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 41, 3863-3867, October 1, 1981]
© 1981 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 HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Miller, F. R.
Right arrow Articles by Heppner, G. H.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Miller, F. R.
Right arrow Articles by Heppner, G. H.

Preferential Growth of Mammary Tumors in Intact Mammary Fatpads1

Fred R. Miller2, Daniel Medina and Gloria H. Heppner

Department of Immunology, Michigan Cancer Foundation, Detroit, Michigan 48201 [F. R. M., G. H. H.] and Department of Cell Biology, Baylor College of Medicine, Houston, Texas 77025 [D. M.]

Four transplantable mammary tumors, three (66, 410, and 168cl) isolated from a spontaneously occurring strain BALB/cfC3H mammary tumor and one (D2) arising from a BALB/c hyperplastic alveolar nodule were found to grow better in mammary fatpads than at s.c. sites. Furthermore, tumor growth was better (p < 0.05) in intact mammary glands than in cleared mammary fatpads for the D2, 410, and 66 tumors (168cl was not tested). The role of immunity in these differences was investigated using the highly immunogenic 410 tumor. Tumor 410 induced equally effective immunity to subsequent challenge whether it was implanted s.c. or in intact fatpads. Furthermore, in immunized animals, Tumor 410 was rejected equally well when the challenge site was intact fatpad as when s.c. Similarly, Tumor 410 induced immunity after implantation into cleared fatpads and, in immunized animals, was rejected when the challenge site was the cleared fatpad. We thus found no evidence that the mammary fatpad is immunologically privlleged, as compared to the s.c. site, with respect to tumor transplantation antigens.

1 This work was supported by USPHS Grants CA 22453, CA 27437, and CA 28366 and by a grant from the Concern Foundation.

2 To whom requests for reprints should be addressed, at the Department of Immunology, Michigan Cancer Foundation, 110 E. Warren Ave., Detroit, Mich. 48201.

Received 4/20/81. Accepted 6/23/81.




This article has been cited by other articles:


Home page
Cancer Res.Home page
R. Munoz, S. Man, Y. Shaked, C. R. Lee, J. Wong, G. Francia, and R. S. Kerbel
Highly Efficacious Nontoxic Preclinical Treatment for Advanced Metastatic Breast Cancer Using Combination Oral UFT-Cyclophosphamide Metronomic Chemotherapy.
Cancer Res., April 1, 2006; 66(7): 3386 - 3391.
[Abstract] [Full Text] [PDF]


Home page
Mol. Cell. Biol.Home page
A. K. Man, L. J. T. Young, J. A. Tynan, J. Lesperance, M. Egeblad, Z. Werb, C. A. Hauser, W. J. Muller, R. D. Cardiff, and R. G. Oshima
Ets2-Dependent Stromal Regulation of Mouse Mammary Tumors
Mol. Cell. Biol., December 1, 2003; 23(23): 8614 - 8625.
[Abstract] [Full Text] [PDF]


Home page
J. Cell Sci.Home page
K. L. Schmeichel and M. J. Bissell
Modeling tissue-specific signaling and organ function in three dimensions
J. Cell Sci., June 15, 2003; 116(12): 2377 - 2388.
[Abstract] [Full Text] [PDF]


Home page
Genes Dev.Home page
B. Elenbaas, L. Spirio, F. Koerner, M. D. Fleming, D. B. Zimonjic, J. L. Donaher, N. C. Popescu, W. C. Hahn, and R. A. Weinberg
Human breast cancer cells generated by oncogenic transformation of primary mammary epithelial cells
Genes & Dev., January 1, 2001; 15(1): 50 - 65.
[Abstract] [Full Text]




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 © 1981 by the American Association for Cancer Research.