Cancer Research The Future of Cancer Research: Science and Patient Impact  Tumor Immunology: New Perspectives
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Cancer Research Clinical Cancer Research
Cancer Epidemiology Biomarkers & Prevention Molecular Cancer Therapeutics
Molecular Cancer Research Cancer Prevention Research
Cancer Prevention Journals Portal Cancer Reviews Online
Annual Meeting Education Book Meeting Abstracts Online

[Cancer Research 24, 114-119, January 1, 1964]
© 1964 American Association for Cancer Research

This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Teller, M. N.
Right arrow Articles by Wagshul, S. F.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Teller, M. N.
Right arrow Articles by Wagshul, S. F.

Host-Tumor-Drug Relationships in Experimental Chemotherapy Systems with Allogeneic and Xenogeneic Host-Tumor Combinations*

M. N. Teller, R. Wolff and S. F. Wagshul

( 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 90–100 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.





HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Cancer Research Clinical Cancer Research
Cancer Epidemiology Biomarkers & Prevention Molecular Cancer Therapeutics
Molecular Cancer Research Cancer Prevention Research
Cancer Prevention Journals Portal Cancer Reviews Online
Annual Meeting Education Book Meeting Abstracts Online
Copyright © 1964 by the American Association for Cancer Research.