SUMMARY.-The histone, neutral and acidic nuclear-protein content of BR6 mouse mammary tumours have been measured and related to growth rate and hormone responsiveness. In unresponsive tumours, histone and neutral nuclear-protein content was inversely correlated with growth rate while acidic nuclear-proteins were directly correlated with growth rate. The histone content of these tumours was low when compared to pregnancy dependent tumours growing at the same rate under the same physiological conditions.In vitro incorporation of labelled amino acids into total protein and the nuclear proteins was also measured. Pregnancy independent tumours had higher rates of total protein synthesis than pregnancy dependent tumours. The rates of incorporation of amino acids into the nuclear proteins also tended to be higher in independent tumours.RECENT studies of hormone responsive and unresponsive tumours in a variety of species have indicated that the latter tend to be metabolically more active in that they have higher enzyme activities, co-factor concentrations, rates of glycolysis and respiration (King, 1968). In view of current speculation about the role of nuclear proteins in the control of metabolism (Bonner and Ts'o, 1964; Paul and Gilmour, 1968) differences in the nuclei of such tumours may be worth consideration. The amounts of basic (histone), acidic, and neutral nuclear proteins have therefore been measured in the nuclei of spontaneous, pregnancy dependent and independent mammary tumours in BR6 mice. The in vitro rates of incorporation of amino acids into these proteins, and into total protein, have also been estimated. The possible influence of growth rate on the results has been considered.
MATERIALS AND METHODSTumours.-Spontaneous BR6 mouse mammary tumours were obtained from pregnant and non-pregnant mice. The characteristics of these tumours have been described previously (Foulds, 1949). Tumours which had appeared two or three times during successive pregnancies and had regressed to less than 50% of their maximum size within 5 days of parturition were considered pregnancy dependent. These were obtained from pregnant mice, 17-20 days after mating. Independent tumours were those known to grow in non-pregnant mice. Such tumours arise by a gradual or rapid loss of dependence on pregnancy for growth (Foulds, 1949). Pregnancy independent tumours were obtained from pregnant and non-pregnant mice.