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The mammary pathology of genetically engineered mice: the consensus report and recommendations from the Annapolis meeting

  1. Author:
    Cardiff, R. D.
    Anver, M. R.
    Gusterson, B. A.
    Hennighausen, L.
    Jensen, R. A.
    Merino, M. J.
    Rehm, S.
    Russo, J.
    Tavassoli, F. A.
    Wakefield, L. M.
    Ward, J. M.
    Green, J. E.
  2. Author Address

    Cardiff RD Univ Calif Davis, UCD Ctr Comparat Med Cty Rd 98 & Hutchison Dr Davis, CA 95616 USA Univ Calif Davis, UCD Ctr Comparat Med Davis, CA 95616 USA NCI, Pathol Histotechnol Lab, SAIC Frederick, FCRDC Frederick, MD 21702 USA Inst Canc Res, Breakthrough toby Robins Breast Canc Res Ctr London SW3 6JB England NIDDK, Lab Genet & Physiol, NIH Bethesda, MD 20892 USA Vanderbilt Univ, Med Ctr, Dept Pathol Nashville, TN 37232 USA NCI, Pathol Lab, NIH Bethesda, MD 20892 USA Fox Chase Canc Ctr, Breast Canc Res Lab Philadelphia, PA 19111 USA SmithKline Beecham Pharmaceut King Of Prussia, PA 19406 USA Armed Forces Inst Pathol, Dept Gynecol & Breast Pathol Washington, DC 20306 USA NCI, Lab Cell Regulat & Carcinogenesis, NIH Bethesda, MD 20892 USA NCI, Vet & Tumor Pathol Sect, Off Lab Anim Resources Frederick, MD 21702 USA
    1. Year: 2000
  1. Journal: Oncogene
    1. 19
    2. 8 Special Issue SI
    3. Pages: 968-988
  2. Type of Article: Article
  1. Abstract:

    NIH sponsored a meeting of medical and veterinary pathologists with mammary gland expertise in Annapolis in March 1999, Rapid development of mouse mammary models has accentuated the need for definitions of the mammary lesions in genetically engineered mice (GEM) and to assess their usefulness as models of human breast disease. The panel of nine pathologists independently reviewed material representing over 90% of the published systems, The GEM tumors were found to have: (1) phenotypes similar to those of non-GEM; (2) signature phenotypes specific to the transgene; and (3) some morphological similarities to the human disease. The current mouse mammary and human breast tumor classifications describe the majority of GEM lesions but unique morphologic lesions are found in many GEM. Since little information is available 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 lesions is an essential component of their molecular pathology, funding agencies should adopt policies ensuring careful morphological evaluation of any funded research involving animal models. A pathologist should be part of each research team. [References: 68]

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