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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="GSM1340088"><item key="TREATMENT">2 &#239;&#191;&#189;M Cmp302 for 8 h</item><item key="INFECTION">pBabe-Twist retrovirus</item></item></item><item><item key="GSM1340087"><item key="TREATMENT">2 &#239;&#191;&#189;M Cmp302 for 4 h</item><item key="INFECTION">pBabe-Twist retrovirus</item></item></item><item><item key="GSM1340086"><item key="TREATMENT">DMSO</item><item key="INFECTION">pBabe-Twist retrovirus</item></item></item><item><item key="GSM1340085"><item key="TREATMENT">2 &#239;&#191;&#189;M Cmp302 for 8 h</item><item key="INFECTION">pBabe-shGFP retrovirus</item></item></item><item><item key="GSM1340084"><item key="TREATMENT">2 &#239;&#191;&#189;M Cmp302 for 4 h</item><item key="INFECTION">pBabe-shGFP retrovirus</item></item></item><item><item key="GSM1340083"><item key="TREATMENT">DMSO</item><item key="INFECTION">pBabe-shGFP retrovirus</item></item></item></item><item key="id">2073</item><item key="pop_total">0</item><item key="platform">4</item><item key="summary_wrapped">Carcinoma cells can acquire key malignant traits by reprogramming their differentiation state via an epithelial-to-mesenchymal transition...</item><item key="pubmed_id">24705811</item><item key="geo_gse_id">E-GEOD-55604</item><item key="owner_profile">/profile/8773/arrayexpressuploader</item><item key="factor_count">2</item><item key="sample_count">6</item><item key="tags"><item>cancer</item><item>carcinoma</item></item><item key="lastmodified">Dec.12, 2014</item><item key="is_default">False</item><item key="geo_id_plat">E-GEOD-55604_A-AFFY-44</item><item key="slug">a-novel-emt-selective-small-molecule-induces-er-st</item><item key="geo_gds_id"/><item key="name">A novel EMT-selective small molecule induces ER stress</item><item key="created">Jul.11, 2014</item><item key="summary">Carcinoma cells can acquire key malignant traits by reprogramming their differentiation state via an epithelial-to-mesenchymal transition (EMT). Cancer cells that undergo EMT become invasive and resist a wide range of therapies including most chemotherapy drugs and radiation.  Such cells are also able to efficiently seed primary and metastatic tumors, making them functionally indistinguishable from tumor-initiating or cancer stem-like cells (TICs or CSCs). Therefore, there is significant interest in finding vulnerabilities of cancer cells that have undergone EMT. A potent EMT-selective small molecule was discovered through a large-scale chemical screen. We used microarray analysis to understand the biological effects of this compound. HMLE_ctrl (human MECs, infected with a pBabe-shGFP retrovirus) and HMLE_Twist (human MECs, infected with a pBabe-Twist retrovirus) cells were treated with solvent control (DMSO), 5 &#181;M or 10 &#181;M of Cmp302 for 6 hours. Microarray analysis was performed to profile global gene expression.</item><item key="source">http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-55604</item><item key="sample_source">http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-55604/samples/</item></data></biogps>
