<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>6</volume><submitter>Wang G</submitter><pubmed_abstract>The present study was (i) to prepare two types of selenium nanoparticles, namely an amorphous form of selenium quantum dots (A-SeQDs) and a crystalline form of selenium quantum dots (C-SeQDs); and (ii) to investigate the nano-bio interactions of A-SeQDs and C-SeQDs in MCF-7, HepG2, HeLa, NIH/3T3, L929 cells and BRL-3A cells. It was found that A-SeQDs could induce the mitochondria-mediated apoptosis, necrosis and death of cells, while C-SeQDs had much weaker effects. This polymorphs-dependent anti-proliferative activity of nano-selenium was scarcely reported. Further investigation demonstrated that A-SeQDs could differentially regulate 61 proteins and several pathways related to stress response, protein synthesis, cell migration and cell cycle, including "p38 MAPK Signaling", "p53 Signaling</pubmed_abstract><journal>Scientific reports</journal><pagination>31427</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4981849</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Mitochondria-Mediated Protein Regulation Mechanism of Polymorphs-Dependent Inhibition of Nanoselenium on Cancer Cells.</pubmed_title><pmcid>PMC4981849</pmcid><pubmed_authors>Yang G</pubmed_authors><pubmed_authors>Yang L</pubmed_authors><pubmed_authors>Guo Y</pubmed_authors><pubmed_authors>Zhu L</pubmed_authors><pubmed_authors>Zhang H</pubmed_authors><pubmed_authors>Ma X</pubmed_authors><pubmed_authors>Wang G</pubmed_authors><pubmed_authors>Wang X</pubmed_authors><pubmed_authors>Wang K</pubmed_authors><pubmed_authors>Sun J</pubmed_authors></additional><is_claimable>false</is_claimable><name>Mitochondria-Mediated Protein Regulation Mechanism of Polymorphs-Dependent Inhibition of Nanoselenium on Cancer Cells.</name><description>The present study was (i) to prepare two types of selenium nanoparticles, namely an amorphous form of selenium quantum dots (A-SeQDs) and a crystalline form of selenium quantum dots (C-SeQDs); and (ii) to investigate the nano-bio interactions of A-SeQDs and C-SeQDs in MCF-7, HepG2, HeLa, NIH/3T3, L929 cells and BRL-3A cells. It was found that A-SeQDs could induce the mitochondria-mediated apoptosis, necrosis and death of cells, while C-SeQDs had much weaker effects. This polymorphs-dependent anti-proliferative activity of nano-selenium was scarcely reported. Further investigation demonstrated that A-SeQDs could differentially regulate 61 proteins and several pathways related to stress response, protein synthesis, cell migration and cell cycle, including "p38 MAPK Signaling", "p53 Signaling</description><dates><release>2016-01-01T00:00:00Z</release><publication>2016 Aug</publication><modification>2026-05-01T00:07:54.404Z</modification><creation>2019-03-27T02:20:28Z</creation></dates><accession>S-EPMC4981849</accession><cross_references><pubmed>27514819</pubmed><doi>10.1038/srep31427</doi></cross_references></HashMap>