Genomic analysis of rodent pulmonary tissue following bis-(2-chloroethyl) sulfide exposure
| Autor: | Matthew D. Croxton, Alfred M. Sciuto, Linda M. Dorsch, Theodore S. Moran, Alison I. Hege, Christopher S. Phillips, James F. Dillman, Albert J. Sylvester |
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| Rok vydání: | 2005 |
| Předmět: |
Male
Femoral vein Lung injury Biology Toxicology Rats Sprague-Dawley chemistry.chemical_compound Gene expression Mustard Gas medicine Animals Chemical Warfare Agents RNA Messenger Gene Lung Carcinogen Oligonucleotide Array Sequence Analysis Dose-Response Relationship Drug Reverse Transcriptase Polymerase Chain Reaction Gene Expression Profiling RNA Sulfur mustard General Medicine Genomics Genes p53 Molecular biology Rats Genes cdc medicine.anatomical_structure chemistry Biochemistry Injections Intravenous |
| Zdroj: | Chemical research in toxicology. 18(1) |
| ISSN: | 0893-228X |
| Popis: | Bis-(2-chloroethyl) sulfide (sulfur mustard, SM) is a carcinogenic alkylating agent that has been utilized as a chemical warfare agent. To understand the mechanism of SM-induced lung injury, we analyzed global changes in gene expression in a rat lung SM exposure model. Rats were injected in the femoral vein with liquid SM, which circulates directly to the pulmonary vein and then to the lung. Rats were exposed to 1, 3, or 6 mg/kg of SM, and lungs were harvested at 0.5, 1, 3, 6, and 24 h postinjection. Three biological replicates were used for each time point and dose tested. RNA was extracted from the lungs and used as the starting material for the probing of replicate oligonucleotide microarrays. The gene expression data were analyzed using principal component analysis and two-way analysis of variance to identify the genes most significantly changed across time and dose. These genes were ranked by p value and categorized based on molecular function and biological process. Computer-based data mining algorithms revealed several biological processes affected by SM exposure, including protein catabolism, apoptosis, and glycolysis. Several genes that are significantly upregulated in a dose-dependent fashion have been reported as p53 responsive genes, suggesting that cell cycle regulation and p53 activation are involved in the response to SM exposure in the lung. Thus, SM exposure induces transcriptional changes that reveal the cellular response to this potent alkylating agent. |
| Databáze: | OpenAIRE |
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