| pubmed-article:18267009 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:18267009 | lifeskim:mentions | umls-concept:C1882071 | lld:lifeskim |
| pubmed-article:18267009 | lifeskim:mentions | umls-concept:C0085957 | lld:lifeskim |
| pubmed-article:18267009 | lifeskim:mentions | umls-concept:C0025914 | lld:lifeskim |
| pubmed-article:18267009 | lifeskim:mentions | umls-concept:C0026809 | lld:lifeskim |
| pubmed-article:18267009 | lifeskim:mentions | umls-concept:C2697656 | lld:lifeskim |
| pubmed-article:18267009 | lifeskim:mentions | umls-concept:C0005682 | lld:lifeskim |
| pubmed-article:18267009 | lifeskim:mentions | umls-concept:C0175697 | lld:lifeskim |
| pubmed-article:18267009 | lifeskim:mentions | umls-concept:C0023810 | lld:lifeskim |
| pubmed-article:18267009 | lifeskim:mentions | umls-concept:C1456820 | lld:lifeskim |
| pubmed-article:18267009 | lifeskim:mentions | umls-concept:C1704632 | lld:lifeskim |
| pubmed-article:18267009 | lifeskim:mentions | umls-concept:C0871261 | lld:lifeskim |
| pubmed-article:18267009 | lifeskim:mentions | umls-concept:C1521991 | lld:lifeskim |
| pubmed-article:18267009 | lifeskim:mentions | umls-concept:C2911692 | lld:lifeskim |
| pubmed-article:18267009 | lifeskim:mentions | umls-concept:C1706817 | lld:lifeskim |
| pubmed-article:18267009 | lifeskim:mentions | umls-concept:C0442124 | lld:lifeskim |
| pubmed-article:18267009 | pubmed:dateCreated | 2008-3-5 | lld:pubmed |
| pubmed-article:18267009 | pubmed:abstractText | Despite being a mainstay for treating superficial bladder carcinoma and a promising agent for interstitial cystitis, the precise mechanism of Bacillus Calmette-Guerin (BCG) remains poorly understood. It is particularly unclear whether BCG is capable of altering gene expression in the bladder target organ beyond its well-recognized pro-inflammatory effects and how this relates to its therapeutic efficacy. The objective of this study was to determine differentially expressed genes in the mouse bladder following chronic intravesical BCG therapy and to compare the results to non-specific pro inflammatory stimuli (LPS and TNF-alpha). For this purpose, C57BL/6 female mice received four weekly instillations of BCG, LPS, or TNF-alpha. Seven days after the last instillation, the urothelium along with the submucosa was removed from detrusor muscle and the RNA was extracted from both layers for cDNA array experiments. Microarray results were normalized by a robust regression analysis and only genes with an expression above a conditional threshold of 0.001 (3SD above background) were selected for analysis. Next, genes presenting a 3-fold ratio in regard to the control group were entered in Ingenuity Pathway Analysis (IPA) for a comparative analysis in order to determine genes specifically regulated by BCG, TNF-alpha, and LPS. In addition, the transcriptome was precipitated with an antibody against RNA polymerase II and real-time polymerase chain reaction assay (Q-PCR) was used to confirm some of the BCG-specific transcripts. | lld:pubmed |
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| pubmed-article:18267009 | pubmed:language | eng | lld:pubmed |
| pubmed-article:18267009 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:18267009 | pubmed:citationSubset | IM | lld:pubmed |
