We studied the effects of tamoxifen (TAM) on the growth of 7,12-dimethylbenz(a)anthracene (DMBA)-induced rat mammary tumor and the expression of cyclin DI, cyclin E, p21(Cip1), and estrogen receptors (ER) by performing immunohistochemistry and Western blot analysis. When tumor size reached between 10 and 15 nim. in the largest dimension, the rats were divided into a DMBA-control group and a DMBA-TAM group. The administration of TAM markedly decreased the tumor development and showed decreased expression of bromodeoxyuridine, cyclin D1, cyclin E, and p21(Cip1) when compared with those of the DMBA-control group; however, a few tumors showed progressive growth in spite of TAM treatment. These tumors had decreased expression of ER. This study suggests that TAM suppresses tumor development through the down-expression of cyclin D1 and cyclin E. (C) 2001 Elsevier Science Ireland Ltd. All rights reserved.
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Department of Nutritional Sciences, Faculty of Medicine, 150 College St, TorontoDepartment of Nutritional Sciences, Faculty of Medicine, 150 College St, Toronto
Korkola J.E.
Wood G.A.
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Department of Nutritional Sciences, Faculty of Medicine, 150 College St, TorontoDepartment of Nutritional Sciences, Faculty of Medicine, 150 College St, Toronto
Wood G.A.
Archer M.C.
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Department of Nutritional Sciences, Faculty of Medicine, 150 College St, TorontoDepartment of Nutritional Sciences, Faculty of Medicine, 150 College St, Toronto