安非雷古林
表皮生长因子受体
生物
卵巢癌
表皮生长因子
癌症研究
神经调节蛋白
癌症
皮调节素
单克隆抗体
抗体
生长因子
免疫学
内科学
受体
肿瘤科
医学
生物化学
遗传学
作者
Sílvia Carvalho,Moshit Lindzen,Mattia Lauriola,Niloofar Shirazi,Sudarson Sekhar Sinha,A Abdul-Hai,Keren Levanon,Jacob Korach,Iris Barshack,Yaël C. Cohen,Amir Onn,Gordon B. Mills,Yosef Yarden
出处
期刊:Oncogene
[Springer Nature]
日期:2015-04-27
卷期号:35 (4): 438-447
被引量:45
摘要
Growth factors of the epidermal growth factor (EGF)/neuregulin family are involved in tumor progression and, accordingly, antibodies that intercept a cognate receptor, epidermal growth factor receptor (EGFR)/ERBB1, or a co-receptor, HER2, have been approved for cancer therapy. Although they might improve safety and delay onset of chemoresistance, no anti-ligand antibodies have been clinically approved. To identify suitable ligands, we surveyed fluids from ovarian and lung cancer patients and found that amphiregulin (AREG) is the most abundant and generalized ligand secreted by advanced tumors. AREG is a low affinity EGFR ligand, which is upregulated following treatment with chemotherapeutic drugs. Because AREG depletion retarded growth of xenografted ovarian tumors in mice, we generated a neutralizing monoclonal anti-AREG antibody. The antibody inhibited growth of ovarian cancer xenografts and strongly enhanced chemotherapy efficacy. Taken together, these results raise the possibility that AREG and other low- or high-affinity binders of EGFR might serve as potential targets for cancer therapy.
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