TY - JOUR
T1 - Comparative pathology of nerve sheath tumors in mouse models and humans
AU - Stemmer-Rachamimov, Anat O.
AU - Louis, David N.
AU - Nielsen, Gunnlaugur P.
AU - Antonescu, Cristina R.
AU - Borowsky, Alexander D.
AU - Bronson, Roderick T.
AU - Burns, Dennis K.
AU - Cervera, Pascale
AU - McLaughlin, Margaret E.
AU - Reifenberger, Guido
AU - Schmale, Michael C.
AU - MacCollin, Mia
AU - Chao, Richard C.
AU - Cichowski, Karen
AU - Kalamarides, Michel
AU - Messerli, Shanta M.
AU - McClatchey, Andrea I.
AU - Niwa-Kawakita, Michiko
AU - Ratner, Nancy
AU - Reilly, Karlyne M.
AU - Zhu, Yuan
AU - Giovannini, Marco
PY - 2004/5/15
Y1 - 2004/5/15
N2 - Despite the progress made in our understanding of the biology of neurofibromatosis (NF), the long-term clinical outcome for affected patients has not changed significantly in the past decades, and both NF1 and NF2 are still associated with a significant morbidity and a decreased life span. A number of NF1 and NF2 murine models have been generated to aid in the study of NF tumor biology and in the development of targeted therapies for NF patients. A single, universal pathological classification of the lesions generated in these murine models is essential for the validation of the models, for their analysis and comparison with other models, and for their future effective use in preclinical treatment trials. For the formulation of a pathological classification of these lesions, the WHO classification of human tumors was used as a reference. However, it was not adopted for the classification of the GEM lesions because of some important differences between the human and murine lesions. A novel classification scheme for peripheral nerve sheath tumors in murine models was therefore devised.
AB - Despite the progress made in our understanding of the biology of neurofibromatosis (NF), the long-term clinical outcome for affected patients has not changed significantly in the past decades, and both NF1 and NF2 are still associated with a significant morbidity and a decreased life span. A number of NF1 and NF2 murine models have been generated to aid in the study of NF tumor biology and in the development of targeted therapies for NF patients. A single, universal pathological classification of the lesions generated in these murine models is essential for the validation of the models, for their analysis and comparison with other models, and for their future effective use in preclinical treatment trials. For the formulation of a pathological classification of these lesions, the WHO classification of human tumors was used as a reference. However, it was not adopted for the classification of the GEM lesions because of some important differences between the human and murine lesions. A novel classification scheme for peripheral nerve sheath tumors in murine models was therefore devised.
UR - http://www.scopus.com/inward/record.url?scp=2442681924&partnerID=8YFLogxK
U2 - 10.1158/0008-5472.CAN-03-4079
DO - 10.1158/0008-5472.CAN-03-4079
M3 - Article
C2 - 15150133
AN - SCOPUS:2442681924
SN - 0008-5472
VL - 64
SP - 3718
EP - 3724
JO - Cancer Research
JF - Cancer Research
IS - 10
ER -