ARE-PROTACs Enable Co-degradation of an Nrf2-MafG Heterodimer

Proteolysis-targeting chimera (PROTAC) technology has emerged as a potential strategy to degrade undruggable proteins in recent years. Nrf2, an aberrantly activated transcription factor in cancer, is generally considered undruggable as lacking active sites or allosteric pockets. Here, we constructed the chimeric molecule C2, which consists of an Nrf2-binding element and a CRBN ligand, as a first-in-class Nrf2 degrader. Surprisingly, C2 was found to selectively degrade an Nrf2-MafG heterodimer simultaneously via the ubiquitin-proteasome system. C2 impeded Nrf2-ARE transcrip-tional activity significantly and improved the sensitivity of NSCLC cells to ferroptosis and therapeutic drugs. The degradation character of ARE-PROTACs suggests that the PROTAC hijacking the transcription element of TFs could achieve co-degradation of the transcription complex.

Automated summary

PROTAC technology is a potential strategy to degrade undruggable proteins. By constructing a new Nrf2 degrader called C2, the Nrf2-MafG heterodimer was selectively degraded, leading to the inhibition of Nrf2 transcriptional activity and improved sensitivity of NSCLC cells to ferroptosis and therapeutic drugs.