The aim of the present study was to evaluate the in vivo effects of the RAR-a selective antagonist Ro 41-5253 on a xenograft animal model for breast cancer. Our observations indicate a lack of toxic side effects of the drug, even when used at high dosages. It is interesting to note that using Ro 41-5253 at dosages of 10, 30 and 100 mg/kg/die resulted in a slight, but significant inhibition of cell growth. The data obtained in this study represents the basis for a further evaluation of Ro 41-5253 anti-neoplastic activity on transgenic breast cancer animal models. q 2004 Elsevier Ireland Ltd. All rights reserved.
Retinoids and human breast cancer: in vivo effects of an antagonist for RAR-a.
RAVERA, GIAMBATTISTA;
2005-01-01
Abstract
The aim of the present study was to evaluate the in vivo effects of the RAR-a selective antagonist Ro 41-5253 on a xenograft animal model for breast cancer. Our observations indicate a lack of toxic side effects of the drug, even when used at high dosages. It is interesting to note that using Ro 41-5253 at dosages of 10, 30 and 100 mg/kg/die resulted in a slight, but significant inhibition of cell growth. The data obtained in this study represents the basis for a further evaluation of Ro 41-5253 anti-neoplastic activity on transgenic breast cancer animal models. q 2004 Elsevier Ireland Ltd. All rights reserved.
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