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Article

Daidzein inhibits choriocarcinoma proliferation by arresting cell cycle at G1 phase through suppressing ERK pathway in vitro and in vivo

  • Authors:
    • Wei Zheng
    • Rong Sun
    • Lei Yang
    • Xianling Zeng
    • Yan Xue
    • Ruifang An
  • View Affiliations / Copyright

    Affiliations: Department of Gynecology and Obstetrics, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, Shaanxi 710061, P.R. China, Obstetrics and Gynecology Hospital, Fudan University, Shanghai 200012, P.R. China
  • Pages: 2518-2524
    |
    Published online on: August 28, 2017
       https://doi.org/10.3892/or.2017.5928
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Abstract

Choriocarcinoma is a highly malignant tumor arising from abnormal gestational trophoblast proliferation. Although chemotherapy has dramatically improved the prognosis, there are still some patients who become drug-resistant or relapse. Daidzein has garnered interest in its antitumor activity especially in proliferation inhibition. However, few reports exist on daidzein effect in growth of choriocarcinoma. Therefore, in this study, we performed in vitro and in vivo experiment in JAR and JEG‑3 to investigate the effect of daidzein in proliferation of choriocarcinoma. Daidzein inhibited cell growth in a time- and dose-dependent way. Cell cycle was arrested at G1 phase and expression of cyclin D1, c-myc, PCNA was reduced while p21 was upregulated during daidzein treatment. At the same time, the expression of p-ERK was downregulated and translocation into nuclear afterwards was also inhibited. Moreover, ERK agonist ceramide C6 abolished daidzein's effects on cell proliferation. Besides, in vivo experiment also showed daidzein's anti-proliferation function as xenografts growth was inhibited and expressions of c-myc, PCNA and p-ERK were suppressed. In conclusion, results in our study demonstrate daidzein can inhibit choriocarcinoma cell proliferation in vitro and in vivo; underlying mechanism behind the inhibitory effects may probably be suppressing ERK pathway and afterwards arresting cell cycle at G1 phase.
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Copy and paste a formatted citation
Spandidos Publications style
Zheng W, Sun R, Yang L, Zeng X, Xue Y and An R: Daidzein inhibits choriocarcinoma proliferation by arresting cell cycle at G1 phase through suppressing ERK pathway in vitro and in vivo. Oncol Rep 38: 2518-2524, 2017.
APA
Zheng, W., Sun, R., Yang, L., Zeng, X., Xue, Y., & An, R. (2017). Daidzein inhibits choriocarcinoma proliferation by arresting cell cycle at G1 phase through suppressing ERK pathway in vitro and in vivo. Oncology Reports, 38, 2518-2524. https://doi.org/10.3892/or.2017.5928
MLA
Zheng, W., Sun, R., Yang, L., Zeng, X., Xue, Y., An, R."Daidzein inhibits choriocarcinoma proliferation by arresting cell cycle at G1 phase through suppressing ERK pathway in vitro and in vivo". Oncology Reports 38.4 (2017): 2518-2524.
Chicago
Zheng, W., Sun, R., Yang, L., Zeng, X., Xue, Y., An, R."Daidzein inhibits choriocarcinoma proliferation by arresting cell cycle at G1 phase through suppressing ERK pathway in vitro and in vivo". Oncology Reports 38, no. 4 (2017): 2518-2524. https://doi.org/10.3892/or.2017.5928
Copy and paste a formatted citation
x
Spandidos Publications style
Zheng W, Sun R, Yang L, Zeng X, Xue Y and An R: Daidzein inhibits choriocarcinoma proliferation by arresting cell cycle at G1 phase through suppressing ERK pathway in vitro and in vivo. Oncol Rep 38: 2518-2524, 2017.
APA
Zheng, W., Sun, R., Yang, L., Zeng, X., Xue, Y., & An, R. (2017). Daidzein inhibits choriocarcinoma proliferation by arresting cell cycle at G1 phase through suppressing ERK pathway in vitro and in vivo. Oncology Reports, 38, 2518-2524. https://doi.org/10.3892/or.2017.5928
MLA
Zheng, W., Sun, R., Yang, L., Zeng, X., Xue, Y., An, R."Daidzein inhibits choriocarcinoma proliferation by arresting cell cycle at G1 phase through suppressing ERK pathway in vitro and in vivo". Oncology Reports 38.4 (2017): 2518-2524.
Chicago
Zheng, W., Sun, R., Yang, L., Zeng, X., Xue, Y., An, R."Daidzein inhibits choriocarcinoma proliferation by arresting cell cycle at G1 phase through suppressing ERK pathway in vitro and in vivo". Oncology Reports 38, no. 4 (2017): 2518-2524. https://doi.org/10.3892/or.2017.5928
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