PT  - JOURNAL ARTICLE
AU  - Jennifer L. Gorman
AU  - Jessica R. Adams
AU  - Emma M. Jones
AU  - Sean E. Egan
AU  - James R. Woodgett
TI  - Development of a drug repressible β-catenin mutant mouse to examine effect of activated β-catenin signaling on long-term maintenance of mammary tumor growth
AID  - 10.1101/588459
DP  - 2019 Jan 01
TA  - bioRxiv
PG  - 588459
4099  - http://biorxiv.org/content/early/2019/03/26/588459.short
4100  - http://biorxiv.org/content/early/2019/03/26/588459.full
AB  - Stabilized β-catenin expression is a well described initiator of mammary tumorigenesis in the mouse and elevated nuclear expression of this protein has been observed in human triple-negative tumor samples. However, the importance of stabilized β-catenin to continued tumor growth after initiation, and in the context of other driver mutations, has yet to be elucidated. To ascertain the importance of stabilized β-catenin after tumor initiation, we generated a novel transgenic mouse model, utilizing the tet-off system, to control expression of a stabilized mutant of β-catenin. Pups from early litters carrying one allele of regulatable stabilized β-catenin at the Rosa26 locus, but not targeted by Cre, were smaller in size compared with wildtype littermates and also developed skin lesions, requiring euthanasia. Maintenance of breeding cages on doxycycline chow allowed for healthy transgenic pups to survive past 3 weeks of age and 6 animal cohorts were established. We used two different mammary Cre strains, WAP-Cre and MMTV-NLST-Cre, crossed with regulatable, stabilized β-catenin (bcatFL) animals, as well as animals expressing mutated p53-R270H. While mammary tumors developed in animals expressing Cre-targeted regulatable bcatFL, the penetrance and growth kinetics were lower than observed with other mammary mouse models expressing stabilized β-catenin. Since fewer animals developed tumors, we focused analysis on the effect of turning off stabilized β-catenin expression following tumor initiation. In the animals examined, a delay in tumor growth, but not regression, was observed in animals expressing Cretargeted bcatFL as well as those expressing both bcatFL and p53-R270H. These results indicate that in a less aggressive β-catenin model, additional mutations likely provide independence from the initiating event.