<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Gross SM</submitter><funding>U.S. Department of Health &amp; Human Services | National Institutes of Health (NIH)</funding><pagination>1066</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9546880</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>5(1)</volume><pubmed_abstract>The phenotype of a cell and its underlying molecular state is strongly influenced by extracellular signals, including growth factors, hormones, and extracellular matrix proteins. While these signals are normally tightly controlled, their dysregulation leads to phenotypic and molecular states associated with diverse diseases. To develop a detailed understanding of the linkage between molecular and phenotypic changes, we generated a comprehensive dataset that catalogs the transcriptional, proteomic, epigenomic and phenotypic responses of MCF10A mammary epithelial cells after exposure to the ligands EGF, HGF, OSM, IFNG, TGFB and BMP2. Systematic assessment of the molecular and cellular phenotypes induced by these ligands comprise the LINCS Microenvironment (ME) perturbation dataset, which has</pubmed_abstract><journal>Communications biology</journal><pubmed_title>A multi-omic analysis of MCF10A cells provides a resource for integrative assessment of ligand-mediated molecular and phenotypic responses.</pubmed_title><pmcid>PMC9546880</pmcid><funding_grant_id>U54-HG008097</funding_grant_id><funding_grant_id>U54HL127366</funding_grant_id><funding_grant_id>U54HL127624</funding_grant_id><funding_grant_id>U54-HG008100</funding_grant_id><funding_grant_id>U54NS091046</funding_grant_id><pubmed_authors>Jaffe JD</pubmed_authors><pubmed_authors>Jacobson C</pubmed_authors><pubmed_authors>Lu X</pubmed_authors><pubmed_authors>Adam M</pubmed_authors><pubmed_authors>Lu Y</pubmed_authors><pubmed_authors>Mullahoo J</pubmed_authors><pubmed_authors>Wassie B</pubmed_authors><pubmed_authors>Subramanian A</pubmed_authors><pubmed_authors>Korkola JE</pubmed_authors><pubmed_authors>Evangelista JE</pubmed_authors><pubmed_authors>Clarke DJB</pubmed_authors><pubmed_authors>Pillai A</pubmed_authors><pubmed_authors>Subramanian K</pubmed_authors><pubmed_authors>McLean IC</pubmed_authors><pubmed_authors>Wang Y</pubmed_authors><pubmed_authors>Yapp C</pubmed_authors><pubmed_authors>Li J</pubmed_authors><pubmed_authors>Papanastasiou M</pubmed_authors><pubmed_authors>Xie Z</pubmed_authors><pubmed_authors>Fraenkel E</pubmed_authors><pubmed_authors>Heiser LM</pubmed_authors><pubmed_authors>Pessa S</pubmed_authors><pubmed_authors>Ma'ayan A</pubmed_authors><pubmed_authors>Bucher E</pubmed_authors><pubmed_authors>Lyons N</pubmed_authors><pubmed_authors>Vidovic D</pubmed_authors><pubmed_authors>Gross SM</pubmed_authors><pubmed_authors>Torre D</pubmed_authors><pubmed_authors>Derrick DS</pubmed_authors><pubmed_authors>Erdem C</pubmed_authors><pubmed_authors>Liu M</pubmed_authors><pubmed_authors>Sanchez-Aguila C</pubmed_authors><pubmed_authors>Dane MA</pubmed_authors><pubmed_authors>Daily K</pubmed_authors><pubmed_authors>Kilburn DF</pubmed_authors><pubmed_authors>Lee A</pubmed_authors><pubmed_authors>Feiler HS</pubmed_authors><pubmed_authors>Schurer S</pubmed_authors><pubmed_authors>London AB</pubmed_authors><pubmed_authors>Smith RL</pubmed_authors><pubmed_authors>Omberg L</pubmed_authors><pubmed_authors>Sorger PK</pubmed_authors><pubmed_authors>Natoli T</pubmed_authors><pubmed_authors>Chung M</pubmed_authors><pubmed_authors>Devlin KL</pubmed_authors><pubmed_authors>Mills CE</pubmed_authors><pubmed_authors>Liby TA</pubmed_authors><pubmed_authors>Gray JW</pubmed_authors><pubmed_authors>Birtwistle MR</pubmed_authors><pubmed_authors>Mills GB</pubmed_authors></additional><is_claimable>false</is_claimable><name>A multi-omic analysis of MCF10A cells provides a resource for integrative assessment of ligand-mediated molecular and phenotypic responses.</name><description>The phenotype of a cell and its underlying molecular state is strongly influenced by extracellular signals, including growth factors, hormones, and extracellular matrix proteins. While these signals are normally tightly controlled, their dysregulation leads to phenotypic and molecular states associated with diverse diseases. To develop a detailed understanding of the linkage between molecular and phenotypic changes, we generated a comprehensive dataset that catalogs the transcriptional, proteomic, epigenomic and phenotypic responses of MCF10A mammary epithelial cells after exposure to the ligands EGF, HGF, OSM, IFNG, TGFB and BMP2. Systematic assessment of the molecular and cellular phenotypes induced by these ligands comprise the LINCS Microenvironment (ME) perturbation dataset, which has</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Oct</publication><modification>2025-04-25T17:37:44.69Z</modification><creation>2024-11-08T20:52:11.089Z</creation></dates><accession>S-EPMC9546880</accession><cross_references><pubmed>36207580</pubmed><doi>10.1038/s42003-022-03975-9</doi></cross_references></HashMap>