전립선 암세포주 DU145의 세포고사 유도를 통한 신선초 (Angelica keiskei) 메틸렌 클로라이드 추출물의 항암효과

Antitumor Activity of Methylene Chloride Fraction from Angelica Keiskei Through Induction of Apoptosis in Human Prostate Carcinoma DU145 Cells

  • 강윤묵 (경희대학교 한의과대학 기초한의학과 병리학교실) ;
  • 김성무 (경희대학교 한의과대학 기초한의학과 병리학교실) ;
  • 김현중 (경희대학교 한의과대학 기초한의학과 병리학교실) ;
  • 박경란 (경희대학교 한의과대학 기초한의학과 병리학교실) ;
  • 심범상 (경희대학교 한의과대학 기초한의학과 병리학교실) ;
  • 김성훈 (경희대학교 한의과대학 기초한의학과 병리학교실) ;
  • 최승훈 (경희대학교 한의과대학 기초한의학과 병리학교실) ;
  • 안규석 (경희대학교 한의과대학 기초한의학과 병리학교실) ;
  • 안광석 (경희대학교 한의과대학 기초한의학과 병리학교실)
  • Kang, Yoon-Mook (Department of Oriental Pathology, College of Oriental Medicine, Kyung Hee University) ;
  • Kim, Sung-Moo (Department of Oriental Pathology, College of Oriental Medicine, Kyung Hee University) ;
  • Kim, Hyun-Jung (Department of Oriental Pathology, College of Oriental Medicine, Kyung Hee University) ;
  • Park, Kyung-Ran (Department of Oriental Pathology, College of Oriental Medicine, Kyung Hee University) ;
  • Shim, Bum-Sang (Department of Oriental Pathology, College of Oriental Medicine, Kyung Hee University) ;
  • Kim, Sung-Hoon (Department of Oriental Pathology, College of Oriental Medicine, Kyung Hee University) ;
  • Choi, Seung-Hoon (Department of Oriental Pathology, College of Oriental Medicine, Kyung Hee University) ;
  • Ahn, Kyoo-Seok (Department of Oriental Pathology, College of Oriental Medicine, Kyung Hee University) ;
  • Ahn, Kwang-Seok (Department of Oriental Pathology, College of Oriental Medicine, Kyung Hee University)
  • 투고 : 2010.12.07
  • 심사 : 2010.12.23
  • 발행 : 2010.12.28

초록

The roots and leaves of Angelica keiskei (AK) have been used for the treatment of various diseases including coronary heartdisease, hypertension, and cancer in the Korean folk medicine. However, the mechanism by which methylenechloride fraction (MF) from AK exerts anti-tumorigenic activity in human prostate cancer cells has not been fully understood. In the present study, we report the MF exerted the highest cytotoxicity against prostate cancer DU145 cells compared with other fractions. Especially, MF caused the accumulation of sub-G1 DNA contents of cell cycle and increased annexin V-positive apoptotic bodies and DNA fragmentation. MF down-regulated several proliferative (Cyclin D1) and anti-apoptotic (Bcl-xl, Bcl-2, IAP-1/2, and survivin)gene products in these cells. Hence, MF induced apoptosis through the caspase-3 activation in DU145 cells. We further confirmed that caspase-3 plays an importance role in MF-induced apoptosis in DU145 cells by using caspase-3 inhibitor. Additionally, we observed that MF potentiated Dox-induced apoptosis in DU145 cells. Taken together, our data demonstrate the evidence that MF induces apoptosis depend on caspase-3 activation of and overcomes resistance to chemotherapy in human prostate cancer cells.

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