<HashMap><database>biostudies-other</database><scores/><additional><omics_type>Unknown</omics_type><submitter>Wobus Manja</submitter><species>Homo sapiens</species><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-ECPF-GEOD-49858</full_dataset_link><project>EurocanPlatform</project><abstract>Disseminated tumor cells (DTCs) in the bone marrow can be detected in patients with solid tumors early on in disease progression. Via interaction with mesenchymal stromal cells (MSCs) these tumor cells may interfere with hematopoiesis. Using appropriate co-culture models, we investigated whether DTCs can change the bone marrow microenvironment by modulating MSC function with a special emphasis on their chemoattractive activity towards hematopoietic stem and progenitor cells (HSPCs). Human bone marrow derived MSCs as well as an immortalised MSC line (SCP-1) were co-cultured with MCF-7, MDA-MB231 breast carcinoma or MCF-10A non-malignant breast epithelial cells or their conditioned medium. Gene expression analysis of SCP-1 cells cultured with MCF-7 conditioned medium revealed SDF-1/CXCL12 as</abstract><repository>biostudies-other</repository><experiment_type>transcription profiling by array</experiment_type><data_source>EurocanPlatform</data_source><pubmed_authors>Wobus Manja</pubmed_authors><pubmed_authors>Bornhäuser Martin</pubmed_authors></additional><is_claimable>false</is_claimable><name>Gene expression of SCP-1 cells after incubation with conditioned medium of the breast carcinoma cell line MCF-7</name><description>Disseminated tumor cells (DTCs) in the bone marrow can be detected in patients with solid tumors early on in disease progression. Via interaction with mesenchymal stromal cells (MSCs) these tumor cells may interfere with hematopoiesis. Using appropriate co-culture models, we investigated whether DTCs can change the bone marrow microenvironment by modulating MSC function with a special emphasis on their chemoattractive activity towards hematopoietic stem and progenitor cells (HSPCs). Human bone marrow derived MSCs as well as an immortalised MSC line (SCP-1) were co-cultured with MCF-7, MDA-MB231 breast carcinoma or MCF-10A non-malignant breast epithelial cells or their conditioned medium. Gene expression analysis of SCP-1 cells cultured with MCF-7 conditioned medium revealed SDF-1/CXCL12 as</description><dates><release>2016-04-14T14:28:27Z</release><modification>2016-04-14T14:28:27Z</modification><creation>2016-04-14T14:28:27Z</creation></dates><accession>S-ECPF-GEOD-49858</accession><cross_references><GEO>GSE49858</GEO><ArrayExpress>E-GEOD-49858</ArrayExpress><EFO>EFO_0000305</EFO><EFO>EFO_0000322</EFO><ArrayExpress files>E-GEOD-49858</ArrayExpress files></cross_references></HashMap>