Abstract

Objective To explore the function and mechanism of estrogen receptor α (ERα) in bladder cancer cell proliferation and aggressivity.Methods The ERα expression bladder cancer cell line T24ERα model was established.The cell growth was detected by MTT assay,apoptosis by flow cytometry,cell invasion by matrigel transwell.Western blot was used to check signals by ERα regulation in bladder cancer cells related to the proliferation and metastatic ability.Results Compared to the control group,the cell inhibition rates of experimental group in 96 h and 144 h were 18.85% and 37.21%,respectively.The difference was significant compared with the control group (P < 0.05).The apoptosis rates of the experimental group and control group were (18.93 ±1.41)% and (9.91 ±1.08)% (P<0.05).The experimental group through matrix adhesive cell proportion was (10.00 ± 2.00)%,significantly lower than that of the control group (26.00 ± 3.61) % (P < 0.05).Western blot showed integrin-β1,p-FAK,p-Src and Scr expression were reduced compared to control group (P < 0.05).Conclusion ERα could inhibit bladder cancer cell growth and metastasis through down-regulating integrin-β1-FAK/Src signal pathway,while promote the apoptosis of bladder cancer cells. Key words: Urinary bladder neoplasms; Carcinoma; Estrogen receptor alpha; Cell proliferation; Neoplasm metastasis

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