Ontology highlight
ABSTRACT: Background
Emerging evidence suggests that ferroptosis resistance may drives colorectal cancer (CRC) pathogenesis and limits therapeutic efficacy. A previous study has reported that lactate can enhance ferroptosis in CRC cells. The objective of this study was to elucidate how lactate regulates ferroptosis in CRC and to identify potential therapeutic targets.Methods
Cellular viability and proliferative capacities were determined via cell counting kit-8 (CCK-8) and colony formation. Ferroptosis-related and inflammatory markers, including malondialdehyde (MDA), Fe2+, glutathione (GSH), IL-1β, IL-12 and IL-10, were quantified by commercial kits. Protein and RNA interactions were investigated using co-immunoprecipitation (Co-IP), RNA pull-down, dual-luciferases report
SUBMITTER: Zhu JF
PROVIDER: S-EPMC12706171 | biostudies-literature | 2025 Dec
REPOSITORIES: biostudies-literature