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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="GSM610470"><item key="MALIGNANT POTENTIAL">non-malignant</item></item></item><item><item key="GSM610470"><item key="MALIGNANT POTENTIAL">non-malignant</item></item></item><item><item key="GSM610470"><item key="MALIGNANT POTENTIAL">non-malignant</item></item></item><item><item key="GSM610473"><item key="MALIGNANT POTENTIAL">intermediate</item></item></item><item><item key="GSM610473"><item key="MALIGNANT POTENTIAL">intermediate</item></item></item><item><item key="GSM610473"><item key="MALIGNANT POTENTIAL">intermediate</item></item></item><item><item key="GSM610476"><item key="MALIGNANT POTENTIAL">malignant</item></item></item><item><item key="GSM610476"><item key="MALIGNANT POTENTIAL">malignant</item></item></item><item><item key="GSM610476"><item key="MALIGNANT POTENTIAL">malignant</item></item></item></item><item key="id">6246</item><item key="pop_total">0</item><item key="platform">6</item><item key="summary_wrapped">Ovarian cancer is one of the most deadly cancers accounting for only 3% of diagnosed cancers, but is the fifth leading cause of cancer...</item><item key="geo_gse_id">E-GEOD-24789</item><item key="owner_profile">/profile/8773/arrayexpressuploader</item><item key="factor_count">1</item><item key="sample_count">9</item><item key="tags"><item>cancer</item><item>cell</item><item>intermediate</item><item>ovarian cancer</item><item>surface</item></item><item key="lastmodified">Dec.12, 2014</item><item key="is_default">False</item><item key="geo_gds_id"/><item key="slug">expression-data-from-mouse-ovarian-surface-epithel</item><item key="geo_id_plat">E-GEOD-24789_A-AFFY-45</item><item key="name">Expression data from mouse ovarian surface epithelium cells at different stages of malignancy</item><item key="created">Nov.11, 2014</item><item key="summary">Ovarian cancer is one of the most deadly cancers accounting for only 3% of diagnosed cancers, but is the fifth leading cause of cancer deaths among woman; however, the progression of ovarian cancer is poorly understood.  To study and further understand the early events that lead to epithelial derived ovarian cancer, we previously developed a cell model of progressive ovarian cancer. Mouse ovarian surface epithelial (MOSE) cells have undergone spontaneous transformation in cell culture and represent pre-neoplastic, non-tumorigenic to an aggressive malignant phenotype. Microarray analysis was performed with RNA isolated from different stages of MOSE cells to examine changes in gene expression as MOSE cells transition from a pre-neoplastic to a malignant state. RNA was isolated from MOSE early cell representing a pre-neoplastic, non-malignant stage, MOSE Intermediate cells representing a noeplastic, pre-invasive state, and MOSE Late cells representing a malignant, invasive stage.  Three biological replicates were used to take into account variations within the heterogeneous cultures.</item><item key="source">http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-24789</item><item key="sample_source">http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-24789/samples/</item></data></biogps>
