HIGH-FAT DIET BLOCKS THE INHIBITION OF SKIN CARCINOGENESIS AND REDUCTIONS IN PROTEIN-KINASE-C BY MODERATE ENERGY RESTRICTION

Citation
Df. Birt et al., HIGH-FAT DIET BLOCKS THE INHIBITION OF SKIN CARCINOGENESIS AND REDUCTIONS IN PROTEIN-KINASE-C BY MODERATE ENERGY RESTRICTION, Molecular carcinogenesis, 16(2), 1996, pp. 115-120
Citations number
21
Categorie Soggetti
Oncology,Biology
Journal title
ISSN journal
08991987
Volume
16
Issue
2
Year of publication
1996
Pages
115 - 120
Database
ISI
SICI code
0899-1987(1996)16:2<115:HDBTIO>2.0.ZU;2-D
Abstract
The aim of this investigation was to determine the impact of dietary e nergy restriction (ER) with control (C) and high-fat (HF) diets on two -stage skin carcinogenesis and on the expression of specific isoforms of protein kinase C (PKC). Skin carcinogenesis was initiated on SENCAR mice with 10 nmol of 7,12-dimethylbenz[a]anthracene (DMBA) in 0.2 mL of acetone and then promoted with twice weekly treatments of 3.2 nmol of 12-O-tetradecanoylphorbol-13-acetate (TPA) in 0.2 mt of acetone for 18 wk. The experimental diets fed during TPA treatment and for 10 wk after the last TPA treatment were formulated with C (10% calories from fat) and HF (42% calories from fat) levels for freely fed groups. The se diets were restricted by 20% (20% ER/C and 20% ER/HF) and by 40% (4 0% ER/C and 40% ER/HF). Papilloma incidence was reduced in the mice fe d the 20% ER/C 40% ER/C, and 40% ER/HF diets in comparison with the C, I-IF, and 20% ER/HF groups. Carcinoma incidence was also reduced in t hese groups. PKC alpha and zeta were assessed by western blot analysis in the epidermises of mice pre-fed the six diets for 8-10 wk (without DMBA or TPA treatment). PKC alpha was reduced in the particulate frac tion by 32-44% in the 20% ER/C, 40% ER/C, and 40% ER/HF groups (P < 0. 005). PKC zeta was reduced by 24-31% in the cytosol of mice fed the 20 % ER/C diet and in the particulate fraction of mice fed the 40% ER/C d iet (P < 0.05). The HF diet was able to block the inhibition of skin c arcinogenesis and the reduction in the expression of PKC in the epider mis by 20% ER but not by 40% ER. (C) 1996 Wiley-Liss, Inc.