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Osthole induces G2/M arrest and apoptosis in lung cancer A549 cells by modulating PI3K/Akt pathway
1Department of Respiratory Medicine, the Shengjing Hospital, China Medical University, Shenyang 110004, PR China.
Background:
To explore the effects of Osthole on the proliferation, cell cycle and apoptosis of human lung cancer A549 cells.
Methods:
Human lung cancer A549 cells were treated with Osthole at different concentrations. Cell proliferation was measured using the MTT assay. Cell cycle was evaluated using DNA flow cytometry analysis. Induction of apoptosis was determined by flow cytometry and fluorescent microscopy. The expressions of Cyclin B1, p-Cdc2, Bcl-2, Bax, t-Akt and p-Akt were evaluated by Western blotting.
Results:
Osthole inhibited the growth of human lung cancer A549 cells by inducing G2/M arrest and apoptosis. Western blotting demonstrated that Osthole down-regulated the expressions of Cyclin B1, p-Cdc2 and Bcl-2 and up-regulated the expressions of Bax in A549 cells. Inhibition of PI3K/Akt signaling pathway was also observed after treating A549 cells with Osthole.
Conclusions:
Our findings suggest that Osthole may have a therapeutic application in the treatment of human lung cancer.
Insights
Osthole effectively inhibits human lung cancer A549 cell growth by inducing cell cycle arrest and apoptosis. This natural compound shows promise for lung cancer treatment.
Area of Science:
- Pharmacology
- Oncology
- Molecular Biology
Background:
- Lung cancer remains a leading cause of cancer-related mortality worldwide.
- Novel therapeutic agents are urgently needed to improve treatment outcomes.
- Osthole, a natural coumarin, has demonstrated potential anti-cancer properties.
Purpose of the Study:
- To investigate the effects of Osthole on human lung cancer A549 cell proliferation, cell cycle progression, and apoptosis.
- To elucidate the molecular mechanisms underlying Osthole's anti-cancer activity.
Main Methods:
- Human lung cancer A549 cells were treated with varying concentrations of Osthole.
- Cell proliferation was assessed using the MTT assay.
- Cell cycle distribution and apoptosis were analyzed via flow cytometry and fluorescent microscopy.
- Protein expression levels (Cyclin B1, p-Cdc2, Bcl-2, Bax, t-Akt, p-Akt) were determined by Western blotting.
Main Results:
- Osthole significantly inhibited A549 cell proliferation and induced G2/M cell cycle arrest.
- Osthole promoted apoptosis in A549 cells.
- Osthole treatment led to down-regulation of Cyclin B1, p-Cdc2, Bcl-2, and up-regulation of Bax.
- Inhibition of the PI3K/Akt signaling pathway was observed.
Conclusions:
- Osthole exhibits anti-cancer effects against human lung cancer A549 cells.
- Osthole exerts its effects by modulating cell cycle regulators, apoptosis-related proteins, and the PI3K/Akt pathway.
- Osthole demonstrates potential as a therapeutic agent for human lung cancer.
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