The most common malignancy in the urinary system has been bladder cancer (
1) that has suggested that this malignancy was a main cause of cancer morbidity or mortality (
2). Bladder cancer has been the ninth most common cancer in all over the world (
1). In western countries, the most predominant histologic subtype in urothelial system has been transitional cell carcinoma (TCC) (urothelial carcinoma) (
3). Genetic abnormalities and environmental exposures were responsible for most causes of this malignancy (
4). Overexpression of some growth factors, such as epidermal growth factor receptor (EGFR), has mentioned in many tumors like gliomas, pancreatic, colorectal, breast, head and neck, lung, prostate, ovary, advanced gastric cancer, and urothelial carcinoma (
5-
7). In many contexts, it has reported that EGFR family encoded by oncogenes c-erb. These receptors have belonged to the group of receptors that all have encoded by these oncogenes. Human epidermal receptors (HER), family of tyrosine kinases receptors were four different receivers. Loss of coordination for cell growing by pathological expression of c-erbB oncogenes, could lead to malignancies. Motility, angiogenesis, invasion and metastasis all together were the results of EGFR expression (
8-
11). The higher stage or grade of bladder cancer has expected with more expression of EGFR, thus eventually progression of carcinoma has caused poor prognosis (
12-
19). Also for anti-tumor effects, one could inhibit these pathways. Inhibition of EGFR1 and HER2 might have effective results for their antitumor activity because numerous bladder tumors expressed the EGFR family (
20).