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A mechanistically sound study combining genetic and pharmacological approaches in mouse and human models, demonstrating PRMT7 inhibition enhances CD8+ T cell function, but limited by single tumor model and lack of phase-controlled clinical trial.
Early-stage in vitro chemical screening with molecular modelling; no animal efficacy data, significant toxicity concerns (LD50 Category 2), and the authors themselves call for further optimization before preclinical development.
Mechanistic discovery study using cell assays, organoid and mouse models identifying Smyca-FOXM1 as a potential target, without clinical trial data or hard clinical outcomes to support therapeutic claims.