TY - JOUR
T1 - A high-tumor-incidence subline of the D1 mouse mammary hyperplastic outgrowth line
T2 - Effect of carcinogens
AU - Ashley, R. L.
AU - Cardiff, Robert
AU - Pratt, T. S.
AU - Faulkin, L. J.
PY - 1982/1/1
Y1 - 1982/1/1
N2 - Mammary tumorigenesis in some mouse strains is characterized by the appearance of a preneoplastic lesion, the hyperplastic alveolar nodule (HAN). The biology of the HAN has been characterized primarily through the study of stable outgrowth lines of serially transplanted HAN. One outgrowth line, DI, which was developed and carried in female BALB/c mice, has been described as a low-tumor-incidence line that does not express murine mammary tumor virus (MuMTV) and is susceptible to hormonal, chemical, and viral carcinogens. In this report, a high-tumor-incidence subline of DI, DI/UCD, is described. Although DI/UCD, like DI, is susceptible to the chemical carcinogen 7,12-dimethylbenz[a]anthracene, an increase in tumor incidence was not observed when DI/UCD outgrowth was exposed to hormones by means of pituitary isografts. Unlike DI, DI/UCD is refractory to the carcinogenic action of MuMTV. Both DI and the DI/UCD subline contained the endogenous MuMTV provirus but did not contain exogenous MuMTV provirus sequences. MuMTV antigen was not detected in DI/UCD outgrowths or tumors. RNA hybridizable to MuMTV complementary DNA was detected in some DI/UCD outgrowths and tumors but did not appear to correlate with tumorigenesis.
AB - Mammary tumorigenesis in some mouse strains is characterized by the appearance of a preneoplastic lesion, the hyperplastic alveolar nodule (HAN). The biology of the HAN has been characterized primarily through the study of stable outgrowth lines of serially transplanted HAN. One outgrowth line, DI, which was developed and carried in female BALB/c mice, has been described as a low-tumor-incidence line that does not express murine mammary tumor virus (MuMTV) and is susceptible to hormonal, chemical, and viral carcinogens. In this report, a high-tumor-incidence subline of DI, DI/UCD, is described. Although DI/UCD, like DI, is susceptible to the chemical carcinogen 7,12-dimethylbenz[a]anthracene, an increase in tumor incidence was not observed when DI/UCD outgrowth was exposed to hormones by means of pituitary isografts. Unlike DI, DI/UCD is refractory to the carcinogenic action of MuMTV. Both DI and the DI/UCD subline contained the endogenous MuMTV provirus but did not contain exogenous MuMTV provirus sequences. MuMTV antigen was not detected in DI/UCD outgrowths or tumors. RNA hybridizable to MuMTV complementary DNA was detected in some DI/UCD outgrowths and tumors but did not appear to correlate with tumorigenesis.
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M3 - Article
C2 - 6287083
AN - SCOPUS:0019970511
VL - 69
SP - 639
EP - 645
JO - Journal of the National Cancer Institute
JF - Journal of the National Cancer Institute
SN - 0027-8874
IS - 3
ER -