Variation in cancer-causing KRAS mutations greater than thought

The findings were published in PLOS Computational Biology.

Mutations occurring in the proteins of the human body often constitute a critical factor that predisposes to cancer development. In this sense, one of the most important proteins is KRAS, whose mutations play a role in the development of pancreatic cancer, among others. Point mutation of the glycine 12 amino acid of the KRAS protein can -- depending on the mutation -- cause glycine to mutate into any of the six possible different amino acids, all of which make the protein overactive. This causes uncontrolled cell growth and, consequently, the development of cancerous tissue.

Previously, all of the six different mutations occurring in the same location of the KRAS protein were regarded equal in their function. However, this may not be the case, as the newly published study now shows that these mutations are not fully random: different mutations occur more or less frequently in different tissue types. This suggests that different mutations may have a different effect on protein function.

The researchers conducted a thorough analysis of the effects of different mutations on protein function with the help of computer-simulated molecular dynamics. The simulation showed that different mutations have different effects on protein dynamics and, consequently, on protein function. These observed differences may partially explain why different mutations occur more or less frequently in different tissue types.

The study is the first to show that different mutations occurring in the same location have a different effect on the molecular-level function of the KRAS protein.

Mutations of the glycine 12 amino acid of the KRAS protein are most frequently discovered in cancer tumours of the colon, lungs and pancreas, and they are especially common in pancreatic ductal adenocarcinoma. Among the common cancers, pancreatic ductal adenocarcinoma is associated with the worst prognosis, with no effective treatment alternatives available. The findings enhance our understanding of the effects of different mutations. In the future, they may help in the development and selection of drug therapy alternatives targeting the function of the mutated KRAS protein.