<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Cui J</submitter><funding>Swiss National Science Foundation</funding><pagination>1007-1022</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5352030</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>8(1)</volume><pubmed_abstract>Cancer stem cells (CSCs) play major roles in cancer initiation, metastasis, recurrence and therapeutic resistance. Targeting CSCs represents a promising strategy for cancer treatment. The purpose of this study was to identify selective inhibitors of breast CSCs (BCSCs). We carried out a cell-based phenotypic screening with cell viability as a primary endpoint, using a collection of 2,546 FDA-approved drugs and drug-like molecules in spheres formed by malignant human breast gland-derived cells (HMLER-shEcad cells, representing BCSCs) and control immortalized non-tumorigenic human mammary cells (HMLE cells, representing normal stem cells). 19 compounds were identified from screening. The chemically related molecules benztropine mesylate and deptropine citrate were selected for further valida</pubmed_abstract><journal>Oncotarget</journal><pubmed_title>New use of an old drug: inhibition of breast cancer stem cells by benztropine mesylate.</pubmed_title><pmcid>PMC5352030</pmcid><funding_grant_id>147087</funding_grant_id><pubmed_authors>Schneider G</pubmed_authors><pubmed_authors>Hollmen M</pubmed_authors><pubmed_authors>Proulx ST</pubmed_authors><pubmed_authors>Reker D</pubmed_authors><pubmed_authors>Cui J</pubmed_authors><pubmed_authors>Chen Y</pubmed_authors><pubmed_authors>Li L</pubmed_authors><pubmed_authors>Detmar M</pubmed_authors></additional><is_claimable>false</is_claimable><name>New use of an old drug: inhibition of breast cancer stem cells by benztropine mesylate.</name><description>Cancer stem cells (CSCs) play major roles in cancer initiation, metastasis, recurrence and therapeutic resistance. Targeting CSCs represents a promising strategy for cancer treatment. The purpose of this study was to identify selective inhibitors of breast CSCs (BCSCs). We carried out a cell-based phenotypic screening with cell viability as a primary endpoint, using a collection of 2,546 FDA-approved drugs and drug-like molecules in spheres formed by malignant human breast gland-derived cells (HMLER-shEcad cells, representing BCSCs) and control immortalized non-tumorigenic human mammary cells (HMLE cells, representing normal stem cells). 19 compounds were identified from screening. The chemically related molecules benztropine mesylate and deptropine citrate were selected for further valida</description><dates><release>2017-01-01T00:00:00Z</release><publication>2017 Jan</publication><modification>2025-04-04T09:00:55.085Z</modification><creation>2019-03-27T02:38:41Z</creation></dates><accession>S-EPMC5352030</accession><cross_references><pubmed>27894093</pubmed><doi>10.18632/oncotarget.13537</doi></cross_references></HashMap>