Faculty Research 1990 - 1999

Title

Multiple mechanisms of tumorigenesis in E mu-myc transgenic mice.

Document Type

Article

Publication Date

1993

Keywords

Cell-Division, DNA: an, Female, Flow-Cytometry, Gene-Rearrangement, Genotype, Homozygote, Leukocytes: pa, tr, Lymphocytes: pa, Lymphoma-B-Cell: et, ge, pa, Male, Mice, Mice-Inbred-C57BL, Mice-Transgenic: ge, Neoplasm-Transplantation, Neoplasms: et, SUPPORT-U-S-GOVT-P-H-S

JAX Source

Cancer Res 1993 Apr 1;53(7):1665-9

Grant

CA35845/CA/NCI, AI20232/AI/NIAID, AI25765/AI/NIAID

Abstract

Transgenic mice bearing a c-myc oncogene under control of the immunoglobulin heavy chain enhancer (E mu-myc mice) reproducibly develop and die from tumors of the B lymphocyte lineage (J.M. Adams, A.W. Harris, C.A. Pinkert, L.M. Corcoran, W.S. Alexander, S. Cory, R.D. Palmiter, and R.L. Brinster, Nature (Lond.), 318: 533-538, 1985; W.Y. Langdon, A. W. Harris, S. Cory, and J.M. Adams, Cell 47: 11-18, 1986; A.W. Harris, C.A. Pinkert, M. Crawford, W.Y. Langdon, R.L. Brinster, and J.M. Adams, J. Exp. Med., 167: 353-371, 1988; reviewed in S. Cory and J.M. Adams, Annu. Rev. Immunol., 6: 25-48, 1988). Analysis of lymphocytes obtained by serial sampling of peripheral blood from individual hemizygous (E mu-myc/0) and homozygous (E mu-myc/E mu-myc) transgenic mice indicates that proliferation in the original host and transplantability into histocompatible recipients are distinct properties that can be acquired independently and in either order. These two types of transgenic mice differ in that homozygous mice have about one-fourth the life span of hemizygous mice and develop polyclonal, non-transplantable tumors in comparison to the oligoclonal, highly transplantable malignancies seen in hemizygous animals. In conclusion, the overall concept of malignancy is best viewed as an aggregate of the separable parameters of cellular proliferation, clonality, tissue invasiveness, metastasis, and (experimental) transplantability. The E mu-myc transgenic mouse represents an attractive model in which to investigate the multistep nature and alternative pathways of tumorigenesis.

Please contact the Joan Staats Library for information regarding this document.

Share

COinS