Apoptosis-inducing activity of synthetic hydrocarbon-stapled peptides in H358 cancer cells expressing KRAS.

Lung cancers are the leading cause of cancer deaths worldwide and pose a grave threat to human life and health. Non-small cell lung cancer (NSCLC) is the most frequent malignancy occupying 80% of all lung cancer subtypes. Except for other mutations (., ) that are also vital for the occurrence, gene mutation is a significant driving force of NSCLC, with a prevalence of approximately 14% of all NSCLC patients. However, there are only a few therapeutic drugs targeting KRAS mutations currently. Here, we synthesized hydrocarbon-stapled peptide that was much shorter and more stable with modest KRAS binding affinity and the same anti-tumor effect based on the -helical peptide mimic SAH-SOS1. The stapled peptide effectively induced G2/M arrest and apoptosis, inhibiting cell growth in KRAS-mutated lung cancer cells disrupting the KRAS-mediated RAF/MEK/ERK signaling, which was verified from the perspective of genomics and proteomics. Peptide also exhibited strong anti-trypsin and anti-chymotrypsin abilities, as well as good plasma stability and human liver microsomal metabolic stability. Overall, peptide retains the equivalent anti-tumor activity of SAH-SOS1 but with improved stability and affinity, superior to SAH-SOS1. Our work offers a structural optimization approach of KRAS peptide inhibitors for cancer therapy.