Further characterization reveals that knockdown of DDX3 is associated with overexpression of DNMT3A and down-regulation of tumor-suppressive miR-200b, miR-200c, miR-122 and miR-145 through enriched DNMT3A binding and enhanced cytosine methylation as well as H3K27me3 elevation on promoter regions of these tumor-suppressive miRNAs. Here, DDX3X is linked to neoplasm.