Table 1.
150 to 330 days
|
150 to 400 days
|
|||
---|---|---|---|---|
Study period Genotype | Pten+/−Irs2+/+ | Pten+/−Irs2−/− | Pten+/−Irs2+/+ | Pten+/−Irs2+/− |
Males (n) | 9 | 9 | 30 | 14 |
Colon cancer | 22% (2) | 0 | 7% (2) | 0 |
Prostate cancer | 22% (2) | 0 | 20% (6) | 29% (4) |
Skin cancer | 11% (1) | 0 | 10% (3) | 0 |
Females (n) | 14 | 10 | 20 | 32 |
Endometrial carcinoma | 7% (1) | 0 | 10% (2) | 6% (2) |
Skin cancer | 14% (2) | 0 | 15% (3) | 9% (3) |
Breast cancer | 21% (3) | 0 | 45% (9) | 19% (6) |
All animals (n) | 23 | 19 | 50 | 46 |
Incidence for invasive neoplasms† | 43% (10) | 0* | 44% (22) | 28% (13) |
The study period ranged from 150 to 330 days to compare Pten+/−Irs2+/+ with Pten+/−Irs2−/− mice and from 150 to 400 days to compare Pten+/−Irs2+/+ with Pten+/−Irs2+/− mice. Pten+/+Irs2+/+ (n = 16) and Pten+/+Irs2−/− (n = 12) controls never developed any neoplasms.
P < 0.001 Fisher’s exact test.
Five mice (one Pten+/−Irs2+/+ male, two Pten+/−Irs2+/+ females, and two Pten+/−Irs2+/− females) had two invasive neoplasms (ie, prostate and skin, breast and skin, or endometrial and breast cancer), which were counted as a single event to calculate incidence.