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Thyroid cancer is common, yet the sequence of alterations that promote tumor formation are incompletely understood. Here, we describe a novel model of thyroid carcinoma in zebrafish that reveals temporal changes due to BRAFV600E. Through the use of real-time in vivo imaging, we observe disruption in thyroid follicle structure that occurs early in thyroid development. Combinatorial treatment using BRAF and MEK inhibitors reversed the developmental effects induced by BRAFV600E. Adult zebrafish expressing BRAFV600E in thyrocytes developed invasive carcinoma. We identified a gene expression signature from zebrafish thyroid cancer that is predictive of disease-free survival in patients with papillary thyroid cancer. Gene expression studies nominated TWIST2 as a key effector downstream of BRAF. Using CRISPR/Cas9 to genetically inactivate a TWIST2 orthologue, we suppressed the effects of BRAFV600E and restored thyroid morphology and hormone synthesis. These data suggest that expression of TWIST2 plays a role in an early step of BRAFV600E-mediated transformation.

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EMT, cancer biology, epithelial cells, gene expression, human biology, medicine, protooncogenes, zebrafish, Animals, Disease Models, Animal, Gene Deletion, Gene Expression Profiling, Gene Expression Regulation, Morphogenesis, Mutant Proteins, Mutation, Missense, Proto-Oncogene Proteins B-raf, Thyroid Gland, Thyroid Hormones, Thyroid Neoplasms, Twist-Related Protein 2, Zebrafish