A fusion gene – formed by two separate parental genes through abnormal chromosomal rearrangement – may provide a clue and a marker for identifying a subgroup of the most common form of ovarian cancer, said researchers from Baylor College of Medicine in a report that appears in the Proceedings of the National Academy of Sciences.
“We identified a cancer-specific fusion gene between BCAM, a membrane adhesion molecule, and AKT2, a key kinase of a signaling pathway known to involve in tumor progression in high-grade serous ovarian cancer (the most common subtype of the disease), said Dr. Laising Yen, assistant professor of pathology & immunology at Baylor and corresponding author of the report.
The fusion gene produces a ‘chimeric’ fusion protein that is constantly activated, acting as a special kind of enzyme called a kinase, said Yen. When the fusion of the two genes is achieved by engineered chromosomal rearrangement using cultured cells, the cells become cancerous.
“While other fusion genes are present in high-grade serous ovarian carcinoma, the BCAM-AKT2 fusion gene is the most clinically relevant and functionally significant,” said Yen.
“This fusion gene could represent a marker for developing a better screening tool to identify a clinically relevant subtype among patients with this kind of cancer,” said Yen. “Furthermore, the aberrant fusion protein derived from the fusion gene could provide insight into the underlying mechanism of this deadly disease and serve as a drug target for future therapies.