The effect of antibody against vascular endothelial growth factor on tumorgrowth and metastasis

Citation
Gq. Wang et al., The effect of antibody against vascular endothelial growth factor on tumorgrowth and metastasis, J CANC RES, 124(11), 1998, pp. 615-620
Citations number
17
Categorie Soggetti
Onconogenesis & Cancer Research
Journal title
JOURNAL OF CANCER RESEARCH AND CLINICAL ONCOLOGY
ISSN journal
01715216 → ACNP
Volume
124
Issue
11
Year of publication
1998
Pages
615 - 620
Database
ISI
SICI code
0171-5216(199811)124:11<615:TEOAAV>2.0.ZU;2-T
Abstract
Vascular endothelial growth factor (VEGF), a very important in the process of tumor angiogenesis, was chosen as a target in a study to determine wheth er manipulation of angiogenesis with antibody against VEGF may interrupt tu mor growth and metastasis. Anti-VEGF antibody was obtained from immunized r abbits, purified on an affinity column, and identified as neutralized antib ody by Mile's assay. IVTA(2)MA891, a murine spontaneous breast cancer with a high rate of metastasis in lung in TA(2) x 615 F1 mice, was chosen as an animal model in this study, because of the high expression of VEGF in the p rimary tumor as well as in the lung metastatic tumor. The anti-VEGF antibod y could inhibit growth of S180 sarcoma in a dose-dependent manner, and the inhibition rate could reach 41.0% with a dose of 200 mu g mouse(-1) day(-1) . Anti-VEGF antibody could inhibit tumor growth by 76.2% in nude mice beari ng human gastric cancer (MGC 803). When anti-VEGF antibody was combined wit h I-131-3H11, a murine monoclonal antibody conjugated with I-131, only one of five nude mice developed tumor and 84.0% more inhibition of tumor growth was obtained in comparison with treatment by I-131-3H11 alone. The growth of the primary tumor was inhibited by 44.0% and the number and size of the metastatic foci in the lungs were reduced by 73.0% and 83.7% respectively i n the animal model, with a high rate of metastasis in lung. The anti-VEGF a ntibody may be potentially useful for clinical treatment of cancer and meta stasis.