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Chemopreventive efficacies of rosiglitazone, fenretinide and their combination against rat mammary carcinogenesis

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Abstract

Introduction

Peroxisome proliferator-activated receptor gamma (PPAR-γ) and retinoic acid receptors (RAR/RXR) belong to the nuclear steroid receptor family. In vitro studies have suggested that PPAR-γ ligands are highly effective in preventing mammary tumours and these effects are enhanced by some retinoids. However, in vivo anti-initiator and anti-promoter efficacies of this combination are not clear.

Aim and methods

The present study aimed to investigate the chemopreventive efficacies of the PPAR-γ ligand rosiglitazone (200 μg/kg/day), synthetic retinoid fenretinide (0.3 mg/kg/day) and their combination on a DMBA-induced rat mammary carcinogenesis model.

Results

In the rosiglitazone group, no malignant tumour developed, apart from the lowest proliferative mammary lesions. In the fenretinide group, 30% developed a malignant tumour but there were no benign tumours. Cancer incidences were 61.5% and 10% in the control and combination groups respectively.

Conclusions

Our results showed that the PPAR-γ ligand rosiglitazone and synthetic retinoid fenretinide have potent chemopreventive properties against in vivo mammary carcinogenesis; however, the efficacies were not enhanced by their combination.

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Correspondence to Hilal Kocdor.

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Kocdor, H., Kocdor, M.A., Canda, T. et al. Chemopreventive efficacies of rosiglitazone, fenretinide and their combination against rat mammary carcinogenesis. Clin Transl Oncol 11, 243–249 (2009). https://doi.org/10.1007/s12094-009-0347-5

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  • DOI: https://doi.org/10.1007/s12094-009-0347-5

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