Biochemical and Biophysical Research Communications, Vol.377, No.2, 720-724, 2008
Aberrant methylation of human L- and M-fructose 1,6-bisphosphatase genes in cancer
A possible epigenetic regulation of the two isoenzymes of fructose 1,6-bisphosphatase (FBPase) was studied in liver, muscle, mamma, breast cancer and in different cancer cell lines. Results obtained after bisulfite sequencing revealed a different CpG methylation of both promoters in liver, muscle and breast tissue which is putatively involved in the cell-type specific gene expression of the two enzymes. In tumor cell lines, demethylation with 5-aza-deoxycytidine activated the expression of both isoenzymes. Additional inhibition of histone deacetylase with trichostatin A further increased FBPase mRNA concentrations. Since cancers typically have an abnormal energy metabolism and exhibit a low gluconeogenic phenotype, it was studied whether promoter methylation contributes to the decreased expression of FBPase in breast cancer. When non-malignant and malignant tissue samples from the same patient were compared a correlation between an increase of FBPase promoter methylation and a decrease of FBPase mRNA levels was observed. (C) 2008 Elsevier Inc. All rights reserved.
Keywords:Breast cancer;Cell line;DNA methylation;Fructose 1,6-bisphosphatase;Gene expression;Gluconeogenesis;Promoter;Tissue-specific expression