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Total triterpenoids from Ganoderma Lucidum suppresses prostate cancer cell growth by inducing growth arrest and
Tao Wang1,2, Zi-Ping Xie3, Zhan-Sen Huang4
1Department of Urology, Medical Center for Overseas Patients, Nanfang Hospital, Southern Medical University, Guangzhou, 510515, China.
Abstract:
In this study, one immortalized human normal prostatic epithelial cell line (BPH) and four human prostate cancer cell lines (LNCaP, 22Rv1, PC-3, and DU-145) were treated with Ganoderma Lucidum triterpenoids (GLT) at different doses and for different time periods. Cell viability, apoptosis, and cell cycle were analyzed using flow cytometry and chemical assays. Gene expression and binding to DNA were assessed using real-time PCR and Western blotting. It was found that GLT dose-dependently inhibited prostate cancer cell growth through induction of apoptosis and cell cycle arrest at G1 phase. GLT-induced apoptosis was due to activation of Caspases-9 and -3 and turning on the downstream apoptotic events. GLT-induced cell cycle arrest (mainly G1 arrest) was due to up-regulation of p21 expression at the early time and down-regulation of cyclin-dependent kinase 4 (CDK4) and E2F1 expression at the late time. These findings demonstrate that GLT suppresses prostate cancer cell growth by inducing growth arrest and apoptosis, which might suggest that GLT or Ganoderma Lucidum could be used as a potential therapeutic drug for prostate cancer.
Insights
Ganoderma Lucidum triterpenoids (GLT) inhibit prostate cancer cell growth by inducing apoptosis and cell cycle arrest. These findings suggest Ganoderma Lucidum as a potential therapeutic for prostate cancer.
Area of Science:
- Oncology
- Pharmacology
- Molecular Biology
Background:
- Prostate cancer remains a leading cause of cancer-related deaths globally.
- Novel therapeutic strategies are crucial for effective prostate cancer treatment.
- Ganoderma lucidum has traditional medicinal uses, but its specific anti-cancer mechanisms require elucidation.
Purpose of the Study:
- To investigate the anti-cancer effects of Ganoderma lucidum triterpenoids (GLT) on human prostate cancer cell lines.
- To elucidate the molecular mechanisms underlying GLT-induced inhibition of prostate cancer cell growth.
- To assess the potential of GLT as a therapeutic agent for prostate cancer.
Main Methods:
- Utilized human prostate cancer cell lines (LNCaP, 22Rv1, PC-3, DU-145) and a normal prostatic epithelial cell line (BPH).
- Treated cells with varying doses and durations of GLT.
- Analyzed cell viability, apoptosis, and cell cycle via flow cytometry and chemical assays.
- Assessed gene expression and DNA binding using real-time PCR and Western blotting.
Main Results:
- GLT demonstrated dose-dependent inhibition of prostate cancer cell growth.
- GLT induced apoptosis through activation of Caspase-9 and Caspase-3.
- GLT caused cell cycle arrest at the G1 phase, involving p21 up-regulation and CDK4/E2F1 down-regulation.
Conclusions:
- GLT effectively suppresses prostate cancer cell proliferation by inducing apoptosis and cell cycle arrest.
- The molecular pathways involve caspase activation and modulation of cell cycle regulatory proteins.
- Ganoderma lucidum triterpenoids show promise as a potential therapeutic for prostate cancer.
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