New insights into the roles of frequently mutated cancer genes have been provided in a comprehensive analysis of the genomes of nearly 500 papillary thyroid carcinomas (PTC), which is the most common form of thyroid cancer.
The findings also may help improve diagnosis and treatment. Investigators with The Cancer Genome Atlas (TCGA) Research Network identified new molecular subtypes that will help clinicians determine which tumors are more aggressive and which are more likely to respond to certain treatments.
AdvertisementTheir findings confirmed that PTCs are driven primarily by mutations in one of two cancer-associated genes: BRAF (and a particular mutation, V600E) or RAS. The work also detailed many differences between the two genetic types, particularly in signaling pathways that promote tumor development and growth. The researchers developed a scoring system to reflect gene expression in the two PTC types, allowing them to characterize tumors and determine both the pathway a tumor uses to send signals and its relative aggressiveness. Where a tumor lies on a scale - called its thyroid differentiation score - can have important treatment implications because different tumor signaling properties can mean the cancer responds differently to particular therapies.
The study also showed that BRAF-driven tumors have a broader range of genetic complexity than previously thought, with distinct subtypes. The results suggest a need for a new classification system that more accurately reflects underlying genetic characteristics of the cancer. The researchers, led by Thomas Giordano, M.D., Ph.D., University of Michigan, Ann Arbor, and Gad Getz, Ph.D., Broad Institute of MIT and Harvard, Cambridge, Massachusetts, reported their results online October 23, 2014, in Cell. Thyroid cancer is the fastest growing cancer in the United States, with more than 20,000 new PTC cases each year. Most thyroid cancers are slow-growing and treatable with surgery, hormone therapy and radioactive iodine. TCGA is a collaboration jointly supported and managed by the National Cancer Institute and the National Human Genome Research Institute, both parts of the National Institutes of Health.
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