Table 1.
Purpose | Genotype | No. mice | No. mice that developed mammary tumor | Tumor incidence (%) |
---|---|---|---|---|
Expt. | H+/- T+/- R+/-, Dox(+) | 16 | 9* | 56 |
Control | H+/- T+/- R+/-, Dox(-) | 18 | 18 | 100 |
Control | H+/- T-/- R+/-, Dox(+) | 22 | 22 | 100 |
Control | H+/- T-/- R+/-, Dox(-) | 25 | 23 | 92 |
Control | H+/- T+/- R-/-, Dox(+) | 32 | 31 | 97 |
Control | H+/- T+/- R-/-, Dox(-) | 31 | 28 | 90 |
Control | H+/- T-/- R-/-, Dox(+) | 15 | 14 | 93 |
Control | H+/- T-/- R-/-, Dox(-) | 19 | 18 | 95 |
NOTE: H+/-, Her2 heterozygous; T+/-, Tam67 heterozygous; R+/-, rtTA heterozygous; Dox, doxycycline. Cutoff time was at 80 wk of age.
When 100% (18 of 18) of group 2 control mice developed mammary tumors, 56% (9 of 16) of group 1 experimental mice developed mammary tumors.