Genomic methylation patterns of Dunning R-3327 cell lines anaplastic t
umor-1 (AT-1), anaplastic tumor-3 (AT-3), metastasis-lymph and lung (M
at-LyLu) and metastasis-lung (Mat-Lu), and Mat-LyLu cells treated with
difluoromethylornithine (DEMO), and retinoic acid (RA) have been anal
yzed. Each cell line was digested with HpaII and MspI restriction endo
nuclease enzymes to characterize methylation patterns, at the interior
cytosine of the sequence C(m)CGG. Identical molecular weight banding
patterns were found for both HpaII and MspI digests in normal dorsal p
rostate (NDP) used as a control. Both the treated and non-treated Dunn
ing R-3327 cells digested with HpaII and MspI, displayed similar bandi
ng profiles from those seen in NDP solid tissues, indicative of a prog
ressive loss of methylation at CCGG sites.