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Published on: March 29, 2024
Ellagic acid inhibits cell proliferation, migration, and invasion in melanoma via EGFR pathway
Fan Wang1, Jiangyan Chen1, Debing Xiang1
1Department of Oncology, Jiangjin District Central Hospital Chongqing 402260, China.
Abstract:
Ellagic acid (EA), a polyphenolic compound from pomegranate fruit extracts, has been reported to possess anti-proliferation, pro-apoptosis, and anti-invasion effects on many cancers. However, its effect on melanoma is yet to be clarified. In the present study, we investigated the anti-cancer effects of EA on melanoma cells in vitro and in vivo. The results indicated that 40 µM of EA significantly inhibited the proliferation, migration, and invasion of WM115 and A375 cells. The EA treatment significantly decreased the expression of p-EGFR and Vimentin, but increased the expression of E-cadherin in both cell lines. We further found that EGFR activation significantly abolished the effect of EA on WM115 and A375 cells. Moreover, EA treatment impaired in vivo tumorigenesis of A375 cells. Moreover, elevated pEGFR expression was an independent detrimental factor for melanoma patients. Taken together, our study provided evidence that EA treatment inhibits the migration, invasion and proliferation of melanoma cells via EGFR signaling pathway. These findings strongly suggested that EA might be useful for the development of new therapeutic strategies at melanoma.
Insights
Ellagic acid (EA) effectively inhibits melanoma cell growth, migration, and invasion by targeting the EGFR signaling pathway. This natural compound shows promise as a potential therapeutic agent for melanoma treatment.
Area of Science:
- Oncology
- Pharmacology
- Natural Products
Background:
- Melanoma is an aggressive skin cancer with limited treatment options.
- Ellagic acid (EA), a polyphenol from pomegranates, shows anti-cancer properties but its role in melanoma is unclear.
Purpose of the Study:
- To investigate the anti-cancer effects of ellagic acid (EA) on melanoma cells.
- To elucidate the mechanism of EA's action, particularly its effect on the EGFR signaling pathway.
Main Methods:
- In vitro studies using WM115 and A375 melanoma cell lines.
- In vivo experiments assessing tumor growth in mouse models.
- Analysis of key protein expressions including p-EGFR, Vimentin, and E-cadherin.
Main Results:
- EA significantly inhibited melanoma cell proliferation, migration, and invasion.
- EA decreased p-EGFR and Vimentin expression while increasing E-cadherin.
- EGFR activation diminished EA's anti-cancer effects.
- EA impaired melanoma tumor growth in vivo.
- Elevated pEGFR expression correlated with poor prognosis in melanoma patients.
Conclusions:
- Ellagic acid exerts anti-cancer effects on melanoma cells by inhibiting proliferation, migration, and invasion.
- The EGFR signaling pathway is a key mediator of EA's therapeutic effects in melanoma.
- EA demonstrates potential as a novel therapeutic strategy for melanoma treatment.
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