Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
2113944 | Cancer Letters | 2010 | 7 Pages |
Abstract
Both vascular endothelial growth factor A (VEGF) and osteopontin (OPN) can directly induce tumor angiogenesis, which is essential for the growth and metastasis of solid tumors. Here we engineered a bispecific antibody (VEGF/OPN-BsAb) using the anti-VEGF-A antibody bevacizumab and the anti-OPN antibody hu1A12. Compared with hu1A12 alone and bevacizumab alone, VEGF/OPN-BsAb was significantly more effective in inhibiting tumor angiogenesis in a highly metastatic human hepatocellular carcinoma nude mouse model. Further study demonstrated that VEGF/OPN-BsAb could effectively suppress primary tumor growth and metastasis to lungs, suggesting that it might be a promising therapeutic agent for treatment of metastatic cancer.
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Authors
Geng Kou, Jingping Shi, Lin Chen, Dapeng Zhang, Sheng Hou, Lei Zhao, Chen Fang, Lei Zheng, Xunming Zhang, Ping Liang, Xu Zhang, Bohua Li, Yajun Guo,