Novel anticancer targets: revisiting ERBB2 and discovering ERBB3

被引:906
作者
Baselga, Jose [1 ]
Swain, Sandra M. [2 ]
机构
[1] Vall Hebron Univ Hosp, Vall Hebron Inst Oncol, Barcelona 08035, Spain
[2] Washington Hosp Ctr, Washington Canc Inst, Washington, DC 20010 USA
关键词
EPIDERMAL-GROWTH-FACTOR; HUMAN-BREAST-CANCER; C-ERBB-3 PROTEIN EXPRESSION; TYROSINE KINASE INHIBITOR; FACTOR RECEPTOR; MONOCLONAL-ANTIBODY; LUNG-CANCER; PHASE-II; PHOSPHATIDYLINOSITOL; 3-KINASE; DIMERIZATION INHIBITOR;
D O I
10.1038/nrc2656
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Aberrant receptor expression or functioning of the epidermal growth factor receptor (Erbb) family plays a crucial part in the development and evolution of cancer. Inhibiting the signalling activity of individual receptors in this family has advanced the treatment of a range of human cancers. In this Review we re-evaluate the role of two important family members, ERBB2 (also known as HER2) and ERBB3 (also known as HER3), and explore the mechanisms of action and preclinical and clinical data for new therapies that target signalling through these pivotal receptors. These new therapies include tyrosine kinase inhibitors, antibody-chemotherapy conjugates, heat-shock protein inhibitors and antibodies that interfere with the formation of ERBB2-ERBB3 dimers.
引用
收藏
页码:463 / 475
页数:13
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