Skip to main content
. 1999 Mar 30;96(7):3916–3921. doi: 10.1073/pnas.96.7.3916

Table 1.

Conditional suppression of neuroendocrine carcinogenesis by expression of an RB transgene in Rb+/− mice

Neoplasia Rb+/−mice with tumor (%)*
Rb+/−RTgRB mice with tumor (%)
Fisher’s P Tet(−) vs. Tet(+)
Moribund P140§ Tet(−) Tet(+)
Melanotroph tumor of the pituitary 100  (41/41) 100  (10/10) 25  (3/12) 100  (11/11) 0.0003
Tumor of the pituitary anterior lobe 22  (9/41) 19  (5/27) ND ND
C-cell thyroid carcinoma 95  (36/38) 100  (7/7) 17  (2/12) 91  (10/11) 0.006
Parathyroid adenoma 8  (3/39) ND ND ND
C-cell lung metastases 68  (26/38) 0  (0/11) ND ND
Lung neuroendocrine hyperplasia 11  (4/38) ND ND ND
Adrenal pheochromocytoma 71  (22/31) 78  (7/9) 25  (3/12) 73  (8/11) 0.0391
Islet of Langerhans hyperplasia 41  (7/17) ND ND ND
*

Numbers in parentheses indicate number of mice with tumor out of total number of mice. 

Rb+/− mice in which expression of an RB transgene is repressed by tetracycline (Fig. 2); animals were treated with tetracycline from fertilization until either P90, Tet(−), or P140, Tet(+), killed on P140, and scored for tumors. ND, not determined. According to immunohistochemical and Western blotting analyses, no expression of RB was detected in tumors developing in Tet(−) group of Rb+/−RTgRB mice. 

No significant difference in the frequencies of tumors was observed between Rb+/− mice and Rb+/− mice with either TgRBp-tTA or TghCMV*-1p-RB. 

§

Both invasive tumors and EAPs are included.