<HashMap><database>ENA</database><scores/><additional><omics_type>Genomics</omics_type><center_name>Massachusetts General Hospital, Harvard Medical School</center_name><full_dataset_link>https://www.ebi.ac.uk/ena/browser/view/PRJNA1014445</full_dataset_link><scientific_name>Homo sapiens</scientific_name><long_description>High-grade serous ovarian cancer (HGSC) is a challenging disease, especially for patients with immunologically 'cold' tumors devoid of tumor-infiltrating lymphocytes (TIL). HGSC exhibits among the highest levels of MYCN transcriptional signature in human cancer, which is strongly linked to diminished features of anti-tumor immunity. We used microarrays to identify genes potentially dysregulated by the oncogene N-MYC in HGSC cell lines. Overall design: CaOV3 TET-On MYCN-GFP and GFP control cells were cultured in the presence or absence of 1 ug/ml of Doxycycline (DOX) and collected for RNA extraction and hybridization on Clariom S microarrays.</long_description><repository>ENA</repository></additional><is_claimable>false</is_claimable><name>Expression data from CaOV3 TET-On cell line with MYCN inducible expression.</name><description>Expression data from CaOV3 TET-On cell line with MYCN inducible expression.</description><dates><last_updated>2025-09-24</last_updated><first_public>2023-12-09</first_public></dates><accession>PRJNA1014445</accession><cross_references><GEO>GSE242747</GEO><taxon>9606</taxon></cross_references></HashMap>