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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="GSM437517"><item key="PIR KNOCK-DOWN">yes</item></item></item><item><item key="GSM437517"><item key="PIR KNOCK-DOWN">yes</item></item></item><item><item key="GSM437519"><item key="PIR KNOCK-DOWN">no</item></item></item><item><item key="GSM437519"><item key="PIR KNOCK-DOWN">no</item></item></item><item><item key="GSM437519"><item key="PIR KNOCK-DOWN">no</item></item></item><item><item key="GSM437519"><item key="PIR KNOCK-DOWN">no</item></item></item></item><item key="id">3383</item><item key="ownerprofile_id">arrayexpress_sid</item><item key="platform">4</item><item key="summary_wrapped">Pirin (PIR) is a putative transcriptional regulator abundantly expressed in melanocytes and in a subset of primary and metastatic...</item><item key="geo_gse_id">E-GEOD-17551</item><item key="owner_profile">/profile/8773/arrayexpressuploader</item><item key="factor_count">1</item><item key="sample_count">6</item><item key="tags"><item>cell</item><item>melanoma</item><item>metastatic melanoma</item></item><item key="lastmodified">Dec.12, 2014</item><item key="is_default">False</item><item key="geo_gds_id"/><item key="slug">genes-regulated-after-transient-knock-down-of-piri</item><item key="geo_id_plat">E-GEOD-17551_A-AFFY-44</item><item key="name">Genes regulated after transient knock-down of Pirin in WM-266 cells</item><item key="created">Sep.12, 2014</item><item key="summary">Pirin (PIR) is a putative transcriptional regulator abundantly expressed in melanocytes and in a subset of primary and metastatic melanomas. Ablation of PIR in the melanoma cell lines results in induction of a senescence-like phenotype.  Keywords: Transcriptional regulation, knock-down using siRNA We analyzed gene expression profiles of WM-266.4 metastatic melanoma cells after knock-down of PIR, which was achieved using a pool of four PIR-siRNA duplexes (siPIR). A pool of four non-targeting siRNA duplexes was used as control of off-target transcriptional effects (siCTR). Cells that underwent transfection with no oligonucleotides (oligofectamine only) were also included to measure all non-specific effects (NO cells). For each sample, an RNA pool was obtained by mixing equal quantities of total RNA from each of three independent RNA extractions. Each biotin-labeled target was hybridized to two GeneChip HG-U133 Plus v.2 arrays.</item><item key="source">http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-17551</item><item key="sample_source">http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-17551/samples/</item></data></biogps>
