MiR-520h-mediated FOXC2 regulation is critical for inhibition of lung cancer progression by resveratrol

Y. H. Yu, H. A. Chen, P. S. Chen, Y. J. Cheng, W. H. Hsu, Y. W. Chang, Y. H. Chen, Y. Jan, M. Hsiao, T. Y. Chang, Y. H. Liu, Y. M. Jeng, C. H. Wu, M. T. Huang, Yen-Hao Su, M. C. Hung, M. H. Chien, C. Y. Chen, M. L. Kuo, J. L. Su

Research output: Contribution to journalArticle

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Abstract

Resveratrol, a phytochemical found in various plants and Chinese herbs, is associated with multiple tumor-suppressing activities, has been tested in clinical trials. However, the molecular mechanisms involved in resveratrol-mediated tumor suppressing activities are not yet completely defined. Here, we showed that treatment with resveratrol inhibited cell mobility through induction of the mesenchymal-epithelial transition (MET) in lung cancer cells. We also found that downregulation of FOXC2 (forkhead box C2) is critical for resveratrol-mediated suppression of tumor metastasis in an in vitro and in vivo models. We also identified a signal cascade, namely, resveratrol - |miRNA-520h - |PP2A/C - |Akt → NF-κB → FOXC2, in which resveratrol inhibited the expression of FOXC2 through regulation of miRNA-520h-mediated signal cascade. This study identified a new miRNA-520h-related signal cascade involved in resveratrol-mediated tumor suppression activity and provide the clinical significances of miR-520h, PP2A/C and FOXC2 in lung cancer patients. Our results indicated a functional link between resveratrol-mediated miRNA-520h regulation and tumor suppressing ability, and provide a new insight into the role of resveratrol-induced molecular and epigenetic regulations in tumor suppression.

Original languageEnglish
Pages (from-to)431-443
Number of pages13
JournalOncogene
Volume32
Issue number4
DOIs
Publication statusPublished - Jan 24 2013

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Lung Neoplasms
MicroRNAs
Neoplasms
resveratrol
Epithelial-Mesenchymal Transition
Phytochemicals
Epigenomics
Down-Regulation
Clinical Trials
Neoplasm Metastasis

Keywords

  • FOXC2
  • metastasis
  • miR-520h
  • resveratrol

ASJC Scopus subject areas

  • Molecular Biology
  • Cancer Research
  • Genetics

Cite this

Yu, Y. H., Chen, H. A., Chen, P. S., Cheng, Y. J., Hsu, W. H., Chang, Y. W., ... Su, J. L. (2013). MiR-520h-mediated FOXC2 regulation is critical for inhibition of lung cancer progression by resveratrol. Oncogene, 32(4), 431-443. https://doi.org/10.1038/onc.2012.74

MiR-520h-mediated FOXC2 regulation is critical for inhibition of lung cancer progression by resveratrol. / Yu, Y. H.; Chen, H. A.; Chen, P. S.; Cheng, Y. J.; Hsu, W. H.; Chang, Y. W.; Chen, Y. H.; Jan, Y.; Hsiao, M.; Chang, T. Y.; Liu, Y. H.; Jeng, Y. M.; Wu, C. H.; Huang, M. T.; Su, Yen-Hao; Hung, M. C.; Chien, M. H.; Chen, C. Y.; Kuo, M. L.; Su, J. L.

In: Oncogene, Vol. 32, No. 4, 24.01.2013, p. 431-443.

Research output: Contribution to journalArticle

Yu, YH, Chen, HA, Chen, PS, Cheng, YJ, Hsu, WH, Chang, YW, Chen, YH, Jan, Y, Hsiao, M, Chang, TY, Liu, YH, Jeng, YM, Wu, CH, Huang, MT, Su, Y-H, Hung, MC, Chien, MH, Chen, CY, Kuo, ML & Su, JL 2013, 'MiR-520h-mediated FOXC2 regulation is critical for inhibition of lung cancer progression by resveratrol', Oncogene, vol. 32, no. 4, pp. 431-443. https://doi.org/10.1038/onc.2012.74
Yu, Y. H. ; Chen, H. A. ; Chen, P. S. ; Cheng, Y. J. ; Hsu, W. H. ; Chang, Y. W. ; Chen, Y. H. ; Jan, Y. ; Hsiao, M. ; Chang, T. Y. ; Liu, Y. H. ; Jeng, Y. M. ; Wu, C. H. ; Huang, M. T. ; Su, Yen-Hao ; Hung, M. C. ; Chien, M. H. ; Chen, C. Y. ; Kuo, M. L. ; Su, J. L. / MiR-520h-mediated FOXC2 regulation is critical for inhibition of lung cancer progression by resveratrol. In: Oncogene. 2013 ; Vol. 32, No. 4. pp. 431-443.
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