including nearly all triple-negative breast cancers (TNBCs). Because STAT3 is difficult to
target directly, we considered whether metabolic changes driven by activated STAT3 could
provide a therapeutic opportunity. We found that STAT3 prominently modulated several lipid
classes, with most profound effects on N-acyl taurine and arachidonic acid, both of which are
involved in plasma membrane remodeling. To exploit these metabolic changes …