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<biogps><data><item key="platform">4</item><item key="owner">ArrayExpress Uploader</item><item key="ownerprofile_id">arrayexpress_sid</item><item key="species">human</item><item key="factors"><item><item key="GSM645710 1"/></item><item><item key="GSM645711 1"/></item><item><item key="GSM645712 1"/></item><item><item key="GSM645713 1"/></item><item><item key="GSM645714 1"/></item><item><item key="GSM645715 1"/></item><item><item key="GSM645716 1"/></item><item><item key="GSM645717 1"/></item><item><item key="GSM645718 1"/></item><item><item key="GSM645719 1"/></item><item><item key="GSM645720 1"/></item><item><item key="GSM645721 1"/></item></item><item key="id">3901</item><item key="pop_total">0</item><item key="source">http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-26298</item><item key="summary_wrapped">Under conditions of hormonal adjuvant treatment the estrogen receptor apoprotein supports breast cancer cell cycling through the retinoic...</item><item key="pubmed_id">21299862</item><item key="owner_profile">/profile/8773/arrayexpressuploader</item><item key="factor_count">0</item><item key="sample_count">12</item><item key="tags"><item>basal</item><item>breast</item><item>breast cancer</item><item>cancer</item><item>cell</item><item>estrogen</item><item>glucose</item><item>glutamine</item><item>hormone</item></item><item key="lastmodified">Dec.12, 2014</item><item key="is_default">False</item><item key="geo_gds_id"/><item key="slug">under-conditions-of-hormonal-adjuvant-treatment-th</item><item key="geo_id_plat">E-GEOD-26298_A-AFFY-44</item><item key="name">Under conditions of hormonal adjuvant treatment the estrogen receptor apoprotein supports breast cancer cell cycling through the retinoic acid receptor &#945;1 apoprotein</item><item key="created">Sep.15, 2014</item><item key="summary">Under conditions of hormonal adjuvant treatment the estrogen receptor apoprotein supports breast cancer cell cycling through the retinoic acid receptor &#945;1 apoprotein. Basal proliferation persisted in estrogen-sensitive breast cancer cells grown in hormone depleted conditioned media without or with 4-hydroxytamoxifen (OH-Tam). Downregulating ER using siRNA  inhibited basal proliferation by promoting cell cycle arrest. The basal expression of RAR&#945;1, the only RAR&#945; isoform that was expressed in breast cancer cell lines and in most breast tumors, was supported by apo-ER but was unaffected by OH-Tam. The overlapping tamoxifen-insensitive gene regulation by apo-ER and apo-RAR&#945;1 comprised activation of mainly genes promoting cell cycle and mitosis and suppression of genes involved in growth inhibition. Cells were plated at 20% confluence in low glucose phenol red free medium supplemented with 5% charcoal stripped FBS and glutamine 24h-48h prior to transfection. Treatment with vehicle, OH-Tam (100nM), or OH-Tam (500nM) was begun an additional 24h later. Cells were transfected with control siRNA, ER&#945; siRNA or RAR&#945; siRNA.</item><item key="geo_gse_id">E-GEOD-26298</item><item key="sample_source">http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-26298/samples/</item></data></biogps>
