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Piperine Induces Apoptosis and Autophagy in HSC-3 Human Oral Cancer Cells by Regulating PI3K Signaling Pathway
Eun-Ji Han1, Eun-Young Choi1, Su-Ji Jeon1
1Laboratory Animal Science, Department of Companion, Kongju National University, Yesan-gun 32439, Republic of Korea.
Abstract:
Currently, therapies for treating oral cancer have various side effects; therefore, research on treatment methods employing natural substances is being conducted. This study aimed to investigate piperine-induced apoptosis and autophagy in HSC-3 human oral cancer cells and their effects on tumor growth in vivo. A 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay demonstrated that piperine reduced the viability of HSC-3 cells and 4',6-diamidino-2-phenylindole staining, annexin-V/propidium iodide staining, and analysis of apoptosis-related protein expression confirmed that piperine induces apoptosis in HSC-3 cells. Additionally, piperine-induced autophagy was confirmed by the observation of increased acidic vesicular organelles and autophagy marker proteins, demonstrating that autophagy in HSC-3 cells induces apoptosis. Mechanistically, piperine induced apoptosis and autophagy by inhibiting the phosphatidylinositol-3-kinase (PI3K)/protein kinase B/mammalian target of rapamycin pathway in HSC-3 cells. We also confirmed that piperine inhibits oral cancer tumor growth in vivo via antitumor effects related to apoptosis and PI3K signaling pathway inhibition. Therefore, we suggest that piperine can be considered a natural anticancer agent for human oral cancer.
Insights
Piperine, a natural compound, effectively triggers apoptosis and autophagy in human oral cancer cells, inhibiting tumor growth. This suggests piperine
Area of Science:
- Natural Product Chemistry
- Oncology
- Molecular Biology
Background:
- Current oral cancer therapies present significant side effects.
- Natural substances offer a promising avenue for developing novel cancer treatments.
- Investigating natural compounds for targeted cancer therapy is crucial.
Purpose of the Study:
- To investigate the effects of piperine on apoptosis and autophagy in human oral cancer cells (HSC-3).
- To evaluate the impact of piperine on oral cancer tumor growth in vivo.
- To elucidate the molecular mechanisms underlying piperine's anticancer effects.
Main Methods:
- Cell viability assays (MTT assay) were performed on HSC-3 cells.
- Apoptosis was assessed using DAPI staining, Annexin-V/PI staining, and Western blot analysis of apoptosis-related proteins.
- Autophagy was confirmed by observing acidic vesicular organelles and autophagy marker proteins.
- The PI3K/Akt/mTOR signaling pathway was investigated.
- In vivo tumor growth inhibition was evaluated.
Main Results:
- Piperine significantly reduced the viability of HSC-3 oral cancer cells.
- Piperine demonstrably induced apoptosis and autophagy in HSC-3 cells.
- Piperine inhibited the PI3K/Akt/mTOR signaling pathway.
- Piperine suppressed oral cancer tumor growth in vivo through apoptosis and PI3K pathway inhibition.
Conclusions:
- Piperine effectively induces apoptosis and autophagy in human oral cancer cells.
- Piperine exhibits antitumor effects in vivo by inhibiting tumor growth via apoptosis and PI3K signaling.
- Piperine holds potential as a natural anticancer agent for oral cancer treatment.
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