Enzyme Pair Identified as Target for Melanoma Chemotherapy

BET inhibitors are a class of drugs with anti-cancer, immunosuppressive, and other effects that are in clinical trials in the United States and Europe and are widely used in research. These molecules reversibly bind the bromodomains of bromodomain and extraterminal motif (BET) proteins BRD2, BRD3, BRD4, and BRDT, and prevent protein-protein interaction between BET proteins and acetylated histones and transcription factors.

Investigators at Mount Sinai School of Medicine (New York, NY, USA) reported in the November 16, 2017, issue of the journal Molecular Cell that they had identified AMIGO2 (Adhesion Molecule With Ig Like Domain 2), a transmembrane protein, as a BET target gene essential for melanoma cell survival. AMIGO2 was upregulated in melanoma cells and tissues compared to human melanocytes and nevi, and AMIGO2 silencing in melanoma cells induced G1/S arrest followed by apoptosis.

The investigators also reported that they had identified the pseudokinase PTK7 (Protein Tyrosine Kinase 7) as an AMIGO2 interactor whose function was regulated by AMIGO2. These results explained the mechanisms underlying the therapeutic effects of BETi in melanoma and suggested that the AMIGO2-PTK7 axis was a targetable pathway for treatment of metastatic melanoma.

"Melanoma is the most aggressive form of skin cancer, affecting more and more patients," said senior author, Dr. Emily Bernstein, associate professor of oncological sciences and dermatology at Mount Sinai School of Medicine. "While immunotherapy and targeted therapies have significantly improved the outcome for some metastatic melanoma patients, they have had success in a small subset of patients and can cause significant toxic side effects. Thus, their limitations underscore the need for new therapies, highlighting the importance of this research's discovery of novel targets."

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