Rd. Cardiff et al., The mammary pathology of genetically engineered mice: the consensus reportand recommendations from the Annapolis meeting, ONCOGENE, 19(8), 2000, pp. 968-988
NIH sponsored a meeting of medical and veterinary pathologists with mammary
gland expertise in Annapolis in March 1999, Rapid development of mouse mam
mary models has accentuated the need for definitions of the mammary lesions
in genetically engineered mice (GEM) and to assess their usefulness as mod
els of human breast disease. The panel of nine pathologists independently r
eviewed material representing over 90% of the published systems, The GEM tu
mors were found to have: (1) phenotypes similar to those of non-GEM; (2) si
gnature phenotypes specific to the transgene; and (3) some morphological si
milarities to the human disease. The current mouse mammary and human breast
tumor classifications describe the majority of GEM lesions but unique morp
hologic lesions are found in many GEM. Since little information is availabl
e on the natural history of GEM lesions, a simple morphologic nomenclature
is proposed that allows direct comparisons between models. Future progress
requires rigorous application of guidelines covering pathologic examination
of the mammary gland and the whole animal. Since the phenotype of the lesi
ons is an essential component of their molecular pathology, funding agencie
s should adopt policies ensuring careful morphological evaluation of any fu
nded research involving animal models. A pathologist should be part of each
research team.