Planta Med 2002; 68(2): 123-127
DOI: 10.1055/s-2002-20242
Original Paper
Pharmacology
© Georg Thieme Verlag Stuttgart · New York

Induction of Apoptosis by 3,4′-Dimethoxy-5-hydroxystilbene in Human Promyeloid Leukemic HL-60 Cells

Sung Hee Lee1 , Shi Yong Ryu2 , Han Bok Kim3 , Mie Young Kim1 , Young Jin Chun1
  • 1College of Pharmacy, Chungang University, Seoul, Korea
  • 2Korea Research Institute of Chemical Technology (KRICT), Taejon, Korea
  • 3Department of Life Science, Hoseo University, Asan, Chungcheongnam-Do, Korea
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Publikationsverlauf

February 15, 2001

May 6, 2001

Publikationsdatum:
22. Februar 2002 (online)

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Abstract

3, 4′-Dimethoxy-5-hydroxystilbene (DMHS) is a hydroxystilbene compound obtained by methylation and acid hydrolysis of piceid (resveratrol-3-O-glucoside) from Polygonum cuspidatum. Herein, we report that DMHS induces programmed cell death or apoptosis in human promyelocytic leukemic HL-60 cells. We found that treatment of HL-60 cells with DMHS suppressed the cell growth in a concentration-dependent manner with an IC50 value of 25 μM. DMHS increased internucleosomal DNA fragmentation in a time-dependent manner. The cell death by DMHS was partially prevented by the caspase inhibitor, zVAD-fmk. DMHS caused activation of caspases such as caspase-3, -8, and -9. Immunoblot experiments revealed that DMHS-induced apoptosis was associated with the induction of Bax expression. The release of cytochrome c from mitochondria into the cytosol was increased in response to DMHS. Taken together, our present results indicated that DMHS leads to apoptotic cell death in HL-60 cells through increased Bax expression and release of cytochrome c into cytosol and may be considered as a good candidate for a cancer chemopreventive agent in humans.

References

Prof. Dr. Young Jin Chun

College of Pharmacy

Chungang University

221 Huksuk-dong

Dongjak-gu

Seoul 156-756

Korea

eMail: yjchun@chungang.edu

Fax: +82 2 825 5616