In BCPAP cells treated for 72 h, genes from the canonical Wnt pathway (FZD1, DVL1, AKT2, CTNNB1, LEF1, MYC) and the non-canonical Wnt pathway (RHOA, related to cytoskeletal dynamics and increased migration and invasion) were upregulated, suggesting pro-tumor behavior [31,32,33,34]. The gene discussed is MYC; the disease is neoplasm.