A role for the pseudokinase HER3 in the acquired resistance against EGFR- and HER2-directed targeted therapy

被引:23
|
作者
Claus, Jeroen [1 ]
Patel, Gargi [2 ,3 ]
Ng, Tony [2 ,3 ]
Parker, Peter J. [1 ]
机构
[1] Canc Res UK London Res Inst, London WC2A 3LY, England
[2] Kings Coll London, Richard Dimbleby Dept Canc Res, Randall Div, London SE1 1UL, England
[3] Kings Coll London, Div Canc Studies, London SE1 1UL, England
基金
英国生物技术与生命科学研究理事会; 英国医学研究理事会; 英国工程与自然科学研究理事会;
关键词
cancer; drug resistance; epidermal growth factor receptor (EGFR); human epidermal growth factor receptor 2 (HER2); human epidermal growth factor receptor 3 (HER3); kinase inhibition; CLINICAL-PRACTICE GUIDELINES; GROWTH-FACTOR RECEPTOR; CANCER CELLS; LUNG-CANCER; KINASE INHIBITORS; AXL KINASE; DIAGNOSIS; TRASTUZUMAB; ACTIVATION; ERBB3;
D O I
10.1042/BST20140043
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Specific inhibition of members of the EGFR (epidermal growth factor receptor) family, particularly EGFR and HER2 (human epidermal growth factor receptor 2), are an important therapeutic strategy in many human cancers. Compared with classical chemotherapy, these targeted therapeutics are very specific and initially effective, but acquired resistance against these targeted therapies is a recurring threat. A growing body of recent work has highlighted a pseudokinase in the EGFR family, HER3, and its ligand, NRG (neuregulin flu), to be of importance in models of resistant cancers, as well as in patients. In the present article, we describe some of the roles in which HER3 can mediate acquired resistance and discuss the current efforts to target HER3 itself in cancer.
引用
收藏
页码:831 / 836
页数:6
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