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Article

MEK inhibitor, PD98059, promotes breast cancer cell migration by inducing β-catenin nuclear accumulation

  • Authors:
    • Ying Zhao
    • Chao-Chao Ge
    • Jun Wang
    • Xiao-Xiao Wu
    • Xiao-Min Li
    • Wei Li
    • Sha-Sha Wang
    • Tong Liu
    • Jiu-Zhou Hou
    • Hua Sun
    • Dong Fang
    • Song-Qiang Xie
  • View Affiliations / Copyright

    Affiliations: Institute of Chemical Biology, College of Pharmacy, Henan University, Kaifeng, Henan 475004, P.R. China
  • Pages: 3055-3063
    |
    Published online on: September 13, 2017
       https://doi.org/10.3892/or.2017.5955
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Abstract

Abnormal activation of the RAF/MEK/ERK signaling pathway has been observed in breast cancer. Thus, a number of MEK inhibitors have been designed as one treatment option for breast cancer. Although some studies have found that these MEK inhibitors inhibit the growth of a variety of human cancer cells, some trials have shown that the use of MEK inhibitors as a treatment for breast cancer does not adequately improve survival for unknown reasons. In the present study, MEK inhibitor PD98059 was used to evaluate its anticancer effects on human breast cancer MCF-7 and MDA-MB-231 cells and to explore the possible mechanism of action. Our results revealed that MEK inhibitor PD98059 exhibited antiproliferative effects in a dose- and time-dependent manner in MCF-7 and MDA-MB-231 breast cancer cells. Conversely, incubation of MCF-7 and MDA-MB-231 cells with PD98059 promoted their migration. Further investigation disclosed that the enhanced ability of migration promoted by PD98059 was dependent on β-catenin nuclear translocation in the MCF-7 and MDA-MB‑231 cells. Subsequent experiments documented that activation of EGFR signaling induced by PD98059 increased the amount of β-catenin in the nucleus. Taken together, our findings may elucidate a possible mechanism explaining the ineffectiveness of MEK inhibitors in breast cancer treatment and improve our understanding of the role of MEK in cancer.
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Copy and paste a formatted citation
Spandidos Publications style
Zhao Y, Ge C, Wang J, Wu X, Li X, Li W, Wang S, Liu T, Hou J, Sun H, Sun H, et al: MEK inhibitor, PD98059, promotes breast cancer cell migration by inducing β-catenin nuclear accumulation. Oncol Rep 38: 3055-3063, 2017.
APA
Zhao, Y., Ge, C., Wang, J., Wu, X., Li, X., Li, W. ... Xie, S. (2017). MEK inhibitor, PD98059, promotes breast cancer cell migration by inducing β-catenin nuclear accumulation. Oncology Reports, 38, 3055-3063. https://doi.org/10.3892/or.2017.5955
MLA
Zhao, Y., Ge, C., Wang, J., Wu, X., Li, X., Li, W., Wang, S., Liu, T., Hou, J., Sun, H., Fang, D., Xie, S."MEK inhibitor, PD98059, promotes breast cancer cell migration by inducing β-catenin nuclear accumulation". Oncology Reports 38.5 (2017): 3055-3063.
Chicago
Zhao, Y., Ge, C., Wang, J., Wu, X., Li, X., Li, W., Wang, S., Liu, T., Hou, J., Sun, H., Fang, D., Xie, S."MEK inhibitor, PD98059, promotes breast cancer cell migration by inducing β-catenin nuclear accumulation". Oncology Reports 38, no. 5 (2017): 3055-3063. https://doi.org/10.3892/or.2017.5955
Copy and paste a formatted citation
x
Spandidos Publications style
Zhao Y, Ge C, Wang J, Wu X, Li X, Li W, Wang S, Liu T, Hou J, Sun H, Sun H, et al: MEK inhibitor, PD98059, promotes breast cancer cell migration by inducing β-catenin nuclear accumulation. Oncol Rep 38: 3055-3063, 2017.
APA
Zhao, Y., Ge, C., Wang, J., Wu, X., Li, X., Li, W. ... Xie, S. (2017). MEK inhibitor, PD98059, promotes breast cancer cell migration by inducing β-catenin nuclear accumulation. Oncology Reports, 38, 3055-3063. https://doi.org/10.3892/or.2017.5955
MLA
Zhao, Y., Ge, C., Wang, J., Wu, X., Li, X., Li, W., Wang, S., Liu, T., Hou, J., Sun, H., Fang, D., Xie, S."MEK inhibitor, PD98059, promotes breast cancer cell migration by inducing β-catenin nuclear accumulation". Oncology Reports 38.5 (2017): 3055-3063.
Chicago
Zhao, Y., Ge, C., Wang, J., Wu, X., Li, X., Li, W., Wang, S., Liu, T., Hou, J., Sun, H., Fang, D., Xie, S."MEK inhibitor, PD98059, promotes breast cancer cell migration by inducing β-catenin nuclear accumulation". Oncology Reports 38, no. 5 (2017): 3055-3063. https://doi.org/10.3892/or.2017.5955
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