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Article

Suppression of cancer stem-like phenotypes in NCI-H460 lung cancer cells by vanillin through an Akt-dependent pathway

  • Authors:
    • Songpol Srinual
    • Pithi Chanvorachote
    • Varisa Pongrakhananon
  • View Affiliations / Copyright

    Affiliations: Department of Pharmacology and Physiology, Faculty of Pharmaceutical Sciences, Chulalongkorn University, Bangkok 10330, Thailand
  • Pages: 1341-1351
    |
    Published online on: February 17, 2017
       https://doi.org/10.3892/ijo.2017.3879
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Abstract

Cancer stem cells (CSCs) have been reported as a major cause of cancer metastasis and the failure of cancer treatment. Cumulative studies have indicated that protein kinase B (Akt) and its downstream signaling pathway, including CSC markers, play a critical role in the aggressive behavior of this cancer. In this study, we investigated whether vanillin, a major component in Vanilla planifolia seed, could suppress cancer stemness phenotypes and related proteins in the human non-small cell lung cancer NCI‑H460 cell line. A non-toxic concentration of vanillin suppressed spheroid and colony formation, two hallmarks of the cancer stemness phenotype, in vitro in NCI‑H460 cells. Western blot analysis revealed that the CSC markers CD133 and ALDH1A1 and the associated transcription factors, Oct4 and Nanog, were extensively downregulated by vanillin. Vanillin also attenuated the expression and activity of Akt, a transcription regulator upstream of CSCs, an action that was confirmed by treatment with the Akt inhibitor perifosine. Furthermore, the ubiquitination of Akt was elevated in response to vanillin treatment prior to proteasomal degradation. This finding indicates that vanillin can inhibit cancer stem cell-like behavior in NCI‑H460 cells through the induction of Akt-proteasomal degradation and reduction of downstream CSC transcription factors. This inhibitory effect of vanillin may be an alternative approach in the treatment against lung cancer metastasis and its resistance to chemotherapy.
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Spandidos Publications style
Srinual S, Chanvorachote P and Pongrakhananon V: Suppression of cancer stem-like phenotypes in NCI-H460 lung cancer cells by vanillin through an Akt-dependent pathway. Int J Oncol 50: 1341-1351, 2017.
APA
Srinual, S., Chanvorachote, P., & Pongrakhananon, V. (2017). Suppression of cancer stem-like phenotypes in NCI-H460 lung cancer cells by vanillin through an Akt-dependent pathway. International Journal of Oncology, 50, 1341-1351. https://doi.org/10.3892/ijo.2017.3879
MLA
Srinual, S., Chanvorachote, P., Pongrakhananon, V."Suppression of cancer stem-like phenotypes in NCI-H460 lung cancer cells by vanillin through an Akt-dependent pathway". International Journal of Oncology 50.4 (2017): 1341-1351.
Chicago
Srinual, S., Chanvorachote, P., Pongrakhananon, V."Suppression of cancer stem-like phenotypes in NCI-H460 lung cancer cells by vanillin through an Akt-dependent pathway". International Journal of Oncology 50, no. 4 (2017): 1341-1351. https://doi.org/10.3892/ijo.2017.3879
Copy and paste a formatted citation
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Spandidos Publications style
Srinual S, Chanvorachote P and Pongrakhananon V: Suppression of cancer stem-like phenotypes in NCI-H460 lung cancer cells by vanillin through an Akt-dependent pathway. Int J Oncol 50: 1341-1351, 2017.
APA
Srinual, S., Chanvorachote, P., & Pongrakhananon, V. (2017). Suppression of cancer stem-like phenotypes in NCI-H460 lung cancer cells by vanillin through an Akt-dependent pathway. International Journal of Oncology, 50, 1341-1351. https://doi.org/10.3892/ijo.2017.3879
MLA
Srinual, S., Chanvorachote, P., Pongrakhananon, V."Suppression of cancer stem-like phenotypes in NCI-H460 lung cancer cells by vanillin through an Akt-dependent pathway". International Journal of Oncology 50.4 (2017): 1341-1351.
Chicago
Srinual, S., Chanvorachote, P., Pongrakhananon, V."Suppression of cancer stem-like phenotypes in NCI-H460 lung cancer cells by vanillin through an Akt-dependent pathway". International Journal of Oncology 50, no. 4 (2017): 1341-1351. https://doi.org/10.3892/ijo.2017.3879
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