Researchers identify new approach to overcome resistance to KRAS-targeted therapies

Many cancers with KRAS mutations, the most commonly mutated oncogene, develop rapid resistance to targeted therapy with KRAS inhibitors. A recent study by , , and , and colleagues discovered that SDC1, a cell surface protein involved downstream of the KRAS-mutated pathway and associated with pancreatic cancer progression, plays a critical role in acquired resistance to KRAS inhibitors. In preclinical models of KRAS-mutant pancreatic and colorectal cancers, SDC1 expression on the cell surface initially declined following KRAS inhibition but later re-emerged in resistant tumors. Mechanistic analyses uncovered the YAP1 oncogene as a major coordinator of SDC1 cell surface reactivation that further mediates the activation of multiple receptor tyrosine kinases and drives the development of KRAS inhibitor resistance. These findings highlight the YAP1-SDC1 axis as a key mechanism underlying this resistance and point to promising potential therapeutic vulnerability to enhance the durability of KRAS-targeted therapies. Further, the researchers suggest SDC1 may be a useful biomarker for monitoring relapse following KRAS inhibitor treatment. Learn more in  

These SDC1 findings are important discoveries as they hold potential for both therapeutic strategies and as predictive biomarkers.

Wantong Yao, M.D., Ph.D.

Translational Molecular Pathology