Distribution and function of EGFR in human tissue and the effect of EGFR tyrosine kinase inhibition

被引:3
作者
Yano, S
Kondo, K
Yamaguchi, M
Richmond, G
Hutchison, M
Wakeling, A
Averbuch, S
Wadsworth, P
机构
[1] AstraZeneca KK, Kita Ku, Osaka 5310076, Japan
[2] AstraZeneca, Alderley Pk, Cheshire, England
[3] AstraZeneca, Wilmington, DE USA
关键词
EGFR; normal tissue; EGFR-TKI; gefitinib; 'Iressa';
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
From immunohistochemical and ligand-binding studies, it is known that the epidermal growth factor receptor (EGFR), a member of the erbB family of receptors, is expressed in tissues of epithelial, mesenchymal and neuronal origin and plays a major role in normal cellular processes such as proliferation., differentiation and development. EGFR is highly expressed in a number of solid tumours and its expression correlates with tumour progression, resistance to chemotherapy and a poor prognosis; it is consequently an attractive target for the rational design of novel anticancer agents. Knowledge of the role of EGFR in normal tissues will help the understanding of the adverse events associated with such agents. Studies in knockout mice and preclinical toxicology studies have shown that the major effects of inhibiting the EGFR are skin and. gastrointestinal toxicities. Clinical studies with inhibitors of EGFR, such as gefitinib, cetuximab and erlotinib, have shown a favourable adverse-event profile. primarily consisting of skin and gastrointestinal toxicities, as predicted from the mechanism-based effects observed in preclinical studies.
引用
收藏
页码:3639 / 3650
页数:12
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