<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>77(2)</volume><submitter>Shen M</submitter><pubmed_abstract>This study was to investigate the impact of exosomes-derived circ_0008039 on ferroptosis and stemness in colorectal cancer cells, as well as its associated molecular mechanisms. The cell colony formation ability was evaluated using the MTT assay and colony formation assay, respectively. Additionally, the sphere formation assay was employed to examine the cells' ability to aggregate into spheres. The targeting relationship between circ_0008039, miR-302e, and SLC7A11 was verified through dual luciferase assay. Furthermore, RNA immunoprecipitation (RIP) analysis of circ_0008039 and miR-302e was conducted. Western blotting was utilized to detect the protein expression of exosome surface antigens (TSG101 and CD63), stem cell markers (CD133, Nanog, and SOX-2), as well as SLC7A11 in both exosomes</pubmed_abstract><journal>Journal of clinical biochemistry and nutrition</journal><pagination>120-130</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12440672</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Tumor-derived exosomes containing circ_0008039 promote the stemness of colorectal cancer cells by inhibiting ferroptosis.</pubmed_title><pmcid>PMC12440672</pmcid><pubmed_authors>Shen M</pubmed_authors><pubmed_authors>Wan S</pubmed_authors><pubmed_authors>Yang X</pubmed_authors><pubmed_authors>Liu X</pubmed_authors><pubmed_authors>Ma L</pubmed_authors><pubmed_authors>Liao X</pubmed_authors></additional><is_claimable>false</is_claimable><name>Tumor-derived exosomes containing circ_0008039 promote the stemness of colorectal cancer cells by inhibiting ferroptosis.</name><description>This study was to investigate the impact of exosomes-derived circ_0008039 on ferroptosis and stemness in colorectal cancer cells, as well as its associated molecular mechanisms. The cell colony formation ability was evaluated using the MTT assay and colony formation assay, respectively. Additionally, the sphere formation assay was employed to examine the cells' ability to aggregate into spheres. The targeting relationship between circ_0008039, miR-302e, and SLC7A11 was verified through dual luciferase assay. Furthermore, RNA immunoprecipitation (RIP) analysis of circ_0008039 and miR-302e was conducted. Western blotting was utilized to detect the protein expression of exosome surface antigens (TSG101 and CD63), stem cell markers (CD133, Nanog, and SOX-2), as well as SLC7A11 in both exosomes</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Sep</publication><modification>2026-04-08T19:51:51.55Z</modification><creation>2026-04-08T14:35:29.336Z</creation></dates><accession>S-EPMC12440672</accession><cross_references><pubmed>40963723</pubmed><doi>10.3164/jcbn.24-240</doi></cross_references></HashMap>