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• W2891904697 abstract "Resistance to 5‑fluorouracil (5‑FU) is a serious problem in cancer therapy and overcoming it is required in order to improve the efficacy of cancer chemotherapy. Histone deacetylase (HDAC) inhibitors are used in cancer treatments and, recently, it has been reported that HDAC inhibitors can overcome resistance to various anti‑cancer drugs in vitro. In the present study, a 5‑FU‑resistant breast cancer cell line was established, and the effects of HDAC inhibitors in these cells were examined. The 5‑FU‑resistant cell line MDA‑MB‑468 (MDA468/FU) was established by continuous exposure of the parental cells to 5‑FU. This subline was characterized by high resistance to 5‑FU, higher mRNA expression levels of thymidylate synthetase and dihydropyrimidine dehydrogenase (DPD), and lower mRNA expression levels of uridine monophosphate synthetase (UMPS) than the parental cells. Gimeracil, a DPD inhibitor, did not affect the sensitivity of MDA468/FU cells to 5‑FU. Oteracil, a UMPS inhibitor, decreased the cytotoxicity of 5‑FU in MDA468 cells, but not in MDA468/FU cells. The HDAC inhibitors, valproic acid and suberanilohydroxamic acid sensitized the two cell lines to 5‑FU in a concentration‑dependent manner. In conclusion, the results of the present study revealed that HDAC inhibitors increase the sensitivity to 5‑FU in 5‑FU‑sensitive and ‑resistant cells." @default.
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• W2891904697 date "2018-09-04" @default.
• W2891904697 modified "2023-10-03" @default.
• W2891904697 title "Histone deacetylase inhibitors sensitize 5‑fluorouracil‑resistant MDA‑MB‑468 breast cancer cells to 5‑fluorouracil" @default.
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• W2891904697 doi "https://doi.org/10.3892/ol.2018.9388" @default.
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