As　a　novel　form　of　regulated　cell　death,　ferroptosis　is　characterized　by　intracellular　iron　and　lipid　peroxide　accumulation,　which　is　different　from　other　regulated　cell　death　forms　morphologically,　biochemically,　and　immunologically.　Ferroptosis　is　regulated　by　iron　metabolism,　lipid　metabolism,　and　antioxidant　defense　systems　as　well　as　various　transcription　factors　and　related　signal　pathways.　Emerging　evidence　has　highlighted　that　ferroptosis　is　associated　with　many　physiological　and　pathological　processes,　including　cancer,　neurodegeneration　diseases,　cardiovascular　diseases,　and　ischemia/reperfusion　injury.　Noncoding　RNAs　are　a　group　of　functional　RNA　molecules　that　are　not　translated　into　proteins,　which　can　regulate　gene　expression　in　various　manners.　An　increasing　number　of　studies　have　shown　that　noncoding　RNAs,　especially　miRNAs,　lncRNAs,　and　circRNAs,　can　interfere　with　the　progression　of　ferroptosis　by　modulating　ferroptosis-related　genes　or　proteins　directly　or　indirectly.　In　this　review,　we　summarize　the　basic　mechanisms　and　regulations　of　ferroptosis　and　focus　on　the　recent　studies　on　the　mechanism　for　different　types　of　ncRNAs　to　regulate　ferroptosis　in　different　physiological　and　pathological　conditions,　which　will　deepen　our　understanding　of　ferroptosis　regulation　by　noncoding　RNAs　and　provide　new　insights　into　employing　noncoding　RNAs　in　ferroptosis-associated　therapeutic　strategies.