Herb medicine Bo-du-san induces caspase dependent apoptosis and cell cycle arrest human gastric cancer cells, SNU-1

보두산(寶豆散)에 의한 SNU-1 세포의 Apoptosis 유도와 Cell cycle arrest

  • Yun, Hyun-Joung (Department of Prescriptionology, College of Oriental Medicine, Dongguk University) ;
  • Seo, Gyo-Soo (Department of Prescriptionology, College of Oriental Medicine, Dongguk University) ;
  • Choi, Jae-Woo (Department of Prescriptionology, College of Oriental Medicine, Dongguk University) ;
  • Lee, Hyun-Woo (Department of Prescriptionology, College of Oriental Medicine, Dongguk University) ;
  • Heo, Sook-Kyoung (Department of Prescriptionology, College of Oriental Medicine, Dongguk University) ;
  • Park, Won-Hwan (Department of Prescriptionology, College of Oriental Medicine, Dongguk University) ;
  • Park, Sun-Dong (Department of Prescriptionology, College of Oriental Medicine, Dongguk University)
  • 윤현정 (동국대학교 한의과대학 방제학교실) ;
  • 서교수 (동국대학교 한의과대학 방제학교실) ;
  • 최재우 (동국대학교 한의과대학 방제학교실) ;
  • 이현우 (동국대학교 한의과대학 방제학교실) ;
  • 허숙경 (동국대학교 한의과대학 방제학교실) ;
  • 박원환 (동국대학교 한의과대학 방제학교실) ;
  • 박선동 (동국대학교 한의과대학 방제학교실)
  • Published : 2007.06.30

Abstract

Objectives : The purpose of this study was to investigate the effect of Bo-du-san (BOS) on apoptosis in human gastric cancer cells, SNU-l cells. BOS, a drug preparation consisting of two herbs, that is, Crotonis Fructus (Strychni ignatii Semen, bodu in Korean) and Glycyrrhizae Radix (Glycyrrhizae uralensis FISCH, Gamcho in Korean). Methodss : In this study, methanol extract of BOS was examined for cytotoxic activity on human gastric cancer cells, SNU-1 cells, using XTT assay, with an IC50 value was 0.7 mg/ml and 0.3 mg/ml at 24 hrs and 48 hrs, respectively. Apoptosis induction by BDS in SNU-l cells was verified by the induction of DNA fragmentation, cleavage of poly ADP-ribose polymerase (PARP), and activation of caspase-3, -8 and -9. Inhibitors of caspase-3, -8 and -9 (Ac-DEVD-CHO, Z-IETD-FMK and Z-LEHD-FMK) efficiently blocked BOS-induced cell death of SNU-l. Resultss : BOS-induced cell death was via caspase dependent apoptosis. Moreover, treatment of BOS result in the decrease the G1/S cycle regulation proteins (cyclin D1 and E) expression and increase CDK inhibitor proteins (p21 and p27) expression, and increase apoptotic protein, p53 expression. Thus, BOS induces apoptosis in SNU-1 cells via cell cycle arrested in G1 phase. Conclusions : These results indicated that BOS has some potential for use as an anti-cancer agent.

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