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Article Open Access

Resveratrol inhibits the invasion and metastasis of colon cancer through reversal of epithelial‑ mesenchymal transition via the AKT/GSK‑3β/Snail signaling pathway

Corrigendum in: /10.3892/mmr.2022.12870
  • Authors:
    • Li Yuan
    • Mengmeng Zhou
    • Dawei Huang
    • Harpreet S. Wasan
    • Kai Zhang
    • Leitao Sun
    • Hong Huang
    • Shenglin Ma
    • Minhe Shen
    • Shanming Ruan
  • View Affiliations / Copyright

    Affiliations: The First Clinical Medical College of Zhejiang Chinese Medical University, Hangzhou, Zhejiang 310053, P.R. China, Department of Traditional Chinese Medicine, The First People's Hospital of Quzhou, Quzhou, Zhejiang 324000, P.R. China, Department of Chinese Medicine, The First Affiliated Hospital of Zhejiang Chinese Medical University, Hangzhou, Zhejiang 310006, P.R. China, Department of Cancer Medicine, Hammersmith Hospital, Imperial College Healthcare NHS Trust, London W12 0HS, UK, Teaching and Research Section of Prescription, Basic Medical College, Zhejiang Chinese Medical University, Hangzhou, Zhejiang 310053, P.R. China, Department of Medical Oncology, The Fourth Affiliated Hospital of Zhejiang Chinese Medical University, Hangzhou, Zhejiang 310006, P.R. China, Department of Medical Oncology, The First Affiliated Hospital of Zhejiang Chinese Medical University, Hangzhou, Zhejiang 310006, P.R. China
    Copyright: © Yuan et al. This is an open access article distributed under the terms of Creative Commons Attribution License.
  • Pages: 2783-2795
    |
    Published online on: July 25, 2019
       https://doi.org/10.3892/mmr.2019.10528
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Abstract

The identification of safe and effective drugs that inhibit tumor invasion and metastasis is required to improve the clinical outcome of patients with colon cancer. The present study aimed to investigate the inhibitory effects and possible mechanisms of action of resveratrol against the invasion and metastasis of colon cancer. AKT1‑knockdown SW480 and SW620 colon cancer cells were used to detect the effects of resveratrol on cell invasion and metastasis, as well as changes in the expression of epithelial‑mesenchymal transition (EMT) markers and serine/threonine kinase (AKT)/glycogen synthase kinase (GSK)‑3β/Snail signaling pathway‑related molecules in vitro. Furthermore, nude mice were inoculated with SW480 cells in the tail vein to establish an in vivo lung metastasis model of colon cancer, to investigate the effects of resveratrol on lung metastasis in colon cancer. The results revealed that resveratrol treatment and AKT1 knockdown significantly inhibited cell migration and invasion in colon cancer, and markedly increased E‑cadherin expression and decreased that of N‑cadherin, phospho (p)‑AKT1, p‑GSK‑3β, and Snail in colon cancer both in vitro and in vivo. Furthermore, the effects of resveratrol were significantly weaker in the AKT1‑knockdown cells. In conclusion, resveratrol may suppress the invasion and metastasis of colon cancer through reversal of EMT via the AKT/GSK‑3β/Snail signaling pathway. AKT1 may therefore be a key regulator of EMT in colon cancer cells and a potential therapeutic target for this disease.
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Copy and paste a formatted citation
Spandidos Publications style
Yuan L, Zhou M, Huang D, Wasan HS, Zhang K, Sun L, Huang H, Ma S, Shen M, Ruan S, Ruan S, et al: Resveratrol inhibits the invasion and metastasis of colon cancer through reversal of epithelial‑ mesenchymal transition via the AKT/GSK‑3β/Snail signaling pathway Corrigendum in /10.3892/mmr.2022.12870. Mol Med Rep 20: 2783-2795, 2019.
APA
Yuan, L., Zhou, M., Huang, D., Wasan, H.S., Zhang, K., Sun, L. ... Ruan, S. (2019). Resveratrol inhibits the invasion and metastasis of colon cancer through reversal of epithelial‑ mesenchymal transition via the AKT/GSK‑3β/Snail signaling pathway Corrigendum in /10.3892/mmr.2022.12870. Molecular Medicine Reports, 20, 2783-2795. https://doi.org/10.3892/mmr.2019.10528
MLA
Yuan, L., Zhou, M., Huang, D., Wasan, H. S., Zhang, K., Sun, L., Huang, H., Ma, S., Shen, M., Ruan, S."Resveratrol inhibits the invasion and metastasis of colon cancer through reversal of epithelial‑ mesenchymal transition via the AKT/GSK‑3β/Snail signaling pathway Corrigendum in /10.3892/mmr.2022.12870". Molecular Medicine Reports 20.3 (2019): 2783-2795.
Chicago
Yuan, L., Zhou, M., Huang, D., Wasan, H. S., Zhang, K., Sun, L., Huang, H., Ma, S., Shen, M., Ruan, S."Resveratrol inhibits the invasion and metastasis of colon cancer through reversal of epithelial‑ mesenchymal transition via the AKT/GSK‑3β/Snail signaling pathway Corrigendum in /10.3892/mmr.2022.12870". Molecular Medicine Reports 20, no. 3 (2019): 2783-2795. https://doi.org/10.3892/mmr.2019.10528
Copy and paste a formatted citation
x
Spandidos Publications style
Yuan L, Zhou M, Huang D, Wasan HS, Zhang K, Sun L, Huang H, Ma S, Shen M, Ruan S, Ruan S, et al: Resveratrol inhibits the invasion and metastasis of colon cancer through reversal of epithelial‑ mesenchymal transition via the AKT/GSK‑3β/Snail signaling pathway Corrigendum in /10.3892/mmr.2022.12870. Mol Med Rep 20: 2783-2795, 2019.
APA
Yuan, L., Zhou, M., Huang, D., Wasan, H.S., Zhang, K., Sun, L. ... Ruan, S. (2019). Resveratrol inhibits the invasion and metastasis of colon cancer through reversal of epithelial‑ mesenchymal transition via the AKT/GSK‑3β/Snail signaling pathway Corrigendum in /10.3892/mmr.2022.12870. Molecular Medicine Reports, 20, 2783-2795. https://doi.org/10.3892/mmr.2019.10528
MLA
Yuan, L., Zhou, M., Huang, D., Wasan, H. S., Zhang, K., Sun, L., Huang, H., Ma, S., Shen, M., Ruan, S."Resveratrol inhibits the invasion and metastasis of colon cancer through reversal of epithelial‑ mesenchymal transition via the AKT/GSK‑3β/Snail signaling pathway Corrigendum in /10.3892/mmr.2022.12870". Molecular Medicine Reports 20.3 (2019): 2783-2795.
Chicago
Yuan, L., Zhou, M., Huang, D., Wasan, H. S., Zhang, K., Sun, L., Huang, H., Ma, S., Shen, M., Ruan, S."Resveratrol inhibits the invasion and metastasis of colon cancer through reversal of epithelial‑ mesenchymal transition via the AKT/GSK‑3β/Snail signaling pathway Corrigendum in /10.3892/mmr.2022.12870". Molecular Medicine Reports 20, no. 3 (2019): 2783-2795. https://doi.org/10.3892/mmr.2019.10528
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