Document Detail


Beta-lapachone, a quinone isolated from Tabebuia avellanedae, induces apoptosis in HepG2 hepatoma cell line through induction of Bax and activation of caspase.
MedLine Citation:
PMID:  16822200     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
The DNA topoisomerase inhibitor beta-lapachone is a quinone obtained from the bark of the lapacho tree (Tabebuia avellanedae) in South America. It has been reported to possess a wide range of pharmacological properties, and is a promising cancer chemopreventive agent. In this study, the effects of beta-lapachone on the growth of the human hepatoma cell line HepG2 were investigated. The results showed that beta-lapachone inhibits the viability of HepG2 by inducing apoptosis, as evidenced by the formation of apoptotic bodies and DNA fragmentation. Reverse transcription-polymerase chain reaction and immunoblotting results indicated that treatments of cells with beta-lapachone resulted in down-regulation of anti-apoptotic Bcl-2 and Bcl-X(L) and up-regulation of pro-apoptotic Bax expression. beta-Lapachone-induced apoptosis was associated with a proteolytic activation of caspase-3 and -9 and degradation of poly(ADP-ribose) polymerase protein. However, beta-lapachone treatment did not affect the inhibitor of apoptosis proteins family and the Fas/FasL system. Taken together, our study indicated that beta-lapachone may have potential as a chemopreventive agent for liver cancer.
Authors:
Hyun Joo Woo; Kun-Young Park; Chung-Ho Rhu; Won Ho Lee; Byung Tae Choi; Gi Young Kim; Yeong-Min Park; Yung Hyun Choi
Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't    
Journal Detail:
Title:  Journal of medicinal food     Volume:  9     ISSN:  1096-620X     ISO Abbreviation:  J Med Food     Publication Date:  2006  
Date Detail:
Created Date:  2006-07-06     Completed Date:  2006-09-29     Revised Date:  2006-11-15    
Medline Journal Info:
Nlm Unique ID:  9812512     Medline TA:  J Med Food     Country:  United States    
Other Details:
Languages:  eng     Pagination:  161-8     Citation Subset:  IM    
Affiliation:
Department of Biochemistry, Dongeui University College of Oriental Medicine, Busan, Korea.
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MeSH Terms
Descriptor/Qualifier:
Antigens, CD95 / analysis
Apoptosis / drug effects*
Carcinoma, Hepatocellular
Caspase 3
Caspase 9
Caspases / metabolism*
Cell Division / drug effects
Cell Line, Tumor
DNA Fragmentation
Enzyme Activation / drug effects
Fas Ligand Protein
Flow Cytometry
Gene Expression / drug effects
Humans
Inhibitor of Apoptosis Proteins / analysis
Liver Neoplasms
Membrane Glycoproteins / analysis
Naphthoquinones / pharmacology*
Proto-Oncogene Proteins c-bcl-2 / genetics
Reverse Transcriptase Polymerase Chain Reaction
Tabebuia / chemistry*
Tumor Necrosis Factors / analysis
bcl-2-Associated X Protein / biosynthesis*,  genetics
Chemical
Reg. No./Substance:
0/Antigens, CD95; 0/FASLG protein, human; 0/Fas Ligand Protein; 0/Inhibitor of Apoptosis Proteins; 0/Membrane Glycoproteins; 0/Naphthoquinones; 0/Proto-Oncogene Proteins c-bcl-2; 0/Tumor Necrosis Factors; 0/bcl-2-Associated X Protein; 4707-32-8/beta-lapachone; EC 3.4.22.-/CASP3 protein, human; EC 3.4.22.-/CASP9 protein, human; EC 3.4.22.-/Caspase 3; EC 3.4.22.-/Caspase 9; EC 3.4.22.-/Caspases

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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