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Article

The restraining effect of baicalein and U0126 on human cervical cancer cell line HeLa

  • Authors:
    • Haiqiong Ye
    • Yujiao Zhang
    • Yongzhou Wang
    • Jiyi Xia
    • Xiguang Mao
    • Xiaolan Yu
  • View Affiliations / Copyright

    Affiliations: Department of Obstetrics and Gynecology, The Affiliated Hospital of Southwest Medical University, Luzhou, Sichuan 646000, P.R. China, Department of Obstetrics and Gynecology, The Affiliated Traditional Chinese Medicine Hospital of Southwest Medical University, Luzhou, Sichuan 646000, P.R. China, School of Medical Information and Engineering, Southwest Medical University, Luzhou, Sichuan 646000, P.R. China
  • Pages: 957-963
    |
    Published online on: May 30, 2017
       https://doi.org/10.3892/mmr.2017.6648
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Abstract

To explore the restraining effect of baicalein and the mitogen-activation protein kinase kinase inhibitor, U0126, on human cervical cell line HeLa proliferation, apoptosis and migration. HeLa cells were treated by different concentrations of baicalein or U0126. A Cell Counting Kit (CCK)‑8 assay was applied to examine cell viability. Flow cytometry was used to determine cell cycle and apoptosis. A wound healing assay was performed to detect cell migration. A terminal deoxynucleotidyl transferase dUTP nick end labeling assay was adopted to test cell apoptosis. Reverse transcription‑quantitative polymerase chain reaction and western blot analysis was used to detect apoptosis gene and protein expression. CCK‑8 assay demonstrated that baicalein and U0126 suppressed HeLa cell viability by dose dependence. TUNEL, Annexin V‑fluorescein isothiocyanate/propidium iodide, and ratio of Bcl‑2‑associated X protein and B cell lymphoma 2 indicated that baicalein and U0126 induced HeLa cell apoptosis. Flow cytometry revealed that baicalein blocked the cell cycle of HeLa in G0/G1 phase. A wound healing assay demonstrated that baicalein significantly inhibited HeLa cell migration compared with control. Baicalein and U0126 markedly downregulated extracellular signal‑regulated kinase 1/2, matrix metalloproteinase (MMP) 2 and MMP9 levels both in mRNA and protein. In the present study, the authors demonstrated that baicalein and U0126 may be used in cervical cancer treatment by inhibiting cell migration and inducing cell apoptosis.
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Copy and paste a formatted citation
Spandidos Publications style
Ye H, Zhang Y, Wang Y, Xia J, Mao X and Yu X: The restraining effect of baicalein and U0126 on human cervical cancer cell line HeLa. Mol Med Rep 16: 957-963, 2017.
APA
Ye, H., Zhang, Y., Wang, Y., Xia, J., Mao, X., & Yu, X. (2017). The restraining effect of baicalein and U0126 on human cervical cancer cell line HeLa. Molecular Medicine Reports, 16, 957-963. https://doi.org/10.3892/mmr.2017.6648
MLA
Ye, H., Zhang, Y., Wang, Y., Xia, J., Mao, X., Yu, X."The restraining effect of baicalein and U0126 on human cervical cancer cell line HeLa". Molecular Medicine Reports 16.1 (2017): 957-963.
Chicago
Ye, H., Zhang, Y., Wang, Y., Xia, J., Mao, X., Yu, X."The restraining effect of baicalein and U0126 on human cervical cancer cell line HeLa". Molecular Medicine Reports 16, no. 1 (2017): 957-963. https://doi.org/10.3892/mmr.2017.6648
Copy and paste a formatted citation
x
Spandidos Publications style
Ye H, Zhang Y, Wang Y, Xia J, Mao X and Yu X: The restraining effect of baicalein and U0126 on human cervical cancer cell line HeLa. Mol Med Rep 16: 957-963, 2017.
APA
Ye, H., Zhang, Y., Wang, Y., Xia, J., Mao, X., & Yu, X. (2017). The restraining effect of baicalein and U0126 on human cervical cancer cell line HeLa. Molecular Medicine Reports, 16, 957-963. https://doi.org/10.3892/mmr.2017.6648
MLA
Ye, H., Zhang, Y., Wang, Y., Xia, J., Mao, X., Yu, X."The restraining effect of baicalein and U0126 on human cervical cancer cell line HeLa". Molecular Medicine Reports 16.1 (2017): 957-963.
Chicago
Ye, H., Zhang, Y., Wang, Y., Xia, J., Mao, X., Yu, X."The restraining effect of baicalein and U0126 on human cervical cancer cell line HeLa". Molecular Medicine Reports 16, no. 1 (2017): 957-963. https://doi.org/10.3892/mmr.2017.6648
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