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Article Open Access

Resveratrol suppresses melanoma growth by promoting autophagy through inhibiting the PI3K/AKT/mTOR signaling pathway

Retraction in: /10.3892/etm.2024.12668
  • Authors:
    • Changhua Gong
    • Honglei Xia
  • View Affiliations / Copyright

    Affiliations: Department of Pharmacy, People's Hospital of Zhenhai, Ningbo, Zhejiang 315202, P.R. China
    Copyright: © Gong et al. This is an open access article distributed under the terms of Creative Commons Attribution License.
  • Pages: 1878-1886
    |
    Published online on: December 20, 2019
       https://doi.org/10.3892/etm.2019.8359
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Abstract

Resveratrol (RV) is a natural polyphenolic phytoalexin derived from peanuts, red grape skins and red wine, and has been demonstrated to alleviate multiple types of malignancies. However, how RV achieves this in melanoma is unknown. The aim of present study was to investigate the role of RV in melanoma, using Cell Counting Kit‑8, flow cytometry and western blot analysis. RV inhibited melanoma cell viability, migration and invasion counteracting melanoma progression. In addition, proteins associated with autophagy, including Beclin 1 and microtubule‑associated protein 1A/1B‑light chain 3 (LC3)‑II/I, were upregulated, whereas p62 expression was downregulated in RV‑treated cells. The number of LC3+ puncta, which can be applied to represent autophagosome formation, increased following RV treatment, suggesting that RV may trigger autophagy in melanoma cells. Treatment with the autophagy inhibitor, 3‑methyladenine, reversed the RV‑dependent inhibition of viability, migration and invasion of melanoma cells. RV treatment also reduced the ratios of phosphorylated (p)‑AKT/AKT and p‑mTOR/mTOR in melanoma cells. In conclusion, these findings suggested that RV may inhibit the viability and migration of melanoma cells through inhibiting the AKT/mTOR pathway, thus triggering autophagy. This indicated that RV may serve as an innovative therapeutic for melanoma treatment.
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Copy and paste a formatted citation
Spandidos Publications style
Gong C and Xia H: Resveratrol suppresses melanoma growth by promoting autophagy through inhibiting the PI3K/AKT/mTOR signaling pathway Retraction in /10.3892/etm.2024.12668. Exp Ther Med 19: 1878-1886, 2020.
APA
Gong, C., & Xia, H. (2020). Resveratrol suppresses melanoma growth by promoting autophagy through inhibiting the PI3K/AKT/mTOR signaling pathway Retraction in /10.3892/etm.2024.12668. Experimental and Therapeutic Medicine, 19, 1878-1886. https://doi.org/10.3892/etm.2019.8359
MLA
Gong, C., Xia, H."Resveratrol suppresses melanoma growth by promoting autophagy through inhibiting the PI3K/AKT/mTOR signaling pathway Retraction in /10.3892/etm.2024.12668". Experimental and Therapeutic Medicine 19.3 (2020): 1878-1886.
Chicago
Gong, C., Xia, H."Resveratrol suppresses melanoma growth by promoting autophagy through inhibiting the PI3K/AKT/mTOR signaling pathway Retraction in /10.3892/etm.2024.12668". Experimental and Therapeutic Medicine 19, no. 3 (2020): 1878-1886. https://doi.org/10.3892/etm.2019.8359
Copy and paste a formatted citation
x
Spandidos Publications style
Gong C and Xia H: Resveratrol suppresses melanoma growth by promoting autophagy through inhibiting the PI3K/AKT/mTOR signaling pathway Retraction in /10.3892/etm.2024.12668. Exp Ther Med 19: 1878-1886, 2020.
APA
Gong, C., & Xia, H. (2020). Resveratrol suppresses melanoma growth by promoting autophagy through inhibiting the PI3K/AKT/mTOR signaling pathway Retraction in /10.3892/etm.2024.12668. Experimental and Therapeutic Medicine, 19, 1878-1886. https://doi.org/10.3892/etm.2019.8359
MLA
Gong, C., Xia, H."Resveratrol suppresses melanoma growth by promoting autophagy through inhibiting the PI3K/AKT/mTOR signaling pathway Retraction in /10.3892/etm.2024.12668". Experimental and Therapeutic Medicine 19.3 (2020): 1878-1886.
Chicago
Gong, C., Xia, H."Resveratrol suppresses melanoma growth by promoting autophagy through inhibiting the PI3K/AKT/mTOR signaling pathway Retraction in /10.3892/etm.2024.12668". Experimental and Therapeutic Medicine 19, no. 3 (2020): 1878-1886. https://doi.org/10.3892/etm.2019.8359
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