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<biogps><data><item key="owner">ArrayExpress Uploader</item><item key="pop_total">0</item><item key="id">1572</item><item key="factors"><item><item key="GSE8096GSM200741"/></item><item><item key="GSE8096GSM200757"/></item><item><item key="GSE8096GSM200754"/></item><item><item key="GSE8096GSM200740"/></item><item><item key="GSE8096GSM200748"/></item><item><item key="GSE8096GSM200755"/></item><item><item key="GSE8096GSM200749"/></item><item><item key="GSE8096GSM200743"/></item><item><item key="GSE8096GSM200739"/></item><item><item key="GSE8096GSM200612"/></item><item><item key="GSE8096GSM200742"/></item><item><item key="GSE8096GSM200756"/></item></item><item key="ownerprofile_id">arrayexpress_sid</item><item key="platform">3</item><item key="summary_wrapped">Nonmalignant human mammary epithelial cells (HMEC) seeded in laminin-rich extracellular matrix (lrECM) form polarized acini and, in doing...</item><item key="pubmed_id">16849555</item><item key="geo_gse_id">E-GEOD-8096</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>breast</item><item>breast cancer</item><item>cancer</item><item>laminin</item></item><item key="lastmodified">Dec.12, 2014</item><item key="is_default">False</item><item key="geo_gds_id"/><item key="slug">transcription-profiling-of-human-mammary-epithelia</item><item key="geo_id_plat">E-GEOD-8096_A-AFFY-33</item><item key="name">Transcription profiling of human mammary epithelial cell lines with finite life span and immortal non-malignant cells - time series</item><item key="created">Jun.19, 2014</item><item key="summary">Nonmalignant human mammary epithelial cells (HMEC) seeded in laminin-rich extracellular matrix (lrECM) form polarized acini and, in doing so, transit from a disorganized proliferating state to an organized growth-arrested state. We hypothesized that the gene expression pattern of organized and growth-arrested HMECs would share similarities with breast tumors with good prognoses. Using Affymetrix HG-U133A microarrays, we analyzed the expression of 22,283 gene transcripts in 184 (finite life span) and HMT3522 S1 (immortal nonmalignant) HMECs on successive days after seeding in a lrECM assay. Both HMECs underwent growth arrest in G0-G1 and differentiated into polarized acini between days 5 and 7. We identified gene expression changes with the same temporal pattern in both lines and examined the expression of these genes in a previously published panel of microarray data for 295 breast cancer samples. We show that genes that are significantly lower in the organized, growth-arrested HMEC than in their proliferating counterparts can be used to classify breast cancer patients into poor and good prognosis groups with high accuracy. This study represents a novel unsupervised approach to identifying breast cancer markers that may be of use clinically. Experiment Overall Design: We analyzed gene expression in 184 (finite life span) and HMT3522 S1 (immortal non-malignant) HMECs on successive days (3, 5, and 7) post-seeding in a laminin-rich extracellular matrix assay. Both HMECs underwent growth arrest in G0/G1 and differentiated into polarized acini between days 5 and 7.</item><item key="source">http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-8096</item><item key="species">human</item><item key="sample_source">http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-8096/samples/</item></data></biogps>
