Cancer Research Infection and Cancer: Biology, Therapeutics, and Prevention  Cancer Health Disparities Conference 2009
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 56, 1724-1726, April 15, 1996]
© 1996 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 McCormick, D. L.
Right arrow Articles by Kelloff, G. J.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by McCormick, D. L.
Right arrow Articles by Kelloff, G. J.

Exceptional Chemopreventive Activity of Low-Dose Dehydroepiandrosterone in the Rat Mammary Gland1

David L. McCormick2, Kandala V. N. Rao, William D. Johnson, Teresa A. Bowman-Gram, Vernon E. Steele, Ronald A. Lubet and Gary J. Kelloff

Life Sciences Department. IIT Research Institute, Chicago, Illinois 60616 [D. L. M., K. V. N. R., W. D. J., T. A. B-G.], and Chemoprevention Investigational Studies Branch, National Cancer Institute, Bethesda, Maryland 20852 [V. E. S., R. A. L., G. J. K.]

To determine if the chemopreventive activity of dehydroepiandrosterone (DHEA) in the rat mammary gland can be dissociated from its toxicity, two studies were conducted in which low doses of DHEA were administered alone and in combination with other agents to rats treated with N-methyl-N-nitrosourea. Beginning 1 week prior to administration of 35 mg N-methyl-N-nitrosourea per kg body weight, groups of 20 female Sprague-Dawley rats were fed AIN-76A diet supplemented with DHEA alone (800 or 400 mg/kg diet), DHEA + tamoxifen (80 or 40 µg/kg diet), DHEA + carbenoxolone (3500 or 1750 mg/kg diet), or DHEA + tamoxifen + carbenoxolone. When administered alone at either 800 or 400 mg/kg diet, DHEA reduced mammary cancer incidence from >70% in dietary controls to 0%; mammary cancer incidence in all DHEA combination regimens was also ≤5%. The dose levels of DHEA used induced no toxicity or alteration in body weight gain. These results indicate that dietary supplementation with low doses of DHEA has chemopreventive efficacy greater than or equal to that of endocrine ablation. This protection may be mediated by the induction of differentiation in the mammary parenchyma.

1 Research supported by contract N01-CN-85097-11 and Grant CA-30646 from the National Cancer Institute, Department of Health and Human Services.

2 To whom requests for reprints should be addressed, at Life Sciences Department, IIT Research Institute, 10 West 35th Street, Chicago, IL 60616.

Received 1/22/96. Accepted 2/29/96.




This article has been cited by other articles:


Home page
CarcinogenesisHome page
D. L. McCormick, W. D. Johnson, N. M. Kozub, K.V.N. Rao, R. A. Lubet, V. E. Steele, and M. C. Bosland
Chemoprevention of rat prostate carcinogenesis by dietary 16{alpha}-fluoro-5-androsten-17-one (fluasterone), a minimally androgenic analog of dehydroepiandrosterone
Carcinogenesis, February 1, 2007; 28(2): 398 - 403.
[Abstract] [Full Text] [PDF]


Home page
Endocr Relat CancerHome page
F Labrie
Future perspectives of selective estrogen receptor modulators used alone and in combination with DHEA.
Endocr. Relat. Cancer, June 1, 2006; 13(2): 335 - 355.
[Abstract] [Full Text] [PDF]


Home page
Cancer Res.Home page
H. P. Ciolino, C. J. MacDonald, and G. C. Yeh
Inhibition of Carcinogen-activating Enzymes by 16{alpha}-Fluoro-5-androsten-17-one
Cancer Res., July 1, 2002; 62(13): 3685 - 3690.
[Abstract] [Full Text] [PDF]


Home page
Exp. Biol. Med.Home page
K. P. Nephew, E. Osborne, R. A. Lubet, C. J. Grubbs, and S. A. Khan
Effects of Oral Administration of Tamoxifen, Toremifene, Dehydroepiandrosterone, and Vorozole on Uterine Histomorphology in the Rat
Experimental Biology and Medicine, March 1, 2000; 223(3): 288 - 294.
[Abstract] [Full Text]


Home page
J. Biol. Chem.Home page
H. P. Ciolino and G. C. Yeh
The Steroid Hormone Dehydroepiandrosterone Inhibits CYP1A1 Expression in Vitro By a Post-transcriptional Mechanism
J. Biol. Chem., December 3, 1999; 274(49): 35186 - 35190.
[Abstract] [Full Text] [PDF]


Home page
Cancer Res.Home page
K. V. N. Rao, W. D. Johnson, M. C. Bosland, R. A. Lubet, V. E. Steele, G. J. Kelloff, and D. L. McCormick
Chemoprevention of Rat Prostate Carcinogenesis by Early and Delayed Administration of Dehydroepiandrosterone
Cancer Res., July 1, 1999; 59(13): 3084 - 3089.
[Abstract] [Full Text] [PDF]




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 © 1996 by the American Association for Cancer Research.