ABX试验
表皮生长因子
表皮生长因子受体
癌症研究
表皮样癌
单克隆抗体
A431电池
生长因子受体抑制剂
医学
吉非替尼
生长因子
生长抑制
转化生长因子-α
癌症
受体
生物
细胞生长
抗体
内科学
免疫学
细胞周期
癌基因
生物化学
统计
数学
作者
David H. Lynch,Xiaodong Yang
标识
DOI:10.1053/sonc.2002.31522
摘要
Overexpression of the epidermal growth factor receptor (EGFR) has been observed in a wide variety of human cancers and is associated with a poor clinical prognosis. In many cases, growth of the tumor cells is dependent on EGFR-mediated signals, because inhibition of binding of factors to the EGFR leads to cell death. Using XenoMouse technology, a fully human EGFR-specific monoclonal antibody, ABX-EGF, with high affinity (5 x 10(-11) mol/L) has been generated. ABX-EGF blocks binding of both epidermal growth factor and transforming growth factor alpha to the EGFR, inhibits tyrosine phosphorylation of the EGFR, and inhibits cellular proliferation. In vivo, ABX-EGF not only blocks formation of human epidermoid carcinoma A431 xenografts in athymic mice, but also mediates therapeutic elimination of established tumors and acts cooperatively with chemotherapeutics in mediating tumor regression. These observations provide a strong basis for the development of ABX-EGF as a therapeutic agent for human solid tumors that overexpress EGFR.
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