Modeling Neurofibromatosis Type 1 Tumors in the Mouse for Therapeutic Intervention

Abstract

Von Recklinghausen's neurofibromatosis is a dominantly inherited cancer syndrome. Its gene encodes neurofibromin, a proteinwith ras GTPase-activating function (rasGAP) and, therefore, all NF1-associated pathology is thought to originate fromselective deregulation of the ras pathway. We have constructed a variety of mouse models for NF1 that permit recapitulationof the most common tumors seen in patients. In addition, these mouse models offer insights into tumor origin and intoparacrine interactions. Given the molecular and pathological fidelity of the mouse tumors to the human counterparts, it ishoped that these mouse strains will serve as effective tools for therapeutic discovery.