Research Press Release | August 06, 2019
Two known gene mutations induce pathways that enhance pancreatic cancer’s ability to invade tissues and evade the immune system. Researchers report the molecular details of this process providing insights into druggable targets for immunotherapies.
Mutations in the genes KRAS and TP53 are closely linked to pancreatic ductal adenocarcinoma, by far the most common type of pancreatic cancer. Pancreatic cancers are often already malignant when diagnosed, making its five-year survival rate extremely low — less than ten percent. So, understanding how it evolves at the molecular level could help anti-cancer drug development.
Hisataka Sabe of Hokkaido University and colleagues in Japan conducted tests in human cancer cells and in mouse models of the disease to investigate the roles of KRAS and TP53 gene mutations in pancreatic ductal adenocarcinoma. The study was published in the journal Proceedings of the National Academy of Sciences (PNAS).
They found that mutations in KRAS increased the production of two proteins, called ARF6 and AMAP1, which they previously discovered constitute a signalling pathway involved in cancer cell invasion and malignancy.
Mutations in the gene TP53 were also found to facilitate ARF6 activation, in addition to causing a metabolic pathway, called the mevalonate pathway, to go into overdrive. This pathway is known for its role in enhancing the invasiveness of some cancers.
Further investigations of the ARF6-AMAP1 pathway found it was involved in promoting cell-surface expression of an immune checkpoint protein, called PD-L1, on cancer cells, in addition to enhancing its recycling within the cell. PD-L1 expression on cancer cells helps them hide from the immune system, avoiding attack. Mutated KRAS and TP53 genes, and over-activation of the mevalonate pathway, both played crucial roles in the eventual cell-surface expression and recycling of PD-L1.
“We found that two well-known driver mutations of pancreatic cancer can promote both invasion to other tissues and evasion of the immune system through promoting the ARF6 pathway. This means that malignancies can develop in parallel with oncogenesis, making it difficult to detect cancer cells in its early stage,” says Hisataka Sabe. “Further studies are still needed to determine the extent of PD-L1 involvement in immune evasion. Studies are also needed to consider if PD-L1- and ARF6-targeting drugs can make pancreatic cancer cells more susceptible to attack by the immune system,” he continued.
Hashimoto S. et al., ARF6 and AMAP1 are major targets of KRAS and TP53 mutations to promote invasion, PD-L1 dynamics, and immune evasion of pancreatic cancer. Proceedings of the National Academy of Sciences (PNAS), August 5, 2019.
This study was supported by Grants-in-Aid from the Ministry of Education, Science, Sports and Culture (MEXT) of Japan, grants from the Takeda Science Foundation, the Mitsubishi Foundation, the Uehara Memorial Foundation, and the Suzuken Memorial Foundation, and a grant for basic science research projects from The Sumitomo Foundation, the Sumitomo Electronic Group Foundation, the Suhara Foundation, and the Ono Cancer Research Fund.
Professor Hisataka Sabe
Graduate School of Medicine
Naoki Namba (Media Officer)
Institute for International Collaboration