New! Sign up for our free email newsletter.
Science News
from research organizations

Possible new treatment strategy for lung cancer

Combination therapy targeting KRAS mutation could provide benefit to nearly a third of lung cancer patients

Date:
August 19, 2019
Source:
H. Lee Moffitt Cancer Center & Research Institute
Summary:
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 the cancer more aggressive and difficult to treat. Researchers are hoping to change that. They have now discovered a new treatment approach that may help this group of patients.
Share:
FULL STORY

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 the cancer more aggressive and difficult to treat. Researchers at Moffitt Cancer Center are hoping to change that. In a new study published in Cancer Research, 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 a positive patient response.

Moffitt researchers believe the MEK kinase, also found in the KRAS pathway, can be a possible target for lung cancer treatment. Through a series of drug screens, cell line and animal model experiments, they found that lung cancer cells treated with the MEK inhibitor trametinib in combination with the cytokines TNFα and IFNγ resulted in substantially more cell death than treating with a MEK inhibitor alone. TNFα was identified in the 1970s as Tumor Necrosis Factor but initial enthusiasm for using it in cancer treatment was quickly dampened by inflammatory response induced following TNFα administration, and the fact that most tumor cells resist killing by TNFα. 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 increases expression of TNFα and IFNγ target genes, which can lead to increase in anti-tumor immunity.

"MEK inhibitors alone do not provide strong overall response for this group of patients," said Amer A. Beg, Ph.D., 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 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 new understanding of oncogenic pathways and strategies for targeting them" said Beg.

This work was supported by funds from the Moffitt's Miles for Moffitt event and Lung Cancer Center of Excellence, Prelude to a Cure, and the Department of Defense Lung Cancer Research Program.


Story Source:

Materials provided by H. Lee Moffitt Cancer Center & Research Institute. Note: Content may be edited for style and length.


Journal Reference:

  1. Mengyu Xie, Hong Zheng, Ranjna Madan-Lala, Wenjie Dai, Nicholas T Gimbrone, Zhihua Chen, Fumi Kinose, Sarah A Blackstone, Keiran S.M. Smalley, W. Douglas Cress, Eric B Haura, Uwe Rix, Amer A Beg. MEK inhibition modulates cytokine response to mediate therapeutic efficacy in lung cancer. Cancer Research, 2019; canres.0698.2019 DOI: 10.1158/0008-5472.CAN-19-0698

Cite This Page:

H. Lee Moffitt Cancer Center & Research Institute. "Possible new treatment strategy for lung cancer." ScienceDaily. ScienceDaily, 19 August 2019. <www.sciencedaily.com/releases/2019/08/190819140213.htm>.
H. Lee Moffitt Cancer Center & Research Institute. (2019, August 19). Possible new treatment strategy for lung cancer. ScienceDaily. Retrieved February 26, 2024 from www.sciencedaily.com/releases/2019/08/190819140213.htm
H. Lee Moffitt Cancer Center & Research Institute. "Possible new treatment strategy for lung cancer." ScienceDaily. www.sciencedaily.com/releases/2019/08/190819140213.htm (accessed February 26, 2024).

Explore More
from ScienceDaily

RELATED STORIES