Some tissues of tumor-bearing animals, particularly the liver, are known to differ from the corresponding normal tissues in the levels of certain enzyme activities and the concentrations of associated metabolically active components (1-8). Furthermore, the administration of fractions obtained from tumors to normal animals can elicit similar changes (9-1 l), but it is not yet clear to what degree such changes in host tissues represent the effects of specific directive substances released by the tumor. Some of the reported changes may reflect the pathologic alterations associated with the general deterioration of the host in advanced stages of cancer. Many of the reported changes in host tissues were seen in animals bearing large tumors, so that the metabolic activities of the tumor represented a major part of the host's total metabolism, and the changes in host tissues may have reflected adjustments to the competition and metabolic burdens imposed by the presence of the tumor (12).We have studied the levels of enzyme activities in the livers of hepatoma-bearing rats during a period when the tumor was still small, to minimize the influence of general tumor metabolism per se.' The parameters chosen for study included activities that are associated with various cytoplasmic compartments and that in some hepatomas are present at levels different from the levels in normal liver. The relatively slow-growing transplantable Reuber H-35 hepatoma (13) was used so that tumor effects could be studied for an extended period during which the tumor size did not exceed a small percent of the host animal's body weight. The changes from normal liver in host liver and in tumor were determined, and where the host liver showed significant changes from normal liver, the time course of the changes was followed in host liver during the period of early tumor growth. Controls involving transplants of normal liver were also run to further define the specificity of tumor effects on the host livers. Growing animals were used with the expectation that tumor effects might become discernible sooner than in adult animals.Materials and methods. Female ACl strain rats were obtained from Microbiological Associates at about 4 weeks of age and 70 g weight, and were maintained in our laboratory on a diet of Purina rat pellets and water ad libitum. The Reuber H-35 hepatoma, obtained from a tumor-bearing rat kindly supplied to us by Dr. Melvin Reuber, was maintained in our laboratory by serial transplants in female AC1 rats. Tumors weighing 4-8g were trimmed free of necrotic tissue, minced in sterile 0.9% NaCl solution, and 0.5 ml of mince, containing 100 mg tumor, was implanted by trochar subcutaneously on the back of rats weighing 100-1 15 g and about 6 weeks of age. Some animals received similar implants of minced liver taken from a normal female AC1 rat of the same age. Normal control animals of the same age and weight were injected with 0.9% NaCl solution. The animals were routinely weighed three times a week and just before killing, and tumor sizes ...