Table 1.
Mouse Genotype |
Severity of Diseasea |
||||||
---|---|---|---|---|---|---|---|
H | CIN1 | CIN2 | CIN3 | MIC | LIC | ||
cervix | NTG | 17 | 3 | 1 | 2 | ||
E6AP−/− | 2 | 11 | 2 | 1 | 3 | ||
K14E6WTb | 3 | 9 | 7 | 8 | 5 | 7 | |
K14E6WTE6AP−/−c | 1 | 12 | 2 | 1 | |||
vagina | H | VAIN1 | VAIN2 | VAIN3 | MIC | LIC | |
NTG | 16 | 7 | |||||
E6AP−/− | 1 | 18 | |||||
K14E6WTb | 9 | 12 | 15 | 2 | 1 | ||
K14E6WTE6AP−/−c | 5 | 9 | 2 |
Cohorts of female mice of the indicated genotypes were treated with estrogen for 9 months and the reproductive tracts from every mouse was scored for the worst state (severity) of cervical (top half) or vaginal (bottom half of table) disease. The overall severity of disease between different genotypes was compared using a two-sided Wilcoxon-rank sum test. Abbreviations: H, hyperplasia; CIN, cervical intraepithelial hyperplasia; MIC, microinvasive cancer; LIC, large invasive cancer; VAIN, vaginal intraepithelial neoplasia.
The shift in the severity of disease in K14E6WT transgenic mice is highly significant relative to NTG and E6AP−/− mice (p ≪ 0.001).
Loss of E6AP results in a highly significant reduction in the severity of disease in K14E6WTE6AP−/− in the cervix (p≪0.001) and a significant reduction in the vagina (p = 0.05) relative to K14E6WT mice.