The Mechanism of the Synergistic Anticancer Effect of CDDP and EPA in the TE1 Cell Line
Autor: | Ayako Ogo, Masaharu Higashida, Hideo Matsumoto, Hisako Kubota, Toshihiro Hirai, Tomio Ueno, Fusako Teramoto, Sachi Miyake |
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Rok vydání: | 2021 |
Předmět: |
inorganic chemicals
Cancer Research Cell cycle checkpoint Esophageal Neoplasms medicine.medical_treatment Apoptosis Flow cytometry Cell Line Tumor Antineoplastic Combined Chemotherapy Protocols medicine Humans neoplasms health care economics and organizations Unsaturated fatty acid Cisplatin medicine.diagnostic_test Chemistry Interleukin-6 NF-kappa B Drug Synergism General Medicine Cell cycle Eicosapentaenoic acid female genital diseases and pregnancy complications G2 Phase Cell Cycle Checkpoints Cytokine Oncology Eicosapentaenoic Acid S Phase Cell Cycle Checkpoints Cancer research lipids (amino acids peptides and proteins) medicine.drug Signal Transduction |
Zdroj: | Anticancer research. 41(4) |
ISSN: | 1791-7530 |
Popis: | Background/aim Eicosapentaenoic acid (EPA) is an unsaturated fatty acid with various bioactivities, including antitumor effects. We previously reported a synergistic antitumor effect of cisplatin (CDDP) and EPA. Here, we examined the underlying mechanism. Materials and methods The human oesophageal cancer cell line TE-1 was treated with the combination of EPA and CDDP. Nuclear translocation of NF-κB, a transcription factor involved in cytokine production, was detected by immunohistochemistry. IL-6 levels were measured by ELISA. Apoptosis and cell cycle distribution were evaluated by flow cytometry. Results Nuclear translocation of NF-κB in TE-1 cells was synergistically decreased by CDDP and EPA. IL-6 production was increased following treatment with CDDP, but treatment with EPA decreased IL-6 levels. Apoptosis was synergistically induced by CDDP and EPA. A G2/M cell cycle arrest was observed with the combination of CDDP and 150 μM EPA, and S phase arrest with the combination of CDDP and 100 μM EPA. Conclusion The combination of CDDP and EPA synergistically suppresses NF-κB nuclear translocation and increases apoptosis by inducing cell cycle arrest at the S or G2/M phase. |
Databáze: | OpenAIRE |
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