“…Many genes have been identified as being putatively regulated by WT1(tumor suppressor gene, mutations of which are involved in tumor genesis of Wilms' tumor) including E-cadherin [12], insulin-like growth factor II [13], insulin-like growth factor I receptor [14], plateletderived growth factor A-chain [15,16], syndecan, Pax-223 [17], Dax I [18], amphiregulin [19], and β-catenin [20][21][22]. However, it is still not clear what the biologically critical targets for WT1 regulation are, and the cellular pathways abrogated as a result of WT1 mutations are yet to be identified.…”