Document Detail


Interference with 3',5'-cyclic adenosine monophosphate response element binding protein stimulates apoptosis through aberrant cell cycle progression and checkpoint activation.
MedLine Citation:
PMID:  16410315     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
We previously reported that protein kinase A activity is an important determinant of thyroid cell survival. Given the important role of cAMP response element binding protein (CREB) in mediating the transcriptional effects of protein kinase A, we explored whether interference with CREB family members impaired thyroid cell survival. Expression of A-CREB, a dominant-negative CREB mutant that inhibits CREB DNA binding activity, induced apoptosis in rat thyroid cells. A-CREB inhibited CRE-regulated gene expression but failed to alter the expression of bcl-2 family members or of well-characterized inhibitors of apoptosis. To elucidate the mechanism through which impaired CREB function triggered apoptosis, its effects on cell proliferation were examined. Expression of A-CREB inhibited cell number increases, in part due to delayed cell cycle transit. Protracted S-phase progression in A-CREB-expressing cells was sufficient to activate a checkpoint response characterized by Chk-1, histone H2A.X, and p53 phosphorylation. To determine whether cell cycle progression was required for apoptosis, the effects of p27 overexpression were investigated. Overexpression of p27 prevented cell cycle progression, checkpoint activation, and apoptosis in A-CREB-expressing cells. These data reveal a novel mechanism through which interference with CREB abrogates cell survival, through checkpoint activation secondary to cell cycle delay. This study may explain how interference with CREB induces apoptosis in cells where alterations in the expression of pro- and anti-survival genes are not detected.
Authors:
Jessica H Dworet; Judy L Meinkoth
Related Documents :
9167765 - Apoptotic program is initiated but not completed in lncap cells in response to growth i...
12632065 - Inhibited proliferation of cyclooxygenase-2 expressing human hepatoma cells by ns-398, ...
20470875 - Protective effects of gastrodia elata blume on mpp+-induced cytotoxicity in human dopam...
11292165 - Bcl-2 and bax expression in cartilage and bone cells after high-dose corticosterone tre...
23669265 - Preparation of novel antiproliferative emodin derivatives and studies on their cell cyc...
24588135 - Cephalochromin induces g0/g1 cell cycle arrest and apoptosis in a549 human non-small-ce...
Publication Detail:
Type:  Journal Article; Research Support, N.I.H., Extramural     Date:  2006-01-12
Journal Detail:
Title:  Molecular endocrinology (Baltimore, Md.)     Volume:  20     ISSN:  0888-8809     ISO Abbreviation:  Mol. Endocrinol.     Publication Date:  2006 May 
Date Detail:
Created Date:  2006-05-02     Completed Date:  2006-07-31     Revised Date:  2011-11-02    
Medline Journal Info:
Nlm Unique ID:  8801431     Medline TA:  Mol Endocrinol     Country:  United States    
Other Details:
Languages:  eng     Pagination:  1112-20     Citation Subset:  IM    
Affiliation:
Department of Pharmacology, University of Pennsylvania School of Medicine, 420 Curie Boulevard, Philadelphia, Pennsylvania 19104-6061, USA.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:
Animals
Apoptosis* / genetics
Cell Cycle* / genetics
Cells, Cultured
Cyclic AMP Response Element-Binding Protein / antagonists & inhibitors*,  genetics,  physiology
Cyclin-Dependent Kinase Inhibitor p27 / metabolism
Gene Expression
Histones / metabolism
Protein Kinases / metabolism*
Rats
Rats, Wistar
Recombinant Fusion Proteins / genetics,  metabolism
Thyroid Gland / cytology,  metabolism
Tumor Suppressor Protein p53 / metabolism
Grant Support
ID/Acronym/Agency:
DK45696/DK/NIDDK NIH HHS; DK55757/DK/NIDDK NIH HHS
Chemical
Reg. No./Substance:
0/A-CREB protein; 0/Cyclic AMP Response Element-Binding Protein; 0/Histones; 0/Recombinant Fusion Proteins; 0/Tumor Suppressor Protein p53; 147604-94-2/Cyclin-Dependent Kinase Inhibitor p27; EC 2.7.-/Protein Kinases; EC 2.7.11.1/Checkpoint kinase 1

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


Previous Document:  Involvement of IL-32 in activation-induced cell death in T cells.
Next Document:  p38 mitogen-activated protein kinase stimulates estrogen-mediated transcription and proliferation th...