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A Bioluminescent and Fluorescent Orthotopic Syngeneic Murine Model of Androgen-dependent and Castration-resistant Prostate Cancer
Published on: March 6, 2018
Androgen receptor and E2F-1 targeted thymoquinone therapy for hormone-refractory prostate cancer
Ahmed O Kaseb1, Kannagi Chinnakannu, Di Chen
1Department of Hematology/Oncology, Henry Ford Hospital, MI 458202, USA.
Abstract:
Relapse of prostate cancer after androgen ablation therapy is hormone-refractory, with continued tumor growth being dependent on the androgen receptor (AR). E2F-1, a regulator of cell proliferation and viability, reportedly plays a role in the development of hormone-refractory prostate cancer. Thymoquinone is a component of Nigella sativa, an herb used for thousands of years for culinary and medicinal purposes in Asian and Middle Eastern countries and has been reported to have an antineoplastic effect both in vitro and in vivo. We observed that thymoquinone inhibited DNA synthesis, proliferation, and viability of cancerous (LNCaP, C4-B, DU145, and PC-3) but not noncancerous (BPH-1) prostate epithelial cells by down-regulating AR and E2F-1. In LNCaP cells, this was associated with a dramatic increase in p21(Cip1), p27(Kip1), and Bax. Thymoquinone blunted progression of synchronized LNCaP cells from G1 to S phase, with a concomitant decrease in AR and E2F-1 as well as the E2F-1-regulated proteins necessary for cell cycle progression. In a xenograft prostate tumor model, thymoquinone inhibited growth of C4-2B-derived tumors in nude mice. This in vivo suppression of tumor growth, as with C4-2B cell growth in culture, was associated with a dramatic decrease in AR, E2F-1, and cyclin A as determined by Western blot of tissue extracts. Tissue immunohistochemical staining confirmed a marked reduction in E2F-1 and showed induction of apoptosis on terminal deoxyribonucleotidyl transferase-mediated dUTP nick end labeling assay. These findings show that thymoquinone suppresses the expression of AR and E2F-1 necessary for proliferation and viability of androgen-sensitive as well as androgen-independent prostate cancer cells both in vitro and in vivo and, moreover, produced no noticeable side effects in mice. We conclude that thymoquinone, a naturally occurring herbal product, may prove to be effective in treating hormone-sensitive as well as hormone-refractory prostate cancer. Furthermore, because of its selective effect on cancer cells, we believe that thymoquinone can also be used safely to help prevent the development of prostate cancer.
Insights
Thymoquinone, derived from Nigella sativa, effectively inhibits prostate cancer cell growth and tumor development by down-regulating androgen receptor (AR) and E2F-1. This natural compound shows promise for treating hormone-sensitive and hormone-refractory prostate cancer with no observed side effects.
Area of Science:
- Oncology
- Molecular Biology
- Natural Products Chemistry
Background:
- Prostate cancer relapse after androgen ablation therapy leads to hormone-refractory tumors dependent on androgen receptor (AR).
- E2F-1, a key regulator of cell proliferation and viability, is implicated in hormone-refractory prostate cancer development.
- Thymoquinone, a component of Nigella sativa, exhibits known antineoplastic effects.
Purpose of the Study:
- To investigate the efficacy of thymoquinone in inhibiting prostate cancer cell proliferation and tumor growth.
- To elucidate the molecular mechanisms underlying thymoquinone's anti-cancer effects, focusing on AR and E2F-1.
- To evaluate the safety and therapeutic potential of thymoquinone for both hormone-sensitive and hormone-refractory prostate cancer.
Main Methods:
- In vitro studies using human prostate cancer cell lines (LNCaP, C4-B, DU145, PC-3) and noncancerous cells (BPH-1).
- In vivo studies using a xenograft prostate tumor model in nude mice.
- Molecular analyses including Western blotting, immunohistochemistry, and cell cycle progression assays.
Main Results:
- Thymoquinone inhibited DNA synthesis, proliferation, and viability of prostate cancer cells by down-regulating AR and E2F-1.
- Treatment led to increased p21(Cip1), p27(Kip1), and Bax expression, and cell cycle arrest at G1 phase.
- Thymoquinone suppressed tumor growth in vivo, associated with decreased AR, E2F-1, and cyclin A, and induced apoptosis.
- No noticeable side effects were observed in mice.
Conclusions:
- Thymoquinone effectively suppresses AR and E2F-1 expression, crucial for prostate cancer cell proliferation and survival.
- The findings support thymoquinone's potential as a therapeutic agent for hormone-sensitive and hormone-refractory prostate cancer.
- Thymoquinone's selective action on cancer cells suggests its potential use in prostate cancer prevention.
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