The Journal of Korean Medicine (대한한의학회지)
- Volume 25 Issue 3
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- Pages.191-202
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- 2004
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- 1010-0695(pISSN)
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- 2288-3339(eISSN)
Antitumor Effect of Gagamjengac-tang and $As_2O_3$ in Human Lung Cancer Cell Line, H-157
폐암세포주 H-157에서 가감증액탕과 $As_2O_3$ 의 병용처리에 의한 항종양효과
- Lee Byoung-Ho (Department of Internal Medicine, College of Oriental Medicine, Wonkwang University) ;
- Won Jin-Hee (Department of Internal Medicine, College of Oriental Medicine, Wonkwang University) ;
- Kim Dong-Woung (Department of Internal Medicine, College of Oriental Medicine, Wonkwang University) ;
- Lee Jong-Duk (Department of Internal Medicine, College of Oriental Medicine, Wonkwang University) ;
- Moon Goo (Department of Internal Medicine, College of Oriental Medicine, Wonkwang University)
- 이병호 (원광대학교 한의과대학 비계내과학 교실) ;
- 원진희 (원광대학교 한의과대학 비계내과학 교실) ;
- 김동웅 (원광대학교 한의과대학 비계내과학 교실) ;
- 이종덕 (원광대학교 한의과대학 비계내과학 교실) ;
- 문구 (원광대학교 한의과대학 비계내과학 교실)
- Published : 2004.09.01
Abstract
Objectives : This study was designed to elucidate the synergistic cytotoxic mechanisms of the co-treatment of Gagamjengac-tang (GGJAT) and As₂O₃ in human lung cancer cell line, H-157. Methods : The combination of GGJAT and As₂O₃ synergistically augmented the cytotoxicity of GGJAT and As₂O₃ in H157 cells. The cytotoxicity by the combination of these two drugs was revealed as apoptosis which was characterized by chromatin condensation and fragmentation in DAPI staining. Results : Antioxidant NAC completely blocked the apoptotic death of H-157 cells by GGJAT and As₂O₃. The apoptotic cytotoxicity of GGJAT and As₂O₃ was accompanied by the induction of DR4 and DR5 in RT-PCR. In addition, antioxidant enzymes such as SOD1, GSH synthetase and GSH reductase were also increased in H-157 cells treated with GGJAT and As₂O₃. However, of note, p53, Fas, FasL and TRAIL were not detected in H-157 cells treated with GGJAT and As₂O₃ by RT-PCR. Conclusions : These results suggest that the synergistic cytotoxicity of the co-treatment of H-457 cells treated with GGJAT and As₂O₃ may cause induction of death receptors DR4 and DR5 as well as reactive oxygen species.