{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Sengupta R"],"funding":["NCATS NIH HHS","NICHD NIH HHS","NCI NIH HHS"],"pagination":["18282-92"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC4621891"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["6(21)"],"pubmed_abstract":["Tumor growth is not solely a consequence of autonomous tumor cell properties. Rather, tumor cells act upon and are acted upon by their microenvironment. It is tumor tissue biology that ultimately determines tumor growth. Thus, we developed a compound library screen for agents that could block essential tumor-promoting effects of the glioblastoma (GBM) perivascular stem cell niche (PVN). We modeled the PVN with three-dimensional primary cultures of human brain microvascular endothelial cells in Matrigel. We previously demonstrated stimulated growth of GBM cells in this PVN model and used this to assay PVN function. We screened the Microsource Spectrum Collection library for drugs that specifically blocked PVN function, without any direct effect on GBM cells themselves. Three candidate PVN-d"],"journal":["Oncotarget"],"pubmed_title":["Novel chemical library screen identifies naturally occurring plant products that specifically disrupt glioblastoma-endothelial cell interactions."],"pmcid":["PMC4621891"],"funding_grant_id":["P30 CA091842","R01 CA118389","T32 HD007499","UL1TR000448","P50 CA94056","P50 CA094056","UL1 TR000448"],"pubmed_authors":["Piwnica-Worms D","Rao S","Barone A","Marasa J","Taylor S","Jackson E","Leonard JR","Rubin JB","Warrington NM","Kim AH","Sengupta R"],"additional_accession":[]},"is_claimable":false,"name":"Novel chemical library screen identifies naturally occurring plant products that specifically disrupt glioblastoma-endothelial cell interactions.","description":"Tumor growth is not solely a consequence of autonomous tumor cell properties. Rather, tumor cells act upon and are acted upon by their microenvironment. It is tumor tissue biology that ultimately determines tumor growth. Thus, we developed a compound library screen for agents that could block essential tumor-promoting effects of the glioblastoma (GBM) perivascular stem cell niche (PVN). We modeled the PVN with three-dimensional primary cultures of human brain microvascular endothelial cells in Matrigel. We previously demonstrated stimulated growth of GBM cells in this PVN model and used this to assay PVN function. We screened the Microsource Spectrum Collection library for drugs that specifically blocked PVN function, without any direct effect on GBM cells themselves. Three candidate PVN-d","dates":{"release":"2015-01-01T00:00:00Z","publication":"2015 Jul","modification":"2025-04-06T19:45:35.841Z","creation":"2019-03-27T02:00:50Z"},"accession":"S-EPMC4621891","cross_references":{"pubmed":["26286961"],"doi":["10.18632/oncotarget.4957"]}}