| Literature DB >> 21461946 |
Feng-Jen Tseng1, Yen-Ku Liu, Yo-Shong Chung, Yu-Ling Lin, Chia-Hung Chen, Wan-Yi Wang, Yu-Cheng Chen, Nu-Man Tsai, Tian-Lu Cheng, Ru-Yu Pan, Tsung-Ming Hu, Ru-Ping Lee, Kuang-Wen Liao.
Abstract
Vascular endothelial growth factor (VEGF) promotes the growth of solid tumor mainly via VEGF receptor-1 and receptor-2, which are expressed preferentially in proliferating endothelial cells. Therefore, a strategy for simultaneous blockage of both VEGF receptors may have a useful therapeutic effect in tumor growth. In this study, we utilized a fusion protein which is composed of receptor binding domain of VEGF-A (RBDV) and the constant region fragment (Fc) of a human immunoglobulin G1 (IgG1), to interfere with the growth of human umbilical vein endothelial cells (HUVECs) via VEGF receptors. The results showed that RBDV-IgG1 Fc was able to bind with both VEGF receptor-1 and receptor-2. In addition, RBDV-IgG1 Fc could decrease VEGF-induced proliferation and tube formation among HUVECs. Moreover, the cytotoxic test showed RBDV-IgG1 Fc could also enhance the cytotoxic activity of human natural killing cells. The data are suggesting that the fusion protein, RBDV-IgG1 Fc, may have potential as an angiogenesis antagonist for future tumor therapy.Entities:
Year: 2011 PMID: 21461946 PMCID: PMC3081053 DOI: 10.1007/s10616-011-9340-2
Source DB: PubMed Journal: Cytotechnology ISSN: 0920-9069 Impact factor: 2.058