Torilis japonica extract, a new potential EMT suppressor agent by regulation of EGFR signaling pathways

  • Authors:
    • Guen Tae Kim
    • Se Hee Lee
    • Young Min Kim
  • View Affiliations

  • Published online on: July 17, 2014     https://doi.org/10.3892/ijo.2014.2546
  • Pages: 1673-1679
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Abstract

Abnormal metastasis of carcinoma is associated with the loss of epithelial features and the acquisition of a mesenchymal phenotype. The stimulation of cells with epidermal growth factor (EGF) resulted in morphological changes and induced epithelial-mesenchymal transition (EMT). EGF stimulation resulted in increased mobility along with upregulated actin polarization related proteins, E-cadherin regulators and the mesenchymal markers. Treatment with Torilis japonica extract (TJE) along with stimulation by EGF prevented changes in cell morphology, mobility, expression of actin polarization proteins and EMT markers. Using specific inhibitors and siEGFR, it was demonstrated that TJE suppressed EMT through EGFR inactivation and regulation of its downstream signaling pathways. We suggest that TJE is a new potential reagent for EGFR-targeted therapy and anti-abnormal metastasis in MCF-7 breast cancer.
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October 2014
Volume 45 Issue 4

Print ISSN: 1019-6439
Online ISSN:1791-2423

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Spandidos Publications style
Kim GT, Lee SH and Kim YM: Torilis japonica extract, a new potential EMT suppressor agent by regulation of EGFR signaling pathways. Int J Oncol 45: 1673-1679, 2014
APA
Kim, G.T., Lee, S.H., & Kim, Y.M. (2014). Torilis japonica extract, a new potential EMT suppressor agent by regulation of EGFR signaling pathways. International Journal of Oncology, 45, 1673-1679. https://doi.org/10.3892/ijo.2014.2546
MLA
Kim, G. T., Lee, S. H., Kim, Y. M."Torilis japonica extract, a new potential EMT suppressor agent by regulation of EGFR signaling pathways". International Journal of Oncology 45.4 (2014): 1673-1679.
Chicago
Kim, G. T., Lee, S. H., Kim, Y. M."Torilis japonica extract, a new potential EMT suppressor agent by regulation of EGFR signaling pathways". International Journal of Oncology 45, no. 4 (2014): 1673-1679. https://doi.org/10.3892/ijo.2014.2546