Combination therapy targeting KRAS mutation could provide benefit to nearly a third of lung cancer patients, reveals a new study. The findings of the study are published in the journal Cancer Research.
Lung cancer is the second most common cancer found in both men and women. It is estimated there will be roughly 228,000 new lung cancer cases this year, and nearly 30% of those patients will have mutations in the KRAS pathway. This type of mutation makes cancer more aggressive and difficult to treat. Researchers at Moffitt Cancer Center are hoping to change that. In a new study the team discovered a new treatment approach that may help this group of patients.
KRAS is a gene that regulates cell signaling in an "on" and "off" manner, leading to normal cell growth and division. Mutations that occur in the KRAS gene cause the protein to ignore any "off" signals that it receives, which results in unchecked cell growth. This is why researchers have been investigating areas in the KRAS pathway as possible therapeutic targets. For example, in melanoma, therapies that target the BRAF mutation, a protein in the KRAS pathway, have led to positive patient response.
In this study, the research team found that MEK inhibitors increase the number of receptors on the cell surface for TNFα to bind to, which leads to the delivery of a more potent and sustained cell death signal. IFNγ, a cytokine known to be crucial for anti-tumor immunity, further enhances the anti-tumor activity of MEK inhibitors and TNFα. Importantly, MEK inhibitors also considerably increase expression of TNFα and IFNγ target genes, which can lead to increase in anti-tumor immunity.
"MEK inhibitors alone do not provide a strong overall response for this group of patients," said Amer A. Beg, Ph.D., a senior member of the Immunology Department and Lung Cancer Center of Excellence at Moffitt and lead author of this study. Beg, and his team took their research further by investigating whether MEK inhibitors in combination with therapies known to increase expression of TNFα and IFNγ would provide a better response. They discovered that adding a PD-1 immune checkpoint inhibitor with MEK inhibitors resulted in the strongest tumor regression in mice.
The researchers are planning further studies to combine MEK inhibitors with other immune therapies that provide a strong expression of these cytokines in the tumor microenvironment, such as CAR T and adoptive T cell therapy approaches.
"These studies will help determine if modulation of the immune microenvironment along with tumor signaling is a viable treatment strategy for lung cancer patients with KRAS mutations and potentially other mutations that rely on MEK signaling," said Mengyu Xie, a cancer biology graduate student studying at Moffitt and a first author of the study.
"Demonstrating that an anti-cancer agent can so effectively modulate the activity of a cytokine signaling pathway crucial for so many biological processes is conceptually novel and can lead to a new understanding of oncogenic pathways and strategies for targeting them," said Beg.