Document Detail


Period is involved in the proliferation of human pancreatic MIA-PaCa2 cancer cells by TNF-alpha.
MedLine Citation:
PMID:  18480551     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Recent studies have found alterations to clock genes in several forms of cancer. Period (Per) gene plays an important role in the circadian system, the cell cycle, the induction of apoptosis, and DNA damage. However, the functions of Per in pancreatic cancer have not yet been elucidated. Here, we show that tumor necrosis factor-alpha (TNF-alpha) suppressed the expression of both Per1 and Per3 in MIA-PaCa2 cells, a human pancreatic cancer cell line. The levels of these proteins were 10% lower in the cells treated with 10 ng/mL TNF-alpha. Cell proliferation showed a 15%, 14%, and 16% decrease at 0.4, 2.0, and 10 ng/mL of TNF-alpha, respectively. In MTS-assays, MIA-PaCa2 cells transfected with siRNA against Per1 showed a 19% reduction in proliferation. However, the knockdown of Per3 did not significantly inhibit cell proliferation. The results suggest Per1 to be involved in the inhibition of the proliferation of MIA-PaCa2 cells by TNF-alpha.
Authors:
Takahiro Suzuki; Fuyuki Sato; Jun Kondo; Yang Liu; Tomomi Kusumi; Katsumi Fujimoto; Yukio Kato; Tatsusuke Sato; Hiroshi Kijima
Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't    
Journal Detail:
Title:  Biomedical research (Tokyo, Japan)     Volume:  29     ISSN:  1880-313X     ISO Abbreviation:  Biomed. Res.     Publication Date:  2008 Apr 
Date Detail:
Created Date:  2008-05-15     Completed Date:  2008-07-16     Revised Date:  2011-04-22    
Medline Journal Info:
Nlm Unique ID:  8100317     Medline TA:  Biomed Res     Country:  Japan    
Other Details:
Languages:  eng     Pagination:  99-103     Citation Subset:  IM    
Affiliation:
Department of Pathology and Bioscience, Hirosaki University Graduate School of Medicine, Hirosaki, Japan.
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MeSH Terms
Descriptor/Qualifier:
Carcinoma, Pancreatic Ductal / metabolism,  pathology*
Cell Cycle Proteins / antagonists & inhibitors,  biosynthesis,  physiology*
Cell Line, Tumor
Cell Proliferation*
Humans
Nuclear Proteins / antagonists & inhibitors,  biosynthesis,  physiology*
Pancreatic Neoplasms / metabolism,  pathology*
Period Circadian Proteins
Transcription Factors / antagonists & inhibitors,  biosynthesis,  physiology*
Tumor Necrosis Factor-alpha / physiology*
Chemical
Reg. No./Substance:
0/Cell Cycle Proteins; 0/Nuclear Proteins; 0/PER1 protein, human; 0/PER3 protein, human; 0/Period Circadian Proteins; 0/Transcription Factors; 0/Tumor Necrosis Factor-alpha

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