Emerging therapies in gastrointestinal cancers

被引:19
|
作者
Nautiyal, Jyoti
Rishi, Arun K.
Majumdar, Adhip P. N.
机构
[1] Wayne State Univ, Dept Internal Med, Detroit, MI 48201 USA
[2] Vet Affairs Med Ctr, Dept Internal Med, Karmanos Canc Inst, Detroit, MI 48201 USA
关键词
gastrointestinal cancers; carcinogenesis; targeted therapies; Pan-ErbB family; EGF-receptor related protein;
D O I
10.3748/wjg.v12.i46.7440
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Members of the receptor tyrosine kinase family, that include EGFR, ErbB-2/HER-2, ErbB-3/HER-3 and ErbB-4/ HER-4, are frequently implicated in experimental models of epithelial cell neoplasia as well as in human cancers. Therefore, interference with the activation of these growth factor receptors represents a promising strategy for development of novel and selective anticancer therapies. Indeed, a number of inhibitors that target either EGFR or HER-2, with the exception of a few that target both; have been developed for treatment of epithelial cancers. Since most solid tumors express different ErbB receptors and/or their ligands, identification of inhibitor(s), targeting multiple EGFR family members may provide a therapeutic benefit to a broader patient population. Here we describe the significance of an ErbB family of receptors in epithelial cancers, and summarize different available therapeutics targeting these receptors. It also emphasizes the need to develop pan-ErbB inhibitors and discusses EGF-Receptor Related Protein, a recently isolated negative regulator of EGFR as a potential pan-ErbB therapeutic for a wide variety of epithelial cancers. (c) 2006 The WJG Press. All rights reserved.
引用
收藏
页码:7440 / 7450
页数:11
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