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Wogonin suppresses the LPS‑enhanced invasiveness of MDA‑MB‑231 breast cancer cells by inhibiting the 5‑LO/BLT2 cascade

  • Authors:
    • Ji‑Hyun Go
    • Jun‑Dong Wei
    • Jae‑In Park
    • Kyung‑Seop Ahn
    • Jae‑Hong Kim
  • View Affiliations / Copyright

    Affiliations: College of Life Sciences and Biotechnology, Korea University, Seoul 02841, Republic of Korea, Natural Medicine Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), Cheongju‑si, Chungbuk 28116, Republic of Korea
    Copyright: © Go et al. This is an open access article distributed under the terms of Creative Commons Attribution License.
  • Pages: 1899-1908
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    Published online on: July 12, 2018
       https://doi.org/10.3892/ijmm.2018.3776
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Abstract

Wogonin, a naturally occurring bioactive monoflavonoid isolated from Scutellariae radix (roots of Scutellariae baicalensis Georgi), has known anticancer effects. However, the molecular signaling mechanism by which wogonin inhibits invasiveness in breast cancer cells remains unclear. In the present study, it was observed that wogonin exerted an inhibitory effect on the lipopolysaccharide (LPS)‑enhanced invasiveness of MDA‑MB‑231 cells. In addition, wogonin inhibited the synthesis of interleukin‑8 (IL‑8) and matrix metallopeptidase‑9 (MMP‑9), which are critical for promoting invasiveness in MDA‑MB‑231 cells. Wogonin also suppressed the expression of leukotriene B4 receptor 2 (BLT2) and the synthesis of its ligand, by inhibiting 5‑lipoxygenase (5‑LO) in LPS‑stimulated MDA‑MB‑231 cells. Notably, wogonin attenuated the production of IL‑8 and MMP‑9 by inhibiting the BLT2/extracellular signal‑regulated kinase (ERK)‑linked cascade. Finally, in vivo, LPS‑driven MDA‑MB‑231 cell metastasis was markedly suppressed by wogonin administration. Overall, the present results suggested that wogonin inhibited the 5‑LO/BLT2/ERK/IL‑8/MMP‑9 signaling cascade and demonstrated that this cascade may be an important target through which wogonin exerts its anticancer effects in breast cancer.
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Copy and paste a formatted citation
Spandidos Publications style
Go JH, Wei JD, Park JI, Ahn KS and Kim JH: Wogonin suppresses the LPS‑enhanced invasiveness of MDA‑MB‑231 breast cancer cells by inhibiting the 5‑LO/BLT2 cascade. Int J Mol Med 42: 1899-1908, 2018.
APA
Go, J., Wei, J., Park, J., Ahn, K., & Kim, J. (2018). Wogonin suppresses the LPS‑enhanced invasiveness of MDA‑MB‑231 breast cancer cells by inhibiting the 5‑LO/BLT2 cascade. International Journal of Molecular Medicine, 42, 1899-1908. https://doi.org/10.3892/ijmm.2018.3776
MLA
Go, J., Wei, J., Park, J., Ahn, K., Kim, J."Wogonin suppresses the LPS‑enhanced invasiveness of MDA‑MB‑231 breast cancer cells by inhibiting the 5‑LO/BLT2 cascade". International Journal of Molecular Medicine 42.4 (2018): 1899-1908.
Chicago
Go, J., Wei, J., Park, J., Ahn, K., Kim, J."Wogonin suppresses the LPS‑enhanced invasiveness of MDA‑MB‑231 breast cancer cells by inhibiting the 5‑LO/BLT2 cascade". International Journal of Molecular Medicine 42, no. 4 (2018): 1899-1908. https://doi.org/10.3892/ijmm.2018.3776
Copy and paste a formatted citation
x
Spandidos Publications style
Go JH, Wei JD, Park JI, Ahn KS and Kim JH: Wogonin suppresses the LPS‑enhanced invasiveness of MDA‑MB‑231 breast cancer cells by inhibiting the 5‑LO/BLT2 cascade. Int J Mol Med 42: 1899-1908, 2018.
APA
Go, J., Wei, J., Park, J., Ahn, K., & Kim, J. (2018). Wogonin suppresses the LPS‑enhanced invasiveness of MDA‑MB‑231 breast cancer cells by inhibiting the 5‑LO/BLT2 cascade. International Journal of Molecular Medicine, 42, 1899-1908. https://doi.org/10.3892/ijmm.2018.3776
MLA
Go, J., Wei, J., Park, J., Ahn, K., Kim, J."Wogonin suppresses the LPS‑enhanced invasiveness of MDA‑MB‑231 breast cancer cells by inhibiting the 5‑LO/BLT2 cascade". International Journal of Molecular Medicine 42.4 (2018): 1899-1908.
Chicago
Go, J., Wei, J., Park, J., Ahn, K., Kim, J."Wogonin suppresses the LPS‑enhanced invasiveness of MDA‑MB‑231 breast cancer cells by inhibiting the 5‑LO/BLT2 cascade". International Journal of Molecular Medicine 42, no. 4 (2018): 1899-1908. https://doi.org/10.3892/ijmm.2018.3776
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