TY - JOUR
T1 - Mouse mammary tumor virus infections
T2 - Viral expression and tumor risk
AU - Altrock, Bruce W.
AU - Cardiff, Robert
PY - 1979/1/1
Y1 - 1979/1/1
N2 - Concentrations of murine mammary tumor virus (MuMTV) antigen in the milk of Individual naturally infected BALB/cfC3H and BALB/c mice given injections of MuMTV were related to their risk of developing a mammary tumor. Two distinct groups of MuMTV-infected mice were Identified. One group exhibited high viral antigen levels in their milk (>100 MO/ml), whereas the other group exhibited low viral antigen levels in their milk (≥3 μg/ml). Mice that exhibited high levels developed tumors by 17 months of age, whereas those with low levels did not. Viral expression levels in mice having high risks of tumor development were also related to the length of the latency period preceding overt tumor development. The tumor risk potential of naturally infected mice was frequently that of their mothers. Various doses of MuMTV were Injected into BALB/c mice, and the resulting infections differed in latency period, level of viral expression, and potential for neoplastic transformation.—JNCI 63: 1075–1080, 1979.
AB - Concentrations of murine mammary tumor virus (MuMTV) antigen in the milk of Individual naturally infected BALB/cfC3H and BALB/c mice given injections of MuMTV were related to their risk of developing a mammary tumor. Two distinct groups of MuMTV-infected mice were Identified. One group exhibited high viral antigen levels in their milk (>100 MO/ml), whereas the other group exhibited low viral antigen levels in their milk (≥3 μg/ml). Mice that exhibited high levels developed tumors by 17 months of age, whereas those with low levels did not. Viral expression levels in mice having high risks of tumor development were also related to the length of the latency period preceding overt tumor development. The tumor risk potential of naturally infected mice was frequently that of their mothers. Various doses of MuMTV were Injected into BALB/c mice, and the resulting infections differed in latency period, level of viral expression, and potential for neoplastic transformation.—JNCI 63: 1075–1080, 1979.
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U2 - 10.1093/jnci/63.4.1075
DO - 10.1093/jnci/63.4.1075
M3 - Article
C2 - 225501
AN - SCOPUS:0018693061
VL - 63
JO - Journal of the National Cancer Institute
JF - Journal of the National Cancer Institute
SN - 0027-8874
IS - 4
ER -