We further verified that ERBB3 repression suppressed the EMT phenotype of T24 and UM-UC-3 cells at least partially by regulating AKT2/Snail signaling, which was consistent with previous experiments.14 In addition, ERBB3 repression inhibited bladder cancer proliferation via cell cycle regulation. The gene discussed is AKT2; the disease is urinary bladder carcinoma.