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Ginsenoside Rg3 inhibits the migration and invasion of liver cancer cells by increasing the protein expression of ARHGAP9

  • Authors:
    • Meng‑Yao Sun
    • Ya‑Nan Song
    • Miao Zhang
    • Chun‑Yan Zhang
    • Li‑Jun Zhang
    • Hong Zhang
  • View Affiliations / Copyright

    Affiliations: Department of Pharmaceutical Botany, School of Pharmacy, Second Military Medical University, Shanghai 200433, P.R. China, Central Laboratory, Seventh People's Hospital of Shanghai University of Traditional Chinese Medicine, Shanghai 200137, P.R. China
    Copyright: © Sun et al. This is an open access article distributed under the terms of Creative Commons Attribution License.
  • Pages: 965-973
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    Published online on: November 15, 2018
       https://doi.org/10.3892/ol.2018.9701
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Abstract

Ginsenoside Rg3, a naturally occurring phytochemical, serves an important role in the prevention and treatment of cancer. In the present study, with the aim to reveal the molecular mechanism of Rg3 in liver cancer cell metastasis, the anti‑migration and anti‑invasion effects of Rg3 on liver cancer cells were investigated. It was demonstrated that Rg3 caused marked inhibition of cell migration and invasion of human liver cancer cells, HepG2 and MHCC‑97L, in vitro, and the growth of HepG2 and MHCC‑97L tumors in BABL/c nude mice. The protein expression of Rho GTPase activating protein 9 (ARHGAP9) was increased both in HepG2 and MHCC‑97L cells. Following ARHGAP9 knockdown, the results of Transwell and tumorigenesis assays revealed that the anti‑migration, anti‑invasion and anti‑tumor growth effects of Rg3 were impaired significantly. The increased expression of ARHGAP9 protein induced by Rg3 was remarkably suppressed. All results suggested that ARHGAP9 protein may be a vital regulator in the anti‑metastatic role of Rg3. To the best of our knowledge, the present study is the first to report that Rg3 effectively suppressed the migration and invasion of liver cancer cells by upregulating the protein expression of ARHGAP9, indicating a novel natural therapeutic agent and a therapeutic target for the treatment of liver cancer.
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Copy and paste a formatted citation
Spandidos Publications style
Sun MY, Song YN, Zhang M, Zhang CY, Zhang LJ and Zhang H: Ginsenoside Rg3 inhibits the migration and invasion of liver cancer cells by increasing the protein expression of ARHGAP9. Oncol Lett 17: 965-973, 2019.
APA
Sun, M., Song, Y., Zhang, M., Zhang, C., Zhang, L., & Zhang, H. (2019). Ginsenoside Rg3 inhibits the migration and invasion of liver cancer cells by increasing the protein expression of ARHGAP9. Oncology Letters, 17, 965-973. https://doi.org/10.3892/ol.2018.9701
MLA
Sun, M., Song, Y., Zhang, M., Zhang, C., Zhang, L., Zhang, H."Ginsenoside Rg3 inhibits the migration and invasion of liver cancer cells by increasing the protein expression of ARHGAP9". Oncology Letters 17.1 (2019): 965-973.
Chicago
Sun, M., Song, Y., Zhang, M., Zhang, C., Zhang, L., Zhang, H."Ginsenoside Rg3 inhibits the migration and invasion of liver cancer cells by increasing the protein expression of ARHGAP9". Oncology Letters 17, no. 1 (2019): 965-973. https://doi.org/10.3892/ol.2018.9701
Copy and paste a formatted citation
x
Spandidos Publications style
Sun MY, Song YN, Zhang M, Zhang CY, Zhang LJ and Zhang H: Ginsenoside Rg3 inhibits the migration and invasion of liver cancer cells by increasing the protein expression of ARHGAP9. Oncol Lett 17: 965-973, 2019.
APA
Sun, M., Song, Y., Zhang, M., Zhang, C., Zhang, L., & Zhang, H. (2019). Ginsenoside Rg3 inhibits the migration and invasion of liver cancer cells by increasing the protein expression of ARHGAP9. Oncology Letters, 17, 965-973. https://doi.org/10.3892/ol.2018.9701
MLA
Sun, M., Song, Y., Zhang, M., Zhang, C., Zhang, L., Zhang, H."Ginsenoside Rg3 inhibits the migration and invasion of liver cancer cells by increasing the protein expression of ARHGAP9". Oncology Letters 17.1 (2019): 965-973.
Chicago
Sun, M., Song, Y., Zhang, M., Zhang, C., Zhang, L., Zhang, H."Ginsenoside Rg3 inhibits the migration and invasion of liver cancer cells by increasing the protein expression of ARHGAP9". Oncology Letters 17, no. 1 (2019): 965-973. https://doi.org/10.3892/ol.2018.9701
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