<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Saban MR</submitter><funding>NIDDK NIH HHS</funding><pagination>4</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC2262873</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>9</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>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 </pubmed_abstract><journal>BMC immunology</journal><pubmed_title>Molecular networks discriminating mouse bladder responses to intravesical bacillus Calmette-Guerin (BCG), LPS, and TNF-alpha.</pubmed_title><pmcid>PMC2262873</pmcid><funding_grant_id>5 R01 DK066101-02</funding_grant_id><funding_grant_id>R01 DK066101</funding_grant_id><funding_grant_id>R01 DK069808</funding_grant_id><funding_grant_id>R01 DK055828</funding_grant_id><funding_grant_id>R21 DK062889</funding_grant_id><funding_grant_id>5 R01 DK055828-05</funding_grant_id><pubmed_authors>O'Donnell MA</pubmed_authors><pubmed_authors>Hurst RE</pubmed_authors><pubmed_authors>Wu XR</pubmed_authors><pubmed_authors>Saban MR</pubmed_authors><pubmed_authors>Simpson C</pubmed_authors><pubmed_authors>Dozmorov I</pubmed_authors><pubmed_authors>Davis C</pubmed_authors><pubmed_authors>Saban R</pubmed_authors></additional><is_claimable>false</is_claimable><name>Molecular networks discriminating mouse bladder responses to intravesical bacillus Calmette-Guerin (BCG), LPS, and TNF-alpha.</name><description>&lt;h4>Background&lt;/h4>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 </description><dates><release>2008-01-01T00:00:00Z</release><publication>2008 Feb</publication><modification>2026-05-05T04:06:31.276Z</modification><creation>2019-03-27T02:44:16Z</creation></dates><accession>S-EPMC2262873</accession><cross_references><pubmed>18267009</pubmed><doi>10.1186/1471-2172-9-4</doi></cross_references></HashMap>