The influence of morin hydrate on changes of proliferative, metastatic, and adhesive potential of human ovarian cancer cells concerning the influence of decitabine, and decitabine with trichostatin A, and in comparison to untreated cells, were analyzed. The effect of morin hydrate, decitabine, and trichostatin A were examined in A2780 and SKOV-3 ovarian cancer cell lines using MTS assay, clonogenic assay, adhesion to endothelial HMEC-1 cells, transwell migration assay and cell cycle analysis. The expression level of epithelial to mesenchymal transition (EMT) markers was quantified using PCR Array in relation to the level of global methylation determined with Methylated DNA Quantification Kit. We observed statistically significant inhibition of adhesive and migratory potential of both cell lines and the accumulation of G0/G1 phase A2780 cells after treatment with morin hydrate. Our studies confirmed the influence of morin hydrate on down-regulation of genes considered as up-regulated during EMT, and up-regulation of some genes considered as down-regulated during EMT in A2780 and SKOV-3 cells. Phenotypic changes were associated with molecular changes in cells, eg. decrease of the expression level of genes associated with adhesion, and an increase of genes down-regulated during EMT, after morin hydrate treatment in comparison to untreated control cells in both cell lines, were observed. Keywords Adhesion • Epithelial to mesenchymal transition • Metastasis • Morin hydrate • Ovarian cancer cells Abbreviations ATCC American type culture collection DNMT DNA methyltransferase ECACC European collection of authenticated cell cultures ECM Extracellular matrix EMT Epithelial to mesenchymal transition EOC Epithelial ovarian cancer HAT Histone acetyltransferase HDAC Histone deacetylase MET Mesenchymal to epithelial transition SAM S-sdenosyl-l-methionine TSA Trichostatin A