<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Zani AP</submitter><funding>Financier of Studies and Projects</funding><funding>National Council for Scientific and Technological Development</funding><pagination>317</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9952489</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>12(2)</volume><pubmed_abstract>Cervical cancer is a health problem among women worldwide. Considering the limitations of prevention and antineoplastic chemotherapy against cervical cancer, research is needed to discover new, more effective, and safe antitumor agents. In the present study, we investigated the in vitro cytotoxicity of a new synthetic dibenzylideneacetone derived from 1,5-diaryl-3-oxo-1,4-pentadienyl (&lt;b>A3K2A3&lt;/b>) against cervical cancer cells immortalized by HPV 16 (SiHa), and 18 (HeLa) by MTT assay. Furthermore, we performed spectrofluorimetry, flow cytometry, and Western blot analyzes to explore the inhibitory mechanism of &lt;b>A3K2A3&lt;/b> in cervical cancer cells. &lt;b>A3K2A3&lt;/b> showed cytotoxic activity against both cell lines. Mitochondrial depolarization and reduction in intracellular ATP levels were </pubmed_abstract><journal>Antioxidants (Basel, Switzerland)</journal><pubmed_title>Dibenzylideneacetone Induces Apoptosis in Cervical Cancer Cells through Ros-Mediated Mitochondrial Damage.</pubmed_title><pmcid>PMC9952489</pmcid><funding_grant_id>421944/2018-8</funding_grant_id><pubmed_authors>Garcia FP</pubmed_authors><pubmed_authors>Din ZU</pubmed_authors><pubmed_authors>Nakamura CV</pubmed_authors><pubmed_authors>Zani AP</pubmed_authors><pubmed_authors>Rodrigues-Filho E</pubmed_authors><pubmed_authors>Zani CP</pubmed_authors><pubmed_authors>Ueda-Nakamura T</pubmed_authors><pubmed_authors>de Oliveira Silva S</pubmed_authors></additional><is_claimable>false</is_claimable><name>Dibenzylideneacetone Induces Apoptosis in Cervical Cancer Cells through Ros-Mediated Mitochondrial Damage.</name><description>Cervical cancer is a health problem among women worldwide. Considering the limitations of prevention and antineoplastic chemotherapy against cervical cancer, research is needed to discover new, more effective, and safe antitumor agents. In the present study, we investigated the in vitro cytotoxicity of a new synthetic dibenzylideneacetone derived from 1,5-diaryl-3-oxo-1,4-pentadienyl (&lt;b>A3K2A3&lt;/b>) against cervical cancer cells immortalized by HPV 16 (SiHa), and 18 (HeLa) by MTT assay. Furthermore, we performed spectrofluorimetry, flow cytometry, and Western blot analyzes to explore the inhibitory mechanism of &lt;b>A3K2A3&lt;/b> in cervical cancer cells. &lt;b>A3K2A3&lt;/b> showed cytotoxic activity against both cell lines. Mitochondrial depolarization and reduction in intracellular ATP levels were </description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Jan</publication><modification>2025-04-05T07:24:30.351Z</modification><creation>2025-04-05T07:24:30.351Z</creation></dates><accession>S-EPMC9952489</accession><cross_references><pubmed>36829876</pubmed><doi>10.3390/antiox12020317</doi></cross_references></HashMap>