Document Detail


Apoptosis-associated cleavage of beta-catenin in human colon cancer and rat hepatoma cells.
MedLine Citation:
PMID:  10224675     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Proteases belonging to the caspase family play a crucial role in apoptotic processes. Identification of protein cleavage specific to apoptosis may therefore provide further information about the mechanisms of apoptosis. In this study, apoptosis and necrosis were induced in cells of the human colon cancer cell lines, WiDr and DLD-1, and the resulting protein cleavage patterns investigated for beta-catenin. beta-Catenin was detected as a 92 kDa protein in control viable cells, while 65-72 kDa beta-catenin cleavage fragments were characteristically observed in apoptotic cells. These fragments were not observed in necrotic cell death. Similar apoptosis-specific beta-catenin cleavage was also demonstrated in the rat hepatoma cell line McA-RH7777, suggesting that the beta-catenin cleavage is a common event in apoptosis in various cell types. The formation of 65-72 kDa beta-catenin cleavage fragments was completely prevented by a caspase-1 inhibitor Z-VAD-CH2F and a caspase-3 inhibitor Z-DEVD-CH2F, indicating that the cleavage is associated with caspase-dependent process. Since beta-catenin is implicated in cell adhesion and signal transduction, these findings may suggest various possible roles of beta-catenin degradation in the dramatic cytoskeletal and morphological changes, as well as signaling events that accompany apoptosis.
Authors:
K Fukuda
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Publication Detail:
Type:  Journal Article    
Journal Detail:
Title:  The international journal of biochemistry & cell biology     Volume:  31     ISSN:  1357-2725     ISO Abbreviation:  Int. J. Biochem. Cell Biol.     Publication Date:    1999 Mar-Apr
Date Detail:
Created Date:  1999-06-08     Completed Date:  1999-06-08     Revised Date:  2005-11-17    
Medline Journal Info:
Nlm Unique ID:  9508482     Medline TA:  Int J Biochem Cell Biol     Country:  ENGLAND    
Other Details:
Languages:  eng     Pagination:  519-29     Citation Subset:  IM    
Affiliation:
Department of Oriental Medicine, Gifu University School of Medicine, Japan. kfukuda@cc.gifu-u.ac.jp
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MeSH Terms
Descriptor/Qualifier:
Actins / metabolism
Animals
Apoptosis*
Butyrates / pharmacology
Cadherins / metabolism
Cells, Cultured
Colonic Neoplasms / metabolism*
Cytoskeletal Proteins / metabolism*
DNA Fragmentation
Electrophoresis, Polyacrylamide Gel
Humans
Hydroxamic Acids / pharmacology
Immunoblotting
Liver Neoplasms, Experimental / metabolism*
Necrosis
Protease Inhibitors / metabolism
Rats
Time Factors
Trans-Activators*
beta Catenin
Chemical
Reg. No./Substance:
0/Actins; 0/Butyrates; 0/CTNNB1 protein, human; 0/Cadherins; 0/Catnb protein, rat; 0/Cytoskeletal Proteins; 0/Hydroxamic Acids; 0/Protease Inhibitors; 0/Trans-Activators; 0/beta Catenin; 58880-19-6/trichostatin A

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


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