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<biogps><data><item key="owner">ArrayExpress Uploader</item><item key="ownerprofile_id">arrayexpress_sid</item><item key="species">mouse</item><item key="factors"><item><item key="GSM684317"><item key="GROUP">Lgr5 High</item><item key="HYBRIDIZATION_DATE">April_2010</item></item></item><item><item key="GSM684318"><item key="GROUP">Lgr5 Low</item><item key="HYBRIDIZATION_DATE">April_2010</item></item></item><item><item key="GSM684319"><item key="GROUP">EphB2 High</item><item key="HYBRIDIZATION_DATE">Feb_2009</item></item></item><item><item key="GSM684320"><item key="GROUP">EphB2 Medium</item><item key="HYBRIDIZATION_DATE">Feb_2009</item></item></item><item><item key="GSM68432"><item key="GROUP">EphB2 Low</item><item key="HYBRIDIZATION_DATE">Feb_2009</item></item></item><item><item key="GSM684322"><item key="GROUP">EphB2 High</item><item key="HYBRIDIZATION_DATE">March_2009</item></item></item><item><item key="GSM684323"><item key="GROUP">EphB2 Medium</item><item key="HYBRIDIZATION_DATE">March_2009</item></item></item><item><item key="GSM684324"><item key="GROUP">EphB2 Low</item><item key="HYBRIDIZATION_DATE">March_2009</item></item></item></item><item key="id">6379</item><item key="pop_total">0</item><item key="platform">6</item><item key="summary_wrapped">Using EphB2 or the ISC marker Lgr5, we have FACS-purified and profiled intestinal stem cells (ISCs), crypt proliferative progenitors and...</item><item key="geo_gse_id">E-GEOD-27605</item><item key="owner_profile">/profile/8773/arrayexpressuploader</item><item key="factor_count">2</item><item key="sample_count">8</item><item key="tags"><item>cancer</item><item>cell</item><item>colorectal cancer</item><item>disease</item><item>stem cell</item></item><item key="lastmodified">Dec.12, 2014</item><item key="is_default">False</item><item key="geo_id_plat">E-GEOD-27605_A-AFFY-45</item><item key="slug">the-intestinal-stem-cell-signature-identifies-colo</item><item key="geo_gds_id"/><item key="name">The intestinal stem cell signature identifies colorectal cancer stem cells and predicts disease relapse</item><item key="created">Nov.11, 2014</item><item key="summary">Using EphB2 or the ISC marker Lgr5, we have FACS-purified and profiled intestinal stem cells (ISCs), crypt proliferative progenitors and late transient amplifying cells to define a gene expression program specific for normal ISCs. A frequent complication in colorectal cancer (CRC) is regeneration of the tumor after therapy. The intestinal stem cell signature predicts disease relapse in CRC and identifies a stem cell-like population that displays robust tumor- initiating capacity in immunodeficient mice as well as long-term self-renewal potential. We FACS purified mouse intestinal crypt cells according to their EphB2 or Lgr5 contents. We used Affymetrix chips to hybridize 2 samples from EphB2 high, 2 samples from EphB2 medium and 2 samples from EphB2 low cells (one sample from each group in a first hybridization on February 2009 plus an additional sample from each group on March 2009). Additionally, we hybridized one sample from Lgr5-EGFP high and one sample from Lgr5-EGFP low cells, obtained from Lgr5-EGFP knock-in mice (Barker et al., 2007).</item><item key="source">http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-27605</item><item key="sample_source">http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-27605/samples/</item></data></biogps>
