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논문 기본 정보

자료유형
학술저널
저자정보
Choi, Kyung Eun (College of Pharmacy and Medical Research Center, Chungbuk National University) Jung, Young Suk (College of Pharmacy and Medical Research Center, Chungbuk National University) Kim, Dea Hwan (College of Pharmacy and Medical Research Center, Chungbuk National University) Song, Ju Kyung (College of Pharmacy and Medical Research Center, Chungbuk National University) Kim, Ji Young (College of Pharmacy and Medical Research Center, Chungbuk National University) Jung, Yu Yeon (College of Pharmacy and Medical Research Center, Chungbuk National University) Eum, So Young (College of Pharmacy and Medical Research Center, Chungbuk National University) Kim, Joo Hwan (Osong Health Technology Administration Complex) Yoon, Na Young (Osong Health Technology Administration Complex) Yoo, Hwan Soo (College of Pharmacy and Medical Research Center, Chungbuk National University) Han, Sang-Bae (College of Pharmacy and Medical Research Center, Chungbuk National University) Hong, Jin Tae (College of Pharmacy and Medical Research Center, Chungbuk National University)
저널정보
대한약학회 Archives of pharmacal research : a publication of the Pharmaceutical Society of Korea Archives of pharmacal research : a publication of the Pharmaceutical Society of Korea 제37권 제4호
발행연도
2014.1
수록면
501 - 511 (11page)

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It has been known that myriocin inhibits melanoma growth. However, the effects and action mechanisms of myriocin on lung cancer cell growth have not been reported. In this study, we examined whether myriocin isolated from Mycelia sterilia inhibits cell growth of lung cancer cells (A549 and NCI-H460) as well as possible signaling pathways involved in cell growth inhibition. Different concentrations of myriocin inhibited the growth of lung cancer cells through the induction of apoptotic cell death. Consistent with cancer cell growth inhibition, myriocin induced the expression of death receptors (DRs) as well as p-JNK and p-p38 in both cell lines. Moreover, the combination of myriocin with DR4 ligand TRAIL, and other well known anti-tumor drugs (docetaxel and cisplatin) synergistically inhibited cancer cell growth, and induced DR4 expression. These results showed that myriocin inhibits lung cancer cells growth through apoptosis via the activation of DR4 pathways, and enhanced anticancer effects with well known drugs. Thus, our study indicates that myriocin could be effective for lung cancer cells as an anti-cancer drug and/or a conjunction agent with well known anti-cancers.

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