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<biogps><data><item key="owner">ArrayExpress Uploader</item><item key="ownerprofile_id">arrayexpress_sid</item><item key="species">human</item><item key="factors"><item><item key="GSM1098984"><item key="TREATMENT">450mg/kg AGI-5198</item></item></item><item><item key="GSM1098984"><item key="TREATMENT">450mg/kg AGI-5198</item></item></item><item><item key="GSM1098984"><item key="TREATMENT">450mg/kg AGI-5198</item></item></item><item><item key="GSM1098984"><item key="TREATMENT">450mg/kg AGI-5198</item></item></item><item><item key="GSM1098984"><item key="TREATMENT">450mg/kg AGI-5198</item></item></item><item><item key="GSM1098984"><item key="TREATMENT">450mg/kg AGI-5198</item></item></item><item><item key="GSM1098984"><item key="TREATMENT">450mg/kg AGI-5198</item></item></item><item><item key="GSM1098977"><item key="TREATMENT">150mg/kg AGI-5198</item></item></item><item><item key="GSM1098977"><item key="TREATMENT">150mg/kg AGI-5198</item></item></item><item><item key="GSM1098977"><item key="TREATMENT">150mg/kg AGI-5198</item></item></item><item><item key="GSM1098977"><item key="TREATMENT">150mg/kg AGI-5198</item></item></item><item><item key="GSM1098977"><item key="TREATMENT">150mg/kg AGI-5198</item></item></item><item><item key="GSM1098977"><item key="TREATMENT">150mg/kg AGI-5198</item></item></item><item><item key="GSM1098977"><item key="TREATMENT">150mg/kg AGI-5198</item></item></item><item><item key="GSM1098977"><item key="TREATMENT">150mg/kg AGI-5198</item></item></item><item><item key="GSM1098969"><item key="TREATMENT">vehicle</item></item></item><item><item key="GSM1098969"><item key="TREATMENT">vehicle</item></item></item><item><item key="GSM1098969"><item key="TREATMENT">vehicle</item></item></item><item><item key="GSM1098969"><item key="TREATMENT">vehicle</item></item></item><item><item key="GSM1098969"><item key="TREATMENT">vehicle</item></item></item><item><item key="GSM1098969"><item key="TREATMENT">vehicle</item></item></item><item><item key="GSM1098969"><item key="TREATMENT">vehicle</item></item></item><item><item key="GSM1098969"><item key="TREATMENT">vehicle</item></item></item><item><item key="GSM1098969"><item key="TREATMENT">vehicle</item></item></item><item><item key="GSM1098960"><item key="TREATMENT">AGI-5198</item></item></item><item><item key="GSM1098969"><item key="TREATMENT">vehicle</item></item></item><item><item key="GSM1098960"><item key="TREATMENT">AGI-5198</item></item></item><item><item key="GSM1098969"><item key="TREATMENT">vehicle</item></item></item><item><item key="GSM1098969"><item key="TREATMENT">vehicle</item></item></item><item><item key="GSM1098960"><item key="TREATMENT">AGI-5198</item></item></item><item><item key="GSM1098960"><item key="TREATMENT">AGI-5198</item></item></item><item><item key="GSM1098960"><item key="TREATMENT">AGI-5198</item></item></item><item><item key="GSM1098969"><item key="TREATMENT">vehicle</item></item></item></item><item key="id">2477</item><item key="pop_total">0</item><item key="platform">4</item><item key="summary_wrapped">The recent discovery of mutations in metabolic enzymes has rekindled interest in harnessing the altered metabolism of cancer cells for...</item><item key="geo_gse_id">E-GEOD-45197</item><item key="owner_profile">/profile/8773/arrayexpressuploader</item><item key="factor_count">1</item><item key="sample_count">33</item><item key="tags"><item>cancer</item><item>genome</item><item>glioma</item><item>histone</item></item><item key="lastmodified">Dec.12, 2014</item><item key="is_default">False</item><item key="geo_gds_id"/><item key="slug">an-inhibitor-of-mutant-idh1-delays-growth-and-prom</item><item key="geo_id_plat">E-GEOD-45197_A-AFFY-44</item><item key="name">An Inhibitor of Mutant IDH1 Delays Growth and Promotes Differentiation of Glioma Cells Expression data for Xenograft Samples</item><item key="created">Jul.12, 2014</item><item key="summary">The recent discovery of mutations in metabolic enzymes has rekindled interest in harnessing the altered metabolism of cancer cells for cancer therapy. One potential drug target is isocitrate dehydrogenase 1 (IDH1) which is mutated in multiple human cancers. Here, we examine the role of mutant IDH1 in fully transformed cells with endogenous IDH1 mutations. A selective R132H-IDH1 inhibitor (AGI-5198) identified through a high-throughput screen dose-dependently blocked the ability of the mutant enzyme (mIDH1) to produce R-2-hydroxyglutarate (R-2HG). Under conditions of near complete R-2HG inhibition, the mIDH1 inhibitor induced demethylation of histone H3K9M3 and expression of genes associated with gliogenic differentiation. Blockade of mIDH1 impaired the growth of IDH1-mutant - but not IDH1-wildtype &#8211; glioma cells without appreciable changes in genome wide DNA methylation. These data suggest that mIDH1 may promote glioma growth through mechanisms beyond its well-characterized epigenetic effects. Two xenograft experiments were carried out, one with treatment cohorts of vehicle and 450mg/kg, and the other with vehicle, 150mg/kg/day, and 450mg/kg/day. After the indicated time tumors were harvested and total RNA was extracted and analyzed by the Affymetrix U133 plus 2 array.</item><item key="source">http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-45197</item><item key="sample_source">http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-45197/samples/</item></data></biogps>
