Abstract | PURPOSE: EXPERIMENTAL DESIGN: For prevention, mice were fed a powdered control diet, the SERM arzoxifene (Arz, 20 mg/kg diet), the rexinoid LG100268 (268, 30 mg/kg diet), or the combination for 60 weeks. In a second prevention study, mice were fed Arz (6 mg/kg diet), 268 (30 mg/kg diet), the combination of Arz and 268, the SERM acolbifene (Acol, 3 mg/kg diet), or the combination of Acol and 268 for 52 weeks. For the treatment studies, mice with tumors were fed combinations of a SERM and 268 for 4 weeks. RESULTS: The rexinoid 268 and the SERMs Arz and Acol, as individual drugs, delayed the development of estrogen receptor-negative tumors. Moreover, the combination of a SERM and 268 was strikingly synergistic, as no tumors developed in any mouse fed the combination of 268 and a SERM. Moreover, this drug combination also induced significant tumor regression when used therapeutically. These drugs did not inhibit transgene expression in vitro or in vivo, and the combination of Arz and 268 inhibited proliferation and induced apoptosis in the tumors. CONCLUSION: The combination of a rexinoid and SERM should be considered for future clinical trials.
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Authors | Karen Liby, Mara Rendi, Nanjoo Suh, Darlene B Royce, Renee Risingsong, Charlotte R Williams, William Lamph, Fernand Labrie, Stan Krajewski, Xiaochun Xu, Heetae Kim, Powel Brown, Michael B Sporn |
Journal | Clinical cancer research : an official journal of the American Association for Cancer Research
(Clin Cancer Res)
Vol. 12
Issue 19
Pg. 5902-9
(Oct 01 2006)
ISSN: 1078-0432 [Print] United States |
PMID | 17020999
(Publication Type: Comparative Study, Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)
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Chemical References |
- Nicotinic Acids
- Piperidines
- Receptors, Estrogen
- Selective Estrogen Receptor Modulators
- Tetrahydronaphthalenes
- Thiophenes
- ritetronium
- LY 353381
- LG 100268
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Topics |
- Animals
- Cell Division
(drug effects)
- Disease Models, Animal
- Drug Synergism
- Drug Therapy, Combination
- Female
- Humans
- Mammary Neoplasms, Experimental
(drug therapy, pathology, prevention & control)
- Mice
- Mice, Transgenic
- Nicotinic Acids
(therapeutic use)
- Piperidines
(therapeutic use)
- Receptors, Estrogen
(metabolism)
- Selective Estrogen Receptor Modulators
(pharmacology)
- Survival Rate
- Tetrahydronaphthalenes
(therapeutic use)
- Thiophenes
(therapeutic use)
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