<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>8(1)</volume><submitter>Allen H</submitter><pubmed_abstract>Culturing 3D-expanded human placental-derived adherent stromal cells (ASCs) in the presence of tumor necrosis factor-alpha (TNF-α) and interferon-gamma (IFN-γ) transiently upregulated the secretion of numerous anti-proliferative, anti-angiogenic and pro-inflammatory cytokines. In a 3D-spheroid screening assay, conditioned medium from these induced-ASCs inhibited proliferation of cancer cell lines, including triple-negative breast cancer (TNBC) lines. In vitro co-culture studies of induced-ASCs with MDA-MB-231 human breast carcinoma cells, a model representing TNBC, supports a mechanism involving immunomodulation and angiogenesis inhibition. In vivo studies in nude mice showed that intramuscular administration of induced-ASCs halted MDA-MB-231 cell proliferation, and inhibited tumor progres</pubmed_abstract><journal>Scientific reports</journal><pagination>670</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5766494</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Human Placental-Derived Adherent Stromal Cells Co-Induced with TNF-α and IFN-γ Inhibit Triple-Negative Breast Cancer in Nude Mouse Xenograft Models.</pubmed_title><pmcid>PMC5766494</pmcid><pubmed_authors>Allen H</pubmed_authors><pubmed_authors>Aberman Z</pubmed_authors><pubmed_authors>Dego-Ashto T</pubmed_authors><pubmed_authors>Shraga-Heled N</pubmed_authors><pubmed_authors>Fuchs-Telem D</pubmed_authors><pubmed_authors>Blumenfeld M</pubmed_authors><pubmed_authors>Gilert A</pubmed_authors><pubmed_authors>Ofir R</pubmed_authors></additional><is_claimable>false</is_claimable><name>Human Placental-Derived Adherent Stromal Cells Co-Induced with TNF-α and IFN-γ Inhibit Triple-Negative Breast Cancer in Nude Mouse Xenograft Models.</name><description>Culturing 3D-expanded human placental-derived adherent stromal cells (ASCs) in the presence of tumor necrosis factor-alpha (TNF-α) and interferon-gamma (IFN-γ) transiently upregulated the secretion of numerous anti-proliferative, anti-angiogenic and pro-inflammatory cytokines. In a 3D-spheroid screening assay, conditioned medium from these induced-ASCs inhibited proliferation of cancer cell lines, including triple-negative breast cancer (TNBC) lines. In vitro co-culture studies of induced-ASCs with MDA-MB-231 human breast carcinoma cells, a model representing TNBC, supports a mechanism involving immunomodulation and angiogenesis inhibition. In vivo studies in nude mice showed that intramuscular administration of induced-ASCs halted MDA-MB-231 cell proliferation, and inhibited tumor progres</description><dates><release>2018-01-01T00:00:00Z</release><publication>2018 Jan</publication><modification>2025-04-21T16:16:36.173Z</modification><creation>2019-03-27T00:14:56Z</creation></dates><accession>S-EPMC5766494</accession><cross_references><pubmed>29330447</pubmed><doi>10.1038/s41598-017-18428-1</doi></cross_references></HashMap>