<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Sogawa C</submitter><funding>Suzuken Memorial Foundation</funding><funding>Ryobi Teien Memory Foundation</funding><funding>Japan Society for the Promotion of Science</funding><pagination>E523</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7072357</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>12(2)</volume><pubmed_abstract>Tumor growth, progression, and therapy resistance are crucial factors in the prognosis of cancer. The properties of three-dimensional (3D) tumor-like organoids (tumoroids) more closely resemble in vivo tumors compared to two-dimensionally cultured cells and are therefore effectively used for assays and drug screening. We here established a repurposed drug for novel anticancer research and therapeutics using a 3D tumoroid-based screening system. We screened six pharmacologically active compounds by using an original tumoroid-based multiplex phenotypic screening system with a matrix metalloproteinase 9 (MMP9) promoter-driven fluorescence reporter for the evaluation of both tumoroid formation and progression. The antiparkinson drug benztropine was the most effective compound uncovered by the </pubmed_abstract><journal>Cancers</journal><pubmed_title>Antiparkinson Drug Benztropine Suppresses Tumor Growth, Circulating Tumor Cells, and Metastasis by Acting on SLC6A3/DAT and Reducing STAT3.</pubmed_title><pmcid>PMC7072357</pmcid><funding_grant_id>CS</funding_grant_id><funding_grant_id>TE</funding_grant_id><funding_grant_id>KO</funding_grant_id><funding_grant_id>17K11643</funding_grant_id><funding_grant_id>JP17K11642</funding_grant_id><funding_grant_id>JP17K11669</funding_grant_id><funding_grant_id>JP17K17895</funding_grant_id><funding_grant_id>JP17K11689</funding_grant_id><funding_grant_id>19H03817</funding_grant_id><funding_grant_id>19H04051</funding_grant_id><funding_grant_id>JP18K09789</funding_grant_id><pubmed_authors>Trin K</pubmed_authors><pubmed_authors>Tran MT</pubmed_authors><pubmed_authors>Taha EA</pubmed_authors><pubmed_authors>Ishige M</pubmed_authors><pubmed_authors>Sogawa C</pubmed_authors><pubmed_authors>Kawai H</pubmed_authors><pubmed_authors>Lu Y</pubmed_authors><pubmed_authors>Okamoto K</pubmed_authors><pubmed_authors>Sogawa N</pubmed_authors><pubmed_authors>Calderwood SK</pubmed_authors><pubmed_authors>Okusha Y</pubmed_authors><pubmed_authors>Kozaki KI</pubmed_authors><pubmed_authors>Eguchi T</pubmed_authors><pubmed_authors>Takigawa M</pubmed_authors></additional><is_claimable>false</is_claimable><name>Antiparkinson Drug Benztropine Suppresses Tumor Growth, Circulating Tumor Cells, and Metastasis by Acting on SLC6A3/DAT and Reducing STAT3.</name><description>Tumor growth, progression, and therapy resistance are crucial factors in the prognosis of cancer. The properties of three-dimensional (3D) tumor-like organoids (tumoroids) more closely resemble in vivo tumors compared to two-dimensionally cultured cells and are therefore effectively used for assays and drug screening. We here established a repurposed drug for novel anticancer research and therapeutics using a 3D tumoroid-based screening system. We screened six pharmacologically active compounds by using an original tumoroid-based multiplex phenotypic screening system with a matrix metalloproteinase 9 (MMP9) promoter-driven fluorescence reporter for the evaluation of both tumoroid formation and progression. The antiparkinson drug benztropine was the most effective compound uncovered by the </description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Feb</publication><modification>2025-04-26T01:06:20.327Z</modification><creation>2020-05-22T13:28:38Z</creation></dates><accession>S-EPMC7072357</accession><cross_references><pubmed>32102440</pubmed><doi>10.3390/cancers12020523</doi></cross_references></HashMap>