Aime T. Franco1, Ronald A. Ghossein2,
H. Carl Le3, Jason A. Koutcher,4, Jame Fagin5
1Medicine & Human Human
Oncology & Pathogenesis Program, MSKCC, New York, NY, United States; 2Pathology,
MSKCC, New York, NY, United States; 3Medical Physics, MSKCC, New
York, NY, United States; 4Medicine, MSKCC; 5Medicine
& Human Oncology & Pathogenesis Program, MSKCC
We have developed mice with a thyroid-specific knock-in of oncogenic BRAF (LSL-BRAFV600E/TPO-Cre) to explore the role of pharmacological treatments in a physiologically relevant mouse model of PTC. Murine Braf-induced PTCs were treated with the specific allosteric MEK1/2 inhibitor PD325901 or rapamycin for three weeks, beginning at 3 weeks. We have used non-invasively measured thyroid volume by high resolution MRI as the tumor biomarker