusion: All these results show that TQ may become a new therapeutic target for DOC-resistant prostate cancer in the future. © 2021, Duzce University Medical School. All rights reserved. | |
dc.identifier.DOI-ID | 10.18678/dtfd.925238 | |
dc.identifier.issn | 1307671X | |
dc.identifier.uri | http://akademikarsiv.cbu.edu.tr:4000/handle/123456789/13656 | |
dc.language.iso | English | |
dc.publisher | Duzce University Medical School | |
dc.rights | All Open Access; Gold Open Access; Green Open Access | |
dc.subject | docetaxel | |
dc.subject | glutamine | |
dc.subject | nefopam | |
dc.subject | phosphatidylserine | |
dc.subject | streptomycin | |
dc.subject | thymoquinone | |
dc.subject | apoptosis | |
dc.subject | Article | |
dc.subject | autophagic cell death | |
dc.subject | cell viability | |
dc.subject | cytotoxicity | |
dc.subject | fetal bovine serum | |
dc.subject | human | |
dc.subject | human cell | |
dc.subject | prostate cancer | |
dc.subject | prostate cancer cell line | |
dc.subject | protein expression | |
dc.subject | tumor recurrence | |
dc.subject | Western blotting | |
dc.title | Induction of autophagic cell death by thymoquinone in docetaxel resistant prostate cancer cells; [Dosetaksel dirençli prostat kanseri hücrelerinde timokinon tarafından otofajik hücre ölümünün indüklenmesi] | |
dc.type | Article |