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<biogps><data><item key="owner">ArrayExpress Uploader</item><item key="pop_total">0</item><item key="species">human</item><item key="factors"><item><item key="GSM97818"><item key="PROTOCOL">ethanol treated cells (vehicle) 3h</item></item></item><item><item key="GSM978182"><item key="PROTOCOL">estradiol treated cells 3h</item></item></item><item><item key="GSM978183"><item key="PROTOCOL">ER&#945;17p treated cells 3h</item></item></item></item><item key="id">4540</item><item key="ownerprofile_id">arrayexpress_sid</item><item key="platform">4</item><item key="summary_wrapped">ER&#945;17p is a synthetic peptide corresponding to the sequence P295LMIKRSKKNSLALSLT311 of the estrogen receptor alpha (ER&#945;) and initially...</item><item key="geo_gse_id">E-GEOD-39720</item><item key="owner_profile">/profile/8773/arrayexpressuploader</item><item key="factor_count">1</item><item key="sample_count">3</item><item key="tags"><item>actin</item><item>breast</item><item>breast cancer</item><item>calmodulin</item><item>cancer</item><item>cell</item><item>estrogen</item><item>line</item></item><item key="lastmodified">Dec.12, 2014</item><item key="is_default">False</item><item key="geo_gds_id"/><item key="slug">time-course-effect-of-estradiol-and-era17p-on-ea-2</item><item key="geo_id_plat">E-GEOD-39720_A-AFFY-44</item><item key="name">Time-course effect of estradiol and ERa17p on Early Gene expression in T47D cells</item><item key="created">Sep.19, 2014</item><item key="summary">ER&#945;17p is a synthetic peptide corresponding to the sequence P295LMIKRSKKNSLALSLT311 of the estrogen receptor alpha (ER&#945;) and initially synthesized to mimic its calmodulin binding site. ER&#945;17p was subsequently found to elicit estrogenic responses in E2-deprived ER&#945;-positive breast cancer cells, increasing proliferation and E2-dependent gene transcription.  Surprisingly, in E2-supplemented media, ER&#945;17p induced apoptosis and modified the actin network, influencing thereby cell motility. Here, we report that ER&#945;17p induces a massive early (3h) transcriptional activity in breast cancer cell line T47D. Cells after a 4h incubation with medium containing 10% charcoal stripped FBS were incubated with or without E2 (10-6M) or ERa17p in RPMI 1640 supplemented with 10% charcoal stripped FBS, for 3 hours. Total RNA was isolated using Nucleospin II columns (Macheray-Nagel, Dttren, Germany), according to the manufacturer&#8217;s instructions. RNA was labeled and hybridized according to the Affymetrix protocol (Affymetrix Gene-Chip Expression Analysis Technical Manual), using the HGU133A plus 2 chip, analyzing a total of 54675 transcripts. Signals were detected by an Affymetrix microarray chip reader.</item><item key="source">http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-39720</item><item key="sample_source">http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-39720/samples/</item></data></biogps>
