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Min mice provide a good model of human familial adenomatous polyposis. Recently, we have reported on two recombinant inbred lines (I and V) and the location of a modifier (Mom3) close to Apc, which altered polyp numbers in our mice possibly by modifying the frequency of wild-type (WT) allele loss at Apc; mice with severe disease (line V) showed elevated rates of loss. We now show that in line I only, a single pregnancy caused a significant increase in adenoma multiplicity compared with virgin controls (P<0.001) and that an additional pregnancy conferred a similar risk. Pregnancy was linked to both adenoma initiation and enhanced tumour growth in line I mice, and interline crosses indicated that susceptibility to pregnancy-associated adenomas was under genetic control. We found no evidence for the involvement of oestrodial metabolizing genes or the oestrogen receptors (Esr1 and 2) in tumour multiplicity. Importantly, a significantly elevated frequency of WT allele loss at Apc was observed in adenomas from parous mice (line and backcrossed) carrying the line I Min allele relative to equivalent virgin controls (P=0.015). Our results provide the first experimental evidence for genetic determinants controlling pregnancy-associated tumourigenesis; analogous genetic factors may exist in humans.

Original publication

DOI

10.1093/hmg/ddl419

Type

Journal article

Journal

Hum Mol Genet

Publication Date

01/12/2006

Volume

15

Pages

3429 - 3435

Keywords

Adenomatous Polyposis Coli, Animals, Chromosome Mapping, Disease Models, Animal, Female, Gene Frequency, Genes, APC, Genetic Markers, Genetic Predisposition to Disease, Humans, Mice, Mice, Mutant Strains, Pregnancy, Pregnancy Complications, Neoplastic, Receptors, Estrogen