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Publication : Multigenic and imprinting control of ovarian granulosa cell tumorigenesis in mice.

First Author  Beamer WG Year  1998
Journal  Cancer Res Volume  58
Issue  16 Pages  3694-9
PubMed ID  9721880 Mgi Jnum  J:49710
Mgi Id  MGI:1278042 Citation  Beamer WG, et al. (1998) Multigenic and imprinting control of ovarian granulosa cell tumorigenesis in mice. Cancer Res 58(16):3694-9
abstractText  Spontaneous juvenile ovarian granulosa cell (GC) tumors that occur in young girls are similar to GC carcinomas that develop in SWR-derived inbred mice. We analyzed female offspring from a series of matings among SWR and SJL inbred mice for chromosomal loci underlying tumor susceptibility. Intercross F-2 female mice were produced by reciprocal matings of (SWR x SJL)F-1 and (SJL x SWR)F-1 parents. Tumorigenesis in these: F-2 mice as well as in SWXJ recombinant inbred and congenic strains of mice derived from SWR and SJL showed significant (P < 0.001) association with Gct1, a dominant susceptibility locus on chromosome (CHR)4 and with Gct2 on CHR 12. Suggestive (P < 0.01) association was found with Gct3 on CHR 15. A fourth susceptibility locus, Gct4 on CHR X, was demonstrated with a strong parent-of-origin effect associated with the paternal genotype. Imprinting and complex interactions among these four loci combine to establish the probability for GC tumorigenesis in this mouse model.
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