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논문 기본 정보

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학술저널
저자정보
Ban, Jung-Ok (College of Pharmacy, Chungju National University) Cho, Jin-Suk (College of Pharmacy, Chungju National University) Hwang, In-Guk (College of Agriculture, Life and Environments Sciences, Chungju National University) Noh, Jin-Woo (College of Agriculture, Life and Environments Sciences, Chungju National University) Kim, Wun-Jae (Departments of Urology and Biochemistry [SCB], College of Medicine, Institute for Tumor Research, Chungju National University) Lee, Ung-Soo (Department of Food and Biotechnology, Chungju National University) Moon, Dong-Cheul (College of Pharmacy, Chungju National University) Jeong, Heon-Sang (College of Agriculture, Life and Environments Sciences, Chungju National University) Lee, Hee-Soon (College of Pharmacy, Chungju National University) Hwang, Bang-Yeon (College of Pharmacy, Chungju National University) Jung, Jae-Kyung (College of Pharmacy, Chungju National University) Han, Sang-Bae (College of Pharmacy, Chungju National University) Hong, Jin-Tae (College of Pharmacy, Chungju National University)
저널정보
한국응용약물학회 Biomolecules & Therapeutics(구 응용약물학회지) Biomolecules & therapeutics 제17권 제4호
발행연도
2009.1
수록면
403 - 411 (9page)

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Thiacremonone, the main component isolated from heated garlic (Allium sativum L.), is interested for using as a cancer preventive or therapeutic agent since garlic has been known to be useful plant in the treatment of cancers. Nuclear factor kappaB (NF-${\kappa}B$) is constitutively activated in the prostate cancer and activation of NF-${\kappa}B$ is implicated in drug resistance in cancer cells. Docetaxel, a semisynthetic analog of paclitaxel, is an antineoplastic drug widely used for advanced various cancer. In previous studies, we found that thiacremonone inhibited activation of NF-${\kappa}B$ in cancer cells and marcrophages. In the present study, we investigated whether thiacremonone could increase susceptibility of prostate cancer cells (PC-3 and DU145) to docetaxel via inactivation of NF-${\kappa}B$. We found that the combination treatment of thiacremonone (50 ${\mu}g$/ml) with docetaxel (5 nM) was more effective in the inhibition of prostate cancer cell growth and induction of apoptosis accompanied with the significant inhibition of NF-${\kappa}B$ activity than those by the treatment of thiacremonone or docetaxel alone. It was also found that NF-${\kappa}B$ target gene expression of Bax, caspase-3 and caspase-9 was much more significantly enhanced, but the expression of Bcl-2 was also much more significantly inhibited by the combination treatment. These results indicate that thiacremonone inhibits NF-${\kappa}B$, and enhances the susceptibility of prostate cancer cells to docetaxel. Thus, thiacremonone could be useful as an adjuvant anti-cancer agent.

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