Melanoma is a type of cancer originating from melanocytes, the cells responsible for producing skin pigment. It is known as the most lethal form of skin cancer due to its high rates of metastasis and recurrence. With the global trend of aging populations, the number of melanoma patients is rapidly increasing, and it is projected that by 2040, approximately 100,000 people worldwide will die from melanoma annually. In clinical practice, melanoma is currently treated with targeted therapies that inhibit the BRAF oncogene. However, drug resistance to BRAF inhibitors develops quickly, limiting the effectiveness of these treatments.

A research team led by Dr. Tackhoon Kim at the Center for Medicinal Materials Research at the Korea Institute of Science and Technology (KIST, President Sang-Rok Oh) has identified a new key mechanism behind the resistance of melanoma to BRAF inhibitors. It has proposed a strategy to develop new anticancer therapies to overcome this resistance.

The research team used melanoma cell line models resistant to BRAF inhibitors and discovered that the activation of the AMD1 gene plays a crucial role in the development of drug resistance. The AMD1 gene is essential for polyamine biosynthesis, which promotes cell growth and proliferation. It was found that polyamine levels are generally higher in BRAF inhibitor-resistant cancer cells. Through experiments, the team confirmed that inhibiting polyamine biosynthesis lowers resistance to BRAF inhibitors, leading to melanoma cell death.

Furthermore, the study revealed that the oncogene c-Myc triggers the increase of polyamine biosynthesis in BRAF-resistant melanoma. This increase in polyamines enhances mitochondrial protein levels, boosting mitochondrial activity and contributing to the proliferation of cancer cells resistant to treatment. The researchers identified this process as the core mechanism driving BRAF inhibitor resistance in melanoma. This is the first study in the world to pinpoint polyamine biosynthesis as a cause of BRAF inhibitor resistance. The KIST team also suggested an anticancer drug development strategy to block each stage of the resistance mechanism.

This research opens the door to developing new anticancer therapies based on regulating polyamine metabolism, which could be used to treat melanoma. This cancer has been difficult to cure due to frequent drug resistance. The team expects to secure leading technology applicable to the BRAF inhibitor market, projected to reach $1 billion by 2028.

Dr. Kim of KIST stated, "We have identified the key mechanism behind drug resistance in melanoma, the deadliest form of skin cancer. We plan to verify the anticancer effects of polyamine metabolism regulation in other cancers frequently associated with BRAF mutations, such as colorectal and thyroid cancers, as part of our drug development efforts."

(Newswise/VD)