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Status |
Public on Aug 24, 2005 |
Title |
Identification of novel transcriptional networks in response to the treatment D3T (3H-1, 2-dithiole-3-thione) |
Organism |
Rattus norvegicus |
Experiment type |
Expression profiling by array
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Summary |
3H-1, 2-dithiole-3-thione (D3T), an inducer of antioxidant and phase 2 genes, is known to enhance the detoxification of environmental carcinogens, prevent neoplasia, and to elicit other protective effects. However, a comprehensive view of the regulatory pathways induced by this compound has not yet been elaborated. Fischer F344 rats were gavaged daily for 5 days with vehicle or D3T (0.3 mmol/kg). The global changes of gene expression in liver were measured with Affymetrix RG-U34A chips. Using functional class scoring, a semi-supervised method exploring both the expression pattern and the functional annotation of the genes, the Gene Ontology classes were ranked according to the significance of the impact of D3T treatment. Two unexpected functional classes were identified for the D3T treatment, cytosolic ribosome constituents with 90% of those genes increased, and cholesterol biosynthesis with 91% of the genes repressed. In another novel approach, the differentially expressed genes were evaluated by the Ingenuity computational pathway analysis tool to identify specific regulatory networks and canonical pathways responsive to D3T treatment. In addition to the known glutathione metabolism pathway (ρ = 0.0011), several other significant pathways were also revealed, including antigen presentation (ρ = 0.000476), androgen/estrogen biosynthesis (ρ = 0.000551), fatty acid (ρ = 0.000216) and tryptophan metabolism (ρ = 0.000331) pathways. These findings showed a profound impact of D3T on lipid metabolism and anti-inflammatory/immune-suppressive response, indicating broader cytoprotective effect of this compound than previously expected. Keywords: Response to antioxidant compound
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Overall design |
Total RNA were isolated from either vehicle or D3T (0.3mmol/kg body weight) treated rat liver, 4 rats for each group, hybridized on 8 Affymetrix RG-U34A chips
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Contributor(s) |
Huang Y, Yan J, Lubet R, Kensler TW, Sutter TR |
Citation(s) |
16317079 |
Submission date |
Aug 22, 2005 |
Last update date |
Feb 21, 2017 |
Contact name |
Yong Huang |
E-mail(s) |
yh9fj@virginia.edu
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Phone |
(434) 243-0842
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Organization name |
University of Viginia
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Department |
Medicine
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Street address |
1340 Jefferson Park Ave
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City |
Charlottesville |
State/province |
VA |
ZIP/Postal code |
22908 |
Country |
USA |
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Platforms (1) |
GPL85 |
[RG_U34A] Affymetrix Rat Genome U34 Array |
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Samples (8)
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Relations |
BioProject |
PRJNA92715 |
Supplementary data files not provided |
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