Among the identified targets, CHN1 attracted our attention for following reasons: (i) there were two binding sites for miR-205 in the 3’UTR of CHN1, one of which was highly conserved among different species (Fig. 2a); and (ii) CHN1 has been reported to be a cancer-associated gene [26] involved in cell migration and cancer cell motility [24, 28]. This evidence concerns the gene CHN1 and cancer.