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MicroRNA‑34b expression enhances chemosensitivity of endometrial cancer cells to paclitaxel

  • Authors:
    • Megumi Yanokura
    • Kouji Banno
    • Daisuke Aoki
  • View Affiliations / Copyright

    Affiliations: Department of Obstetrics and Gynecology, Keio University School of Medicine, Tokyo 160‑8582, Japan
    Copyright: © Yanokura et al. This is an open access article distributed under the terms of Creative Commons Attribution License.
  • Pages: 1145-1156
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    Published online on: September 23, 2020
       https://doi.org/10.3892/ijo.2020.5127
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Abstract

Aberrant DNA methylation is widely observed in various types of cancer, and expression of microRNAs (miRNAs/miRs) is suppressed by DNA methylation. The present study explored tumor suppressor miRNAs downregulated by DNA methylation in endometrial cancer cells, as the basis of a novel therapeutic approach for endometrial cancer. Among 821 candidate miRNAs, miR‑34b was identified as an upregulated miRNA after demethylation treatment in all four endometrial cancer cell lines (HEC‑108, SNG‑II, Ishikawa and HHUA) examined. miR‑34b expression with or without demethylation treatment in cancer cells was confirmed by TaqMan quantitative PCR. MYC and MET, the predicted target genes of miR‑34b, were downregulated at both the RNA and protein levels following miR‑34b overexpression. Following miR‑34b treatment, inhibition of cell growth and invasion, and cell cycle arrest were observed in HEC‑108 cells. Sensitivity to paclitaxel was increased in cancer cells with miR‑34b overexpression, compared with untreated cancer cells, but this difference was not identified for cisplatin or doxorubicin. In vivo, combination treatment with miR‑34b and paclitaxel markedly reduced tumor growth compared with treatment with negative control miRNA and paclitaxel. These data suggest that miR‑34b enhances paclitaxel sensitivity in endometrial cancer cells, and that miR‑34b and MET are key targets for treatment of endometrial cancer. The present results may contribute to the development of combination treatment with a demethylation agent, miR‑34b mimic or MET inhibitor and an anticancer drug.
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Copy and paste a formatted citation
Spandidos Publications style
Yanokura M, Banno K and Aoki D: MicroRNA‑34b expression enhances chemosensitivity of endometrial cancer cells to paclitaxel. Int J Oncol 57: 1145-1156, 2020.
APA
Yanokura, M., Banno, K., & Aoki, D. (2020). MicroRNA‑34b expression enhances chemosensitivity of endometrial cancer cells to paclitaxel. International Journal of Oncology, 57, 1145-1156. https://doi.org/10.3892/ijo.2020.5127
MLA
Yanokura, M., Banno, K., Aoki, D."MicroRNA‑34b expression enhances chemosensitivity of endometrial cancer cells to paclitaxel". International Journal of Oncology 57.5 (2020): 1145-1156.
Chicago
Yanokura, M., Banno, K., Aoki, D."MicroRNA‑34b expression enhances chemosensitivity of endometrial cancer cells to paclitaxel". International Journal of Oncology 57, no. 5 (2020): 1145-1156. https://doi.org/10.3892/ijo.2020.5127
Copy and paste a formatted citation
x
Spandidos Publications style
Yanokura M, Banno K and Aoki D: MicroRNA‑34b expression enhances chemosensitivity of endometrial cancer cells to paclitaxel. Int J Oncol 57: 1145-1156, 2020.
APA
Yanokura, M., Banno, K., & Aoki, D. (2020). MicroRNA‑34b expression enhances chemosensitivity of endometrial cancer cells to paclitaxel. International Journal of Oncology, 57, 1145-1156. https://doi.org/10.3892/ijo.2020.5127
MLA
Yanokura, M., Banno, K., Aoki, D."MicroRNA‑34b expression enhances chemosensitivity of endometrial cancer cells to paclitaxel". International Journal of Oncology 57.5 (2020): 1145-1156.
Chicago
Yanokura, M., Banno, K., Aoki, D."MicroRNA‑34b expression enhances chemosensitivity of endometrial cancer cells to paclitaxel". International Journal of Oncology 57, no. 5 (2020): 1145-1156. https://doi.org/10.3892/ijo.2020.5127
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