Document Detail


Quantitative proteomic analysis of human breast epithelial cells with differential telomere length.
MedLine Citation:
PMID:  17395154     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Telomeres play important functional roles in cell proliferation, cell cycle regulation, and genetic stability, in which telomere length is critical. In this study, quantitative proteome comparisons for the human breast epithelial cells with short and long telomeres (184-hTERTL vs. 184-hTERTS and 90P-hTERTL vs. 90P-hTERTS), resulting from transfection of the human telomerase reverse transcriptase (hTERT) gene, were performed using cleavable isotope-coded affinity tags. More than 2000 proteins were quantified in each comparative experiment, with approximately 77% of the proteins identified in both analyses. In the cells with long telomeres, significant and consistent alterations were observed in metabolism (amino acid, nucleotide, and lipid metabolism), genetic information transmission (transcription and translation regulation, spliceosome and ribosome complexes), and cell signaling. Interestingly, the DNA excision repair pathway is enhanced, while integrin and its ligands are downregulated in the cells with long telomeres. These results may provide valuable information related to telomere functions.
Authors:
Li-Rong Yu; King C Chan; Hidetoshi Tahara; David A Lucas; Koushik Chatterjee; Haleem J Issaq; Timothy D Veenstra
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Publication Detail:
Type:  Journal Article; Research Support, N.I.H., Extramural     Date:  2007-03-22
Journal Detail:
Title:  Biochemical and biophysical research communications     Volume:  356     ISSN:  0006-291X     ISO Abbreviation:  Biochem. Biophys. Res. Commun.     Publication Date:  2007 May 
Date Detail:
Created Date:  2007-04-11     Completed Date:  2007-06-28     Revised Date:  2009-11-18    
Medline Journal Info:
Nlm Unique ID:  0372516     Medline TA:  Biochem Biophys Res Commun     Country:  United States    
Other Details:
Languages:  eng     Pagination:  942-7     Citation Subset:  IM    
Affiliation:
Laboratory of Proteomics and Analytical Technologies, SAIC-Frederick, Inc., NCI-Frederick, Frederick, Maryland 21702, USA. lyu@ncifcrf.gov
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MeSH Terms
Descriptor/Qualifier:
Breast / metabolism*,  ultrastructure
Cell Line
DNA Repair / physiology*
Epithelial Cells / metabolism*,  ultrastructure
Humans
Proteome / metabolism*
Telomere / physiology*,  ultrastructure
Grant Support
ID/Acronym/Agency:
N01 CO12400/CO/NCI/CO/NCI NIH HHS; N01-CO-12400/CO/NCI NIH HHS
Chemical
Reg. No./Substance:
0/Proteome
Comments/Corrections

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