TAMPA, Fla. (Apr. 27, 2025) — A new study from researchers at shows that blocking a chemical process called nitrosylation could make one of the most aggressive forms of more treatable.
Their research, , focused on NRAS-mutant melanoma, a subtype that makes up about 25% of all melanoma cases. These cancers are difficult to treat and often resist current therapies, including immunotherapy and targeted drugs.
Researchers found that when nitrosylation is blocked, cancer cells become more sensitive to MEK inhibitors, a class of drugs that target the MEK-ERK pathway involved in tumor growth. The combination of nitrosylation inhibitors and MEK inhibitors led to slower tumor growth in lab experiments and animal models.
“Our research shows that nitrosylation helps cancer cells survive treatment and evade the immune system,” said , an assistant member in the at Moffitt and co-lead author on the study. “When we block it, we weaken the cancer’s defenses, kill the cancer cells and help the immune system attack the tumor.”
The study also found that blocking nitrosylation triggered immunogenic cell death, a process that causes tumor cells to release distress signals. These signals attracted immune cells such as CD8-positive T cells and dendritic cells, which can help destroy the cancer.
“This approach not only restrict the tumor growth but also enhances the body’s own anti-cancer immune response,” said Jyoti Srivastava, Ph.D., co-lead author and senior research scientist at Moffitt. “It could lead to more durable responses for patients who currently have limited options.”
The findings may offer a new path forward for patients with NRAS-mutant melanoma, which has few effective treatments. Researchers say the results support further study of nitrosylation inhibitors as part of combination therapy for melanoma and potentially other cancers.
This study was supported by pilot funds from Miles for Moffitt, Moffitt’s Molecular Medicine Program, the Donald A. Adam Melanoma and Skin Cancer Center of Excellence at Moffitt and the National Institutes of Health (R21ES035196).
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