Background: RNA-binding proteins (RBPs) are critical players in oncogenesis and cancer progression, and hence promising drug targets. However, they are considered “undruggable” due to complex nature of RNA-protein interactions, lack of binding pockets and intrinsically disordered regions.
Aims: Accordingly, we have developed a conceptually new approach to drug these proteins by a rational modification of specific residues using innovative chemical probes.
Methods and Results: We initially adapted a site-selective protein modification approach (chemical editing) to identify functionally relevant and druggable cysteines in the oncofetal and pro-oncogenic IGF2 mRNA binding protein 1(IMP1). Subsequently, we tested the druggability of the identified residues by employing computational chemistry, cysteine-directed probes and cell-based chemical biology tools. Our efforts have uncovered residues C253 and C336, which were directly linked to IMP1 pro-oncogenic activity, and the discovery of J5 as a dual targeting covalent inhibitor. J5 impaired tumour growth and metastasis of ovarian cancer xenografts by the cysteine-specific modification of C253 and C336, which led to selective deregulation of IMP1-enhanced oncogene expression.
Conclusions: These results demonstrate the potential of our approach to discover and enable the rational modification of functionally relevant cysteines in RBPs as an innovative cancer therapy