Abstract

Recent research has attempted to direct superantigens towards tumors by means of tumor-targeted superantigen (TTS) strategy. In this study, we explored the antitumor property of TTS by fusing the third loop of transforming growth factor alpha (TGF alpha L3) to staphylococcal enterotoxin type B (SEB) and investigated the possibility of the therapeutic application of TGF alpha L3-SEB as a novel antitumor candidate in mice bearing breast cancer. Treatment was performed through intratumoral and intravenous injection of TGF alpha L3-SEB. Tumor size/volume, long-term survival, and cytokine secretion were assessed. In addition, the toxicity of each treatment on liver and kidneys was examined. Our results indicated that the relative tumor volume significantly increased in the mice receiving intratumoral TGFaL3-SEB (p < 0.05). Surprisingly, 5 out of the 14 mice were cleared from the tumor thoroughly in 10-25 days after intratumoral administration of TGFaL3-SEB. Quantification of cytokines clearly showed that the mice receiving intratumoral SEB significantly secreted higher interferon gamma (IFN-gamma) and tumor necrosis factor alpha (TNF-alpha) compared with the other groups (p < 0.05). The antitumor effect was followed by inhibition of cell proliferation (Ki-67) and micro vascularization (CD31). The highest and lowest levels of tumor necrosis were observed in the intratumoral administration of TGF alpha L3-SEB (85 ) and PBS (14 ), respectively. Intratumoral injection of TGF alpha L3-SEB increased the lifespan of the mice so 37.5 of them could survive for more than 6 months (p < 0.05). Overall, our findings indicated that intratumoral administration of TGF alpha L3-SEB effectively inhibited the growth of breast tumors through induction of necrosis and suppressing proliferation and angiogenesis without systemic toxicity.