“…This sensitivity is maintained in cells with p16 loss, and although we found some evidence for reduced sensitivity in cells with disabled p53 function, the UCC-derived cell lines were the most refractory, implying that other desensitizing mechanisms are acquired during malignant progression. The three UCC cell lines, RT4, RT112, and EJ, have previously been shown to express EGFR and are therefore suitable candidates for treatment with EGFR inhibitors (32)(33)(34)(35). Although numerous studies have reported an inhibition of proliferation induced by EGFR tyrosine kinase inhibitors in bladder tumor cell lines (34)(35)(36), few studies have investigated the relative effects of inhibitors on normal and malignant-derived cells.…”