<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Ribeiro DL</submitter><funding>Public Ministry of Labor Campinas (Research, Prevention and Education of Occupational Cancer)</funding><funding>São Paulo Research Foundation</funding><funding>FAPESP</funding><funding>State University of Londrina (UEL)</funding><funding>Coordination for the Improvement of Higher Education Personnel</funding><funding>Coordenação de Aperfeicoamento de Pessoal de Nível Superior</funding><funding>University of São Paulo (USP)</funding><funding>Maranhão Foundation for Research and Scientific and Technological Development</funding><funding>National Council for Scientific and Technological Development</funding><funding>Fundação de Amparo à Pesquisa e ao Desenvolvimento Científico e Tecnológico do Maranhão</funding><pagination>963</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9147598</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>14(5)</volume><pubmed_abstract>Metastatic prostate cancer (mPCa) is resistant to several chemotherapeutic agents. Brachydin A (BrA), a glycosylated flavonoid extracted from &lt;i>Fridericia platyphylla&lt;/i>, displays a remarkable antitumoral effect against in vitro mPCa cells cultured as bidimensional (2D) monolayers. Considering that three-dimensional (3D) cell cultures provide a more accurate response to chemotherapeutic agents, this study investigated the antiproliferative/antimetastatic effects of BrA and the molecular mechanisms underlying its action in mPCa spheroids (DU145) in vitro. BrA at 60-100 μM was cytotoxic, altered spheroid morphology/volume, and suppressed cell migration and tumor invasiveness. High-content analysis revealed that BrA (60-100 µM) reduced mitochondrial membrane potential and increased apoptosi</pubmed_abstract><journal>Pharmaceutics</journal><pubmed_title>The Antitumoral/Antimetastatic Action of the Flavonoid Brachydin A in Metastatic Prostate Tumor Spheroids In Vitro Is Mediated by (Parthanatos) PARP-Related Cell Death.</pubmed_title><pmcid>PMC9147598</pmcid><funding_grant_id># 00849/18</funding_grant_id><funding_grant_id>Research Productivity grant # 308231/2017</funding_grant_id><funding_grant_id># 2017/22305-9</funding_grant_id><funding_grant_id>National Postdoctoral Program PNPD grant # 88887.354023/2019 and Finance Code 001</funding_grant_id><funding_grant_id>Postdoctoral Fellowship grant #151520/2018-6 and Universal Project grant # 426246/2018-7</funding_grant_id><funding_grant_id>grant # 00849/18</funding_grant_id><funding_grant_id>Postdoctoral Fellowship grant #151520/2018-6</funding_grant_id><funding_grant_id>Universal Project grant # 426246/2018-7</funding_grant_id><pubmed_authors>Rocha CQD</pubmed_authors><pubmed_authors>Antunes LMG</pubmed_authors><pubmed_authors>Tuttis K</pubmed_authors><pubmed_authors>Oliveira LCB</pubmed_authors><pubmed_authors>Gomes INF</pubmed_authors><pubmed_authors>Lengert AVH</pubmed_authors><pubmed_authors>Serpeloni JM</pubmed_authors><pubmed_authors>Ribeiro DL</pubmed_authors><pubmed_authors>Reis RM</pubmed_authors><pubmed_authors>Colus IMS</pubmed_authors></additional><is_claimable>false</is_claimable><name>The Antitumoral/Antimetastatic Action of the Flavonoid Brachydin A in Metastatic Prostate Tumor Spheroids In Vitro Is Mediated by (Parthanatos) PARP-Related Cell Death.</name><description>Metastatic prostate cancer (mPCa) is resistant to several chemotherapeutic agents. Brachydin A (BrA), a glycosylated flavonoid extracted from &lt;i>Fridericia platyphylla&lt;/i>, displays a remarkable antitumoral effect against in vitro mPCa cells cultured as bidimensional (2D) monolayers. Considering that three-dimensional (3D) cell cultures provide a more accurate response to chemotherapeutic agents, this study investigated the antiproliferative/antimetastatic effects of BrA and the molecular mechanisms underlying its action in mPCa spheroids (DU145) in vitro. BrA at 60-100 μM was cytotoxic, altered spheroid morphology/volume, and suppressed cell migration and tumor invasiveness. High-content analysis revealed that BrA (60-100 µM) reduced mitochondrial membrane potential and increased apoptosi</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Apr</publication><modification>2026-06-21T03:16:37.653Z</modification><creation>2024-11-05T20:39:15.775Z</creation></dates><accession>S-EPMC9147598</accession><cross_references><pubmed>35631550</pubmed><doi>10.3390/pharmaceutics14050963</doi></cross_references></HashMap>