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( Division of Human Tumor Biology, Sloan-Kettering Institute for Cancer Research, and Sloan-Kettering Division, Graduate School of Medical Sciences, Cornell University, New York, New York)
The possible roles of host and host immunity in tumor-host-drug interrelationships were studied by comparing the effects of drugs on mouse Sarcoma 180 (S-180) growing singly in nonconditioned mice and rats and singly and bilaterally with human carcinoma H.Ep. #3 in conditioned rats. S-180 grew in 43 per cent of normal rats and in 90100 per cent of rats conditioned with x-radiation and cortisone; generally, larger tumors grew in the latter groups. H.Ep. #3 grew in 86 per cent of the conditioned rats given implants of S-180 bilaterally. Host-conditioning did not modify the antitumor activity of thioguanine and 6-mercaptopurine against S-180 in the rat. The presence of H.Ep. #3 in the same conditioned host likewise had little or no effect on the antitumor activities of azaserine, streptimidone, actinobolin, and 6-diazo-5-oxonorleucine. A comparison of experimental chemotherapy results in conditioned and nonconditioned rats, compared with those obtained in normal mice, indicated that sensitivity of a tumor to a drug remained essentially unchanged under host-conditioning. The use of transplanted tumors in allogeneic and xenogeneic hosts and the possible effects of tumor growth on host immune mechanisms are discussed.
* This study was supported in part by a research grant CY 3784 from the National Cancer Institute, National Institutes of Health, U. S. Public Health Service, Bethesda, Maryland; in part by contract SA-43-ph-1923 and SA-43-ph-2445 from the Cancer Chemotherapy National Service Center, National Cancer Institute, Bethesda, Maryland; and in part by Grant T-47 from the American Cancer Society.
The terminology used here is that suggested by Gorer et al. (10). Briefly, syngeneic = isologous; allogeneic = homologous, and xenogeneic = heterologous.
Received 8/ 2/63.
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