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Geraniol inhibits prostate cancer growth by targeting cell cycle and apoptosis pathways
Su-Hwa Kim1, Hyun Cheol Bae, Eun-Jung Park
1Department of Physiology, Seoul National University College of Medicine, Seoul 110-799, Republic of Korea.
Abstract:
The progression of prostate cancer is associated with escape from cell cycle arrest and apoptosis under androgen-depleted conditions. Here, we found that geraniol, a naturally occurring monoterpene, induces cell cycle arrest and apoptosis in cultured cells and tumor grafted mice using PC-3 prostate cancer cells. Geraniol modulated the expression of various cell cycle regulators and Bcl-2 family proteins in PC-3 cells in vitro and in vivo. Furthermore, we showed that the combination of sub-optimal doses of geraniol and docetaxel noticeably suppresses prostate cancer growth in cultured cells and tumor xenograft mice. Therefore, our findings provide insight into unraveling the mechanisms underlying escape from cell cycle arrest and apoptosis and developing therapeutic strategies against prostate cancer.
Insights
Geraniol, a natural compound, halts prostate cancer progression by inducing cell death and cell cycle arrest. Combining geraniol with docetaxel enhances its therapeutic effect against prostate cancer.
Area of Science:
- Oncology
- Molecular Biology
- Natural Products Chemistry
Background:
- Prostate cancer progression involves evading cell cycle arrest and apoptosis, particularly under androgen-depleted conditions.
- Understanding the molecular mechanisms of this evasion is crucial for developing effective treatments.
Purpose of the Study:
- To investigate the effects of geraniol, a naturally occurring monoterpene, on prostate cancer cell cycle regulation and apoptosis.
- To evaluate the potential of geraniol, alone and in combination with docetaxel, as a therapeutic strategy for prostate cancer.
Main Methods:
- In vitro studies using PC-3 prostate cancer cells to assess cell cycle arrest and apoptosis.
- In vivo studies using tumor grafted mice to evaluate geraniol's efficacy and mechanism of action.
- Analysis of cell cycle regulators and Bcl-2 family protein expression.
Main Results:
- Geraniol induced significant cell cycle arrest and apoptosis in PC-3 cells, both in vitro and in vivo.
- Geraniol modulated the expression of key cell cycle regulators and Bcl-2 family proteins.
- Combination therapy with sub-optimal doses of geraniol and docetaxel markedly suppressed prostate cancer growth in cell cultures and tumor xenografts.
Conclusions:
- Geraniol demonstrates potential as an anti-cancer agent by overcoming resistance to cell cycle arrest and apoptosis in prostate cancer.
- Combined geraniol and docetaxel therapy offers a promising strategy for more effective prostate cancer treatment.
- These findings provide insights into the mechanisms of prostate cancer progression and suggest novel therapeutic avenues.
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