ERBB3 mutations in cancer: biological aspects, prevalence and therapeutics

被引:83
|
作者
Kiavue, Nicolas [1 ]
Cabel, Luc [1 ,2 ]
Melaabi, Samia [1 ]
Bataillon, Guillaume [1 ]
Callens, Celine [1 ]
Lerebours, Florence [1 ]
Pierga, Jean-Yves [1 ,3 ]
Bidard, Francois-Clement [1 ,2 ]
机构
[1] PSL Res Univ, Inst Curie, Dept Med Oncol, Paris, France
[2] Versailles St Quentin en Yvelines Univ, Paris Saclay Univ, Paris, France
[3] Paris Descartes Univ, Paris, France
关键词
GROWTH-FACTOR RECEPTOR; TYROSINE KINASE INHIBITOR; CELL LUNG-CANCER; GENOMIC CHARACTERIZATION; BREAST; ACTIVATION; DOMAIN; TUMOR; HER3; LANDSCAPE;
D O I
10.1038/s41388-019-1001-5
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
HER3, a member of the EGFR family of receptor tyrosine kinases coded by the ERBB3 gene, plays an important role in cancer, despite its lack of intrinsic kinase activity. As with genes coding for potential heterodimeric partners of HER3, EGFR, and HER2, oncogenic mutations of ERBB3 have been explored by several studies. In this review, we discuss the evidence presenting ERBB3 somatic mutations as potential tumoral drivers. We then show that ERBB3 mutations are not uncommon in many cancer types. Finally, we present the recent results of several studies evaluating different therapeutic approaches for treating patients with oncogenic ERBB3 mutations.
引用
收藏
页码:487 / 502
页数:16
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