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6,8-dihydroxy-7-methoxy-1-methyl-azafluorenone induces caspase-8- and -9-mediated apoptosis in human cancer cells.

Abstract
6,8-dihydroxy-7-methoxy-1-methyl-azafluorenone (DMMA), a purified compound from Polyalthia cerasoides roots, is cytotoxic to various cancer cell lines. The aims of this study were to demonstrate the type of cancer cell death and the mechanism(s) involved. DMMA inhibited cell growth and induced apoptotic death in human leukemic cells (HL-60, U937, MOLT-4), human breast cancer MDA-MB231 cells and human hepatocellular carcinoma HepG2 cells in a dose dependent manner, with IC50 values ranging between 20-55 muM DMMA also decreased cell viability of human peripheral blood mononuclear cells. The morphology of cancer cells induced by the compound after staining with propidium iodide and examined under a fluorescence microscope was condensed nuclei and apoptotic bodies. Mitochondrial transmembrane potential (MTP) was decreased after 24h exposure in all five types of cancer cells. DMMA-induced caspase-3, -8, and -9 activity was strongly induced in human leukemic HL-60 and MOLT-4 cells, while in U937-, MDA-MB231- and HepG2-treated cells there was partial induction of caspase. In conclusion, DMMA-induced activation of caspase-8 and -9 resulted in execution of apoptotic cell death in human leukemic HL-60 and MOLT-4 cell lines via extrinsic and intrinsic pathways.
AuthorsRatana Banjerdpongchai, Patompong Khaw-On, Chantrarat Ristee, Wilart Pompimon
JournalAsian Pacific journal of cancer prevention : APJCP (Asian Pac J Cancer Prev) Vol. 14 Issue 4 Pg. 2637-41 ( 2013) ISSN: 2476-762X [Electronic] Thailand
PMID23725188 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • 6,8-dihydroxy-7-methoxy-1-methyl-azafluorenone
  • Fluorenes
  • Caspase 8
  • Caspase 9
Topics
  • Apoptosis (drug effects)
  • Blotting, Western
  • Caspase 8 (metabolism)
  • Caspase 9 (metabolism)
  • Cell Proliferation (drug effects)
  • Enzyme Activation (drug effects)
  • Fluorenes (pharmacology)
  • Humans
  • Membrane Potential, Mitochondrial (drug effects)
  • Microscopy, Fluorescence
  • Neoplasms (drug therapy, enzymology, pathology)
  • Tumor Cells, Cultured

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