<HashMap><database>biostudies-other</database><scores/><additional><submitter>Nickols NG</submitter><pagination>561-571</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-ECPF-GEOD-7835</full_dataset_link><project>EurocanPlatform</project><abstract>Transcription mediated by hypoxia inducible factor (HIF-1) contributes to tumor angiogenesis and metastasis but is also involved in the activation of cell-death pathways and normal physiological processes.  Given the complexity of HIF-1 signaling it could be advantageous to target a subset of HIF-1 effectors rather than the entire pathway.  We compared the genome-wide effects of three molecules that each interfere with the HIF-1-DNA interaction: a polyamide targeted to the hypoxia response element (HRE), siRNA targeted to HIF-1α, and echinomycin, a DNA binding natural product with a similar but less specific sequence preference to the polyamide.  The polyamide affects a subset of hypoxia-induced genes that are consistent with the binding site preferences of the polyamide.  For comparison, </abstract><repository>biostudies-other</repository><experiment_type>transcription profiling by array</experiment_type><data_source>EurocanPlatform</data_source><omics_type>Unknown</omics_type><volume>2</volume><journal>ACS chemical biology</journal><species>Homo sapiens</species><pubmed_authors>Farkas ME</pubmed_authors><pubmed_authors>Nickols NG</pubmed_authors><pubmed_authors>Jacobs CS</pubmed_authors><pubmed_authors>Dervan PB</pubmed_authors></additional><is_claimable>false</is_claimable><name>Transcription profiling by array of human glioblastoma cells after stimulation with deferoxamine and treatment with polyamide 1, echinomycin, or HIF-1a siRNA</name><description>Transcription mediated by hypoxia inducible factor (HIF-1) contributes to tumor angiogenesis and metastasis but is also involved in the activation of cell-death pathways and normal physiological processes.  Given the complexity of HIF-1 signaling it could be advantageous to target a subset of HIF-1 effectors rather than the entire pathway.  We compared the genome-wide effects of three molecules that each interfere with the HIF-1-DNA interaction: a polyamide targeted to the hypoxia response element (HRE), siRNA targeted to HIF-1α, and echinomycin, a DNA binding natural product with a similar but less specific sequence preference to the polyamide.  The polyamide affects a subset of hypoxia-induced genes that are consistent with the binding site preferences of the polyamide.  For comparison, </description><dates><release>2016-04-14T14:43:35Z</release><publication>2007 Aug</publication><modification>2016-04-14T14:43:35Z</modification><creation>2016-04-14T14:43:35Z</creation></dates><accession>S-ECPF-GEOD-7835</accession><cross_references><GEO>GSE7835</GEO><ArrayExpress>E-GEOD-7835</ArrayExpress><EFO>EFO_0000322</EFO><EFO>EFO_0000519</EFO><ArrayExpress files>E-GEOD-7835</ArrayExpress files></cross_references></HashMap>