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The anti‑migration and anti‑invasion effects of Bruceine D in human triple‑negative breast cancer MDA‑MB‑231 cells

  • Authors:
    • Can Luo
    • Yu Wang
    • Cheng Wei
    • Yuxin Chen
    • Zhaoning Ji
  • View Affiliations / Copyright

    Affiliations: Department of Oncology, Yijishan Hospital of Wannan Medical College, Wuhu, Anhui 241001, P.R. China, Department of Oncology, Wannan Medical College, Wuhu, Anhui 241001, P.R. China, Department of Oncology, Gaoyou People's Hospital, Gaoyou Hospital Affiliated to Soochow University, Gaoyou, Jiangsu 225600, P.R. China
    Copyright: © Luo et al. This is an open access article distributed under the terms of Creative Commons Attribution License.
  • Pages: 273-279
    |
    Published online on: November 12, 2019
       https://doi.org/10.3892/etm.2019.8187
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Abstract

Brucein D (BD) is a naturally occurring major active quassinoid extracted from the Chinese medicinal herb Brucea javanica, which has been previously demonstrated to exhibit anticancer activities. The present study aimed to investigate the anticancer effects of BD on MDA‑MB‑231 cells, a human triple‑negative breast cancer (TNBC) cell line. An MTT assay was performed to assess cell viability, whilst wound healing and Transwell assay were applied to measure cell migration and invasion, respectively. Western blot analysis was performed to assess the expression of E‑cadherin, vimentin and β‑catenin, which are proteins associated with epithelial‑mesenchymal transformation (EMT), and PI3K, AKT and p‑AKT, which are key components of the PI3K/AKT signaling pathway. BD was indicated to reduce cell viability in a dose‑ and time‑dependent manner, whilst cell invasion and migration were also significantly inhibited in a dose‑dependent manner. Western blot analysis demonstrated that BD treatment significantly upregulated the expression of E‑cadherin and downregulated the expression of vimentin and β‑catenin. Additionally, BD downregulated the expression of PI3K and reduced AKT phosphorylation. In conclusion, BD can inhibit MDA‑MB‑231 cell viability, migration and invasion, suggesting the potential use of BD for the treatment of TNBC.
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Copy and paste a formatted citation
Spandidos Publications style
Luo C, Wang Y, Wei C, Chen Y and Ji Z: The anti‑migration and anti‑invasion effects of Bruceine D in human triple‑negative breast cancer MDA‑MB‑231 cells. Exp Ther Med 19: 273-279, 2020.
APA
Luo, C., Wang, Y., Wei, C., Chen, Y., & Ji, Z. (2020). The anti‑migration and anti‑invasion effects of Bruceine D in human triple‑negative breast cancer MDA‑MB‑231 cells. Experimental and Therapeutic Medicine, 19, 273-279. https://doi.org/10.3892/etm.2019.8187
MLA
Luo, C., Wang, Y., Wei, C., Chen, Y., Ji, Z."The anti‑migration and anti‑invasion effects of Bruceine D in human triple‑negative breast cancer MDA‑MB‑231 cells". Experimental and Therapeutic Medicine 19.1 (2020): 273-279.
Chicago
Luo, C., Wang, Y., Wei, C., Chen, Y., Ji, Z."The anti‑migration and anti‑invasion effects of Bruceine D in human triple‑negative breast cancer MDA‑MB‑231 cells". Experimental and Therapeutic Medicine 19, no. 1 (2020): 273-279. https://doi.org/10.3892/etm.2019.8187
Copy and paste a formatted citation
x
Spandidos Publications style
Luo C, Wang Y, Wei C, Chen Y and Ji Z: The anti‑migration and anti‑invasion effects of Bruceine D in human triple‑negative breast cancer MDA‑MB‑231 cells. Exp Ther Med 19: 273-279, 2020.
APA
Luo, C., Wang, Y., Wei, C., Chen, Y., & Ji, Z. (2020). The anti‑migration and anti‑invasion effects of Bruceine D in human triple‑negative breast cancer MDA‑MB‑231 cells. Experimental and Therapeutic Medicine, 19, 273-279. https://doi.org/10.3892/etm.2019.8187
MLA
Luo, C., Wang, Y., Wei, C., Chen, Y., Ji, Z."The anti‑migration and anti‑invasion effects of Bruceine D in human triple‑negative breast cancer MDA‑MB‑231 cells". Experimental and Therapeutic Medicine 19.1 (2020): 273-279.
Chicago
Luo, C., Wang, Y., Wei, C., Chen, Y., Ji, Z."The anti‑migration and anti‑invasion effects of Bruceine D in human triple‑negative breast cancer MDA‑MB‑231 cells". Experimental and Therapeutic Medicine 19, no. 1 (2020): 273-279. https://doi.org/10.3892/etm.2019.8187
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