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<biogps><data><item key="owner">ArrayExpress Uploader</item><item key="pop_total">0</item><item key="id">8846</item><item key="factors"><item><item key="GSE9727GSM245903"/></item><item><item key="GSE9727GSM245904"/></item><item><item key="GSE9727GSM245905"/></item><item><item key="GSE9727GSM245897"/></item><item><item key="GSE9727GSM245898"/></item><item><item key="GSE9727GSM245899"/></item><item><item key="GSE9727GSM245900"/></item><item><item key="GSE9727GSM245901"/></item><item><item key="GSE9727GSM245902"/></item><item><item key="GSE9727GSM245893"/></item><item><item key="GSE9727GSM245894"/></item><item><item key="GSE9727GSM245895"/></item><item><item key="GSE9727GSM245896"/></item><item><item key="GSE9727GSM248228"/></item><item><item key="GSE9727GSM248229"/></item><item><item key="GSE9727GSM248230"/></item><item><item key="GSE9727GSM248222"/></item><item><item key="GSE9727GSM248223"/></item><item><item key="GSE9727GSM248224"/></item><item><item key="GSE9727GSM248225"/></item><item><item key="GSE9727GSM248226"/></item><item><item key="GSE9727GSM248227"/></item><item><item key="GSE9727GSM248218"/></item><item><item key="GSE9727GSM248219"/></item><item><item key="GSE9727GSM248220"/></item><item><item key="GSE9727GSM248221"/></item></item><item key="ownerprofile_id">arrayexpress_sid</item><item key="platform">8</item><item key="summary_wrapped">The second messenger cAMP acts via protein kinase A (PKA) to induce apoptosis by mechanisms that are poorly understood. Here, we assessed...</item><item key="pubmed_id">18048352</item><item key="geo_gse_id">E-GEOD-9727</item><item key="owner_profile">/profile/8773/arrayexpressuploader</item><item key="factor_count">0</item><item key="sample_count">26</item><item key="tags"><item>cell</item><item>lymphoma</item><item>membrane</item><item>protein</item></item><item key="lastmodified">Dec.12, 2014</item><item key="is_default">False</item><item key="geo_gds_id"/><item key="slug">transcription-profiling-of-mouse-s49-lymphoma-cell</item><item key="geo_id_plat">E-GEOD-9727_A-AFFY-36</item><item key="name">Transcription profiling of mouse S49 lymphoma cell deathless (D-) cell variant</item><item key="created">Nov.24, 2014</item><item key="summary">The second messenger cAMP acts via protein kinase A (PKA) to induce apoptosis by mechanisms that are poorly understood. Here, we assessed a role for mitochondria and analyzed gene expression in cAMP/PKA-promoted apoptosis by comparing wild-type (WT) S49 lymphoma cells and the S49 variant, D- (cAMP-deathless), which lacks cAMP-promoted apoptosis but has wild-type levels of PKA activity and cAMP-promoted G1 growth arrest. Treatment of WT, but not D-, S49 cells with 8-CPT-cAMP for 24 h induced loss of mitochondrial membrane potential, mitochondrial release of cytochrome c and Smac and increase in caspase-3 activity. Gene expression analysis (using Affymetrix 430 2.0  Arrays) revealed that WT and D- cells incubated with 8-CPT-cAMP have similar, but non-identical, extents of cAMP-regulated gene expression at 2h (~800 transcripts) and 6h (~1000 transcripts) (|Fold|&gt;2, P&lt;0.06); by contrast, at 24h ~2500 and ~1100 transcripts were changed in WT and D- cells, respectively. Using an approach that combined regression analysis, clustering and functional annotation to identify transcripts that showed differential expression between WT and D- cells, we found differences in cAMP-mediated regulation of mRNAs involved in transcriptional repression, apoptosis, the cell cycle, RNA splicing, Golgi and lysosomes. The 2 cell lines differed in CREB phosphorylation and expression of the transcriptional inhibitor Icer and in cAMP-regulated expression of genes in the Inhibitor of apoptosis (IAP) and Bcl families. The findings indicate that cAMP/PKA-promoted apoptosis of lymphoid cells occurs via mitochondrial-mediated events and imply that such apoptosis involves gene networks in multiple biochemical pathways. Experiment Overall Design: S49 D- cells were treated with 8-CPT-cAMP over the course of 24 hours. Cells were prepared for hybridization to microarrays at times 0-untreated, 2h, 6h, and 24h after treatment with 8-CPT-cAMP. Experimental replicates were as follows n=4 for time 0 and n=3 for 2, 6, and 24h post treatment.</item><item key="source">http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-9727</item><item key="species">mouse</item><item key="sample_source">http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-9727/samples/</item></data></biogps>
