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Article

Tetramethylpyrazine reduces prostate cancer malignancy through inactivation of the DPP10‑AS1/CBP/FOXM1 signaling pathway

  • Authors:
    • Yi Zhou
    • Zhien Zhou
    • Zhigang Ji
    • Weigang Yan
    • Hanzhong Li
    • Xiao Yu
  • View Affiliations / Copyright

    Affiliations: Department of Urology, Peking Union Medical College Hospital, Chinese Academy of Medical Science and Peking Union Medical College, Beijing 100000, P.R. China, Department of Pathology, Peking Union Medical College Hospital, Chinese Academy of Medical Science and Peking Union Medical College, Beijing 100000, P.R. China
  • Pages: 314-324
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    Published online on: April 1, 2020
       https://doi.org/10.3892/ijo.2020.5036
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Abstract

Tetramethylpyrazine (TMP), a Chinese herbal medicine, has been reported to possess anticancer effects. Emerging evidence suggests that various long noncoding RNAs (lncRNAs) serve important roles in cancer initiation and progression. In the present study, the tumor‑suppressive effects of TMP in human PCa cells was examined and the underlying mechanisms of its actions were determined. The data showed that TMP treatment reduced cell viability and increased apoptosis in a dose‑dependent manner. Reverse transcription‑quantitative PCR showed TMP treatment increased the expression of lncRNA DPP10‑AS1 in PCa cells. Furthermore, DPP10‑AS1 was also upregulated in TMP‑resistant PCa cells. Knockdown of DPP10‑AS1 reversed TMP resistance, whereas increased expression of DPP10‑AS1 abrogated the TMP‑mediated cytotoxicity in PCa cells. In addition, forkhead box M1 (FOXM1) was verified as the functional target of DPP10‑AS1, and knockdown of FOXM1 reversed the TMP/DPP10‑AS1‑induced cell cytotoxicity. Mechanistically, DPP10‑AS1 was associated with CREB binding protein, thereby induced H3K27ac enrichment at the promoter region of the FOXM1 gene. In conclusion, the present study showed that TMP may be a promising treatment agent for PCa and lncRNA DPP10‑AS1 may be a promising therapeutic target for TMP treatment.
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Copy and paste a formatted citation
Spandidos Publications style
Zhou Y, Zhou Z, Ji Z, Yan W, Li H and Yu X: Tetramethylpyrazine reduces prostate cancer malignancy through inactivation of the DPP10‑AS1/CBP/FOXM1 signaling pathway. Int J Oncol 57: 314-324, 2020.
APA
Zhou, Y., Zhou, Z., Ji, Z., Yan, W., Li, H., & Yu, X. (2020). Tetramethylpyrazine reduces prostate cancer malignancy through inactivation of the DPP10‑AS1/CBP/FOXM1 signaling pathway. International Journal of Oncology, 57, 314-324. https://doi.org/10.3892/ijo.2020.5036
MLA
Zhou, Y., Zhou, Z., Ji, Z., Yan, W., Li, H., Yu, X."Tetramethylpyrazine reduces prostate cancer malignancy through inactivation of the DPP10‑AS1/CBP/FOXM1 signaling pathway". International Journal of Oncology 57.1 (2020): 314-324.
Chicago
Zhou, Y., Zhou, Z., Ji, Z., Yan, W., Li, H., Yu, X."Tetramethylpyrazine reduces prostate cancer malignancy through inactivation of the DPP10‑AS1/CBP/FOXM1 signaling pathway". International Journal of Oncology 57, no. 1 (2020): 314-324. https://doi.org/10.3892/ijo.2020.5036
Copy and paste a formatted citation
x
Spandidos Publications style
Zhou Y, Zhou Z, Ji Z, Yan W, Li H and Yu X: Tetramethylpyrazine reduces prostate cancer malignancy through inactivation of the DPP10‑AS1/CBP/FOXM1 signaling pathway. Int J Oncol 57: 314-324, 2020.
APA
Zhou, Y., Zhou, Z., Ji, Z., Yan, W., Li, H., & Yu, X. (2020). Tetramethylpyrazine reduces prostate cancer malignancy through inactivation of the DPP10‑AS1/CBP/FOXM1 signaling pathway. International Journal of Oncology, 57, 314-324. https://doi.org/10.3892/ijo.2020.5036
MLA
Zhou, Y., Zhou, Z., Ji, Z., Yan, W., Li, H., Yu, X."Tetramethylpyrazine reduces prostate cancer malignancy through inactivation of the DPP10‑AS1/CBP/FOXM1 signaling pathway". International Journal of Oncology 57.1 (2020): 314-324.
Chicago
Zhou, Y., Zhou, Z., Ji, Z., Yan, W., Li, H., Yu, X."Tetramethylpyrazine reduces prostate cancer malignancy through inactivation of the DPP10‑AS1/CBP/FOXM1 signaling pathway". International Journal of Oncology 57, no. 1 (2020): 314-324. https://doi.org/10.3892/ijo.2020.5036
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