Combined use of anti-VEGF and Anti-EGFR monoclonal antibodies with Photodynamic therapy suppresses tumor growth in an in vivo tumor model

Abstract

Photodynamic therapy (PDT) is a promising treatment option for only cancer. It can be used to treat drugresistant and inoperable tumors. However, one of the unsolved problems in PDT is tumor recurrence. The aim of this study is to suppress tumor regrowth by including angiogenesis inhibitors that target vascular endothelial growth factor (VEGF) and epidermal growth factor receptor (EGFR) pathways, to the PDT protocol. Human bladder cancer (MGH cell line) xenografts were induced in Balb/c nude mice. The animals treated with PDT received an intravenous injection of hypericin followed by irradiation after 6 hours, with a broadband light source through a 560-640 NM band-pass filter. A light dosage of 120 J/cm2 and 100 mW/cm2 was administered. Angiogenesis inhibitors, bevacizumab and cetuximab were administered at a dose of 10 mg/kg. Treatment efficacy was assessed by monitoring the tumor growth inhibition of xenograft tumors. Immunohistochemistry was performed to evaluate the expression of VEGF and EGFR. Expression of the major proteins in the VEGF and EGFR pathways was investigated by immunoblotting. One-way ANOVA with Bonferroni correction was performed to analyze the data. Tumors treated with the combination of PDT and inhibitors exhibited significantly greater treatment response compared to control and PDT groups. Downregulation of VEGF and EGFR was observed in tumors treated with PDT + bevacizumab and cetuximab. Our results show that blocking VEGF or/and EGFR pathways along with PDT can effectively suppress tumor growth. © 2013 Bhuvaneswari R, et al.