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- W2355200265 abstract "Objective Mouse factor Ⅶ(mfⅦ), ligand of tissue factor (TF)which is frequently overexpressed during neovascularlzation activated bv tumor growth, was fused to staphylococcus enterotoxin A (SEA) that mediates greater intensity of T-cell activation against tumor cells. The anti-tumor effects of the mfⅦ-SEA chimeric protein were evaluated. Methods Fusion of SEA and mfⅦ cDNA was constructed using adenovirus vector and produced in 293 packaging cell lines. The 293 cells containing the adenovirus were administered subcutaneously to mice. Fluorescence studies at the injection site and the liver were performed 3 days later. Mouse prostatic tumor RM-1 cells and mouse sarcoma MCA 205 H12 cell lines were then used in mice to create lung metastasis and subcutaneous tumor to carry out efficacy evaluation, respectively. Results Adenovirus released from the injected 293 cells only infected the subcutaneous tissue at the injection site. The in vivo experiments in mice revealed that formation of lung metastasis was strongly inhibited by the mfⅦ-SEA (23 ±8 ) compared to the vacant vector control group( 193±38) and PBS control group(211±42) ( P 〈 0.01 ). The mfⅦ-SEA also strongly suppressed tumor growth at the subcutaneous injection site (342.6 ±107.1 ) mm^3 compared to that of vacant vector control (2244.3±350) mm^3 and SEA (1208.3±210) mm^3 by the 23rd day. Conclusion The chimeric protein mfⅦ-SEA significantly inhibits lung metastasis formation and local tumor growth.Key words: Factor Ⅶ; Staphylococcus enterotoxin A; Neoplasm growth; Neoplasm metastasis" @default.
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- W2355200265 date "2005-08-01" @default.
- W2355200265 modified "2023-09-25" @default.
- W2355200265 title "Anti-tumor effects of mouse factor VII-staphylococcus enterotoxin A (mfVII) chimeric protein in mice" @default.
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