<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Chen YC</submitter><funding>Ministry of Science and Technology</funding><funding>National Sun Yat-sen University-KMU Joint Research Project</funding><funding>Kaohsiung Medical University Hospital</funding><funding>Kaohsiung Medical University Research Center</funding><pagination>641</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8870566</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>11(4)</volume><pubmed_abstract>Cryptocaryone (CPC) is a bioactive dihydrochalcone derived from &lt;i>Cryptocarya&lt;/i> plants, and its antiproliferation was rarely reported, especially for ovarian cancer (OVCA). This study aimed to examine the regulation ability and mechanism of CPC on three histotypes of OVCA cells (SKOV3, TOV-21G, and TOV-112D). In a 24 h MTS assay, CPC showed antiproliferation effects to OVCA cells, i.e., IC&lt;sub>50&lt;/sub> values 1.5, 3, and 9.5 μM for TOV-21G, SKOV3, and TOV-112D cells. TOV-21G and SKOV3 cells showed hypersensitivity to CPC when applied for exposure time and concentration experiments. For biological processes, CPC stimulated the generation of reactive oxygen species and mitochondrial superoxide and promoted mitochondrial membrane potential dysfunction in TOV-21G and SKOV3 cells. Apoptosis </pubmed_abstract><journal>Cells</journal><pubmed_title>Cryptocaryone Promotes ROS-Dependent Antiproliferation and Apoptosis in Ovarian Cancer Cells.</pubmed_title><pmcid>PMC8870566</pmcid><funding_grant_id>KMUH110-0R72</funding_grant_id><funding_grant_id>MOST 108-2314-B-037-021-MY3; MOST 108-2320-B-037-015-MY3; MOST 110-2314-B-037-075-MY2</funding_grant_id><funding_grant_id>KMU-TC108A04</funding_grant_id><funding_grant_id>#NSYSUKMU 111-P20</funding_grant_id><pubmed_authors>Chang HW</pubmed_authors><pubmed_authors>Chan TF</pubmed_authors><pubmed_authors>Yen CH</pubmed_authors><pubmed_authors>Chen YC</pubmed_authors><pubmed_authors>Chang HS</pubmed_authors><pubmed_authors>Yang CW</pubmed_authors><pubmed_authors>Farooqi AA</pubmed_authors><pubmed_authors>Huang MY</pubmed_authors></additional><is_claimable>false</is_claimable><name>Cryptocaryone Promotes ROS-Dependent Antiproliferation and Apoptosis in Ovarian Cancer Cells.</name><description>Cryptocaryone (CPC) is a bioactive dihydrochalcone derived from &lt;i>Cryptocarya&lt;/i> plants, and its antiproliferation was rarely reported, especially for ovarian cancer (OVCA). This study aimed to examine the regulation ability and mechanism of CPC on three histotypes of OVCA cells (SKOV3, TOV-21G, and TOV-112D). In a 24 h MTS assay, CPC showed antiproliferation effects to OVCA cells, i.e., IC&lt;sub>50&lt;/sub> values 1.5, 3, and 9.5 μM for TOV-21G, SKOV3, and TOV-112D cells. TOV-21G and SKOV3 cells showed hypersensitivity to CPC when applied for exposure time and concentration experiments. For biological processes, CPC stimulated the generation of reactive oxygen species and mitochondrial superoxide and promoted mitochondrial membrane potential dysfunction in TOV-21G and SKOV3 cells. Apoptosis </description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Feb</publication><modification>2025-04-26T19:02:30.91Z</modification><creation>2025-04-06T16:01:19.003Z</creation></dates><accession>S-EPMC8870566</accession><cross_references><pubmed>35203294</pubmed><doi>10.3390/cells11040641</doi></cross_references></HashMap>