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. 2003 Aug;23(16):5738–5754. doi: 10.1128/MCB.23.16.5738-5754.2003

TABLE 1.

Tumor incidence and histopathology in female MMTV-c-rel transgenic mice after multiple cycles of pregnancy and regressiona

Mam. tumor diagnosis (other tumors)b Agec (mo) No. of:
Line Mouse no.d
Mam. tumors Other tumors
Mam. squamous cell carcinoma and hyperplasia (bronchial adenocarcinoma) 22 1 1 7 4026
Mam. adenosquamous carcinoma 22 1 0 7 4042
Mam. adenosquamous carcinoma 18 1 0 14 3814
Mam. adenosquamous carcinoma (papillary bronchial adenomas) 20 1 1 14 3983
Mam. adenocarcinomas with pulmonary metastases 23 4 1 14 3996
Mam. papillary carcinoma, lobular hyperplasia, squamous nodules 23 1 0 14 4936
Mam. squamous cell carcinoma and hyperplasia 15 1 0 14 4556
Mam. adenocarcinoma (papillary bronchial adenocarcinomas) 19 1 1 15 127
Mam. squamous cell carcinoma 22 1 0 16 3872
Mam. adenocarcinoma with poorly differentiated large cells 18 1 0 16 3875
Mam. squamous cell carcinoma and hyperplasia (centrocytic lymphoma) 18 1 1 16 4521
Spindle cell tumor, originating from a mam. adenocarcinoma 19 1 0 16 4528
a

Thirty-eight multiparous female mice from the four transgenic lines (7, 14, 15, and 16) were monitored for tumor incidence by biweekly palpable examination.

b

Histopathological analysis of mammary (mam.) glands and other organs (heart, lung, liver, kidney, spleen, and adrenal gland) from the same animal was performed when a tumor was detected.

c

Age when tumor was detected.

d

An identification number was given to the individual mice of the cohort for further analysis of the tumors.