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Oncol Rep ; 8(2): 445-9, 2001.
Article in English | MEDLINE | ID: mdl-11182072

ABSTRACT

This study links the tumor inhibitory effect of anti-progestins RU486 and ZK98299 to the expression of cell cycle proteins. Medroxyprogesterone acetate-induced ductal mammary adenocarcinoma-bearing female BALB/c mice were treated daily either with RU486 or ZK98299, observing tumor growth retardation. p21 increased after 24 h treatment, peaked at day 4 and returned to control levels at day 7. Cyclin D1, cyclin E, CDK2 and CDK4, did not change during treatment. These results suggest that p21 might play a role in early inhibitory stages of tumor growth induced by RU486 and ZK98299.


Subject(s)
CDC2-CDC28 Kinases , Cell Cycle Proteins/analysis , Gonanes/therapeutic use , Hormone Antagonists/therapeutic use , Mammary Neoplasms, Experimental/drug therapy , Mifepristone/therapeutic use , Proto-Oncogene Proteins , Animals , Antineoplastic Agents/therapeutic use , Cell Division/drug effects , Cyclin D1/analysis , Cyclin E/analysis , Cyclin-Dependent Kinase 2 , Cyclin-Dependent Kinase 4 , Cyclin-Dependent Kinase Inhibitor p21 , Cyclin-Dependent Kinases/analysis , Cyclins/analysis , Enzyme Inhibitors/analysis , Female , Mammary Neoplasms, Experimental/pathology , Mice , Mice, Inbred BALB C , Protein Serine-Threonine Kinases/analysis , Time Factors
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