| Literature DB >> 26835877 |
Bénédicte Rysman1,2, François Mouawad1,2, Abigaëlle Gros2, Amélie Lansiaux2, Dominique Chevalier1, Samuel Meignan2.
Abstract
Human epidermal growth factor receptor 3 (HER3) is a member of the human epidermal growth factor receptor (HER) family. The main characteristic of HER3 is that it does not possess tyrosine kinase activity, unlike other HERs. The role of HER3 in tumorigenesis has now been recognized, particularly in head and neck squamous cell carcinomas (HNSCCs). Despite conflicting studies, HER3 was found to be overexpressed in HNSCC samples, and correlates with disease progression and poor survival, especially when it is coexpressed with other HERs. HER3 is a significant factor in HNSCC treatment resistance. Indeed, HER3 is a major mechanism described for cetuximab resistance because of modification of epidermal growth factor receptor (EGFR) internalization and by phosphotidylinositol-3-kinase (PI3K)/AKT signaling pathway activation. HER3 also affects resistance to tyrosine kinase inhibitors (TKIs) and thereby promotes treatment escape and radiotherapy resistance by activation of the survival signaling pathway. To counteract this, pharmacologic inhibitors of HER3 are currently in development and could significantly improve HNSCC treatment.Entities:
Keywords: cetuximab; head and neck squamous cell carcinoma (HNSCC); human epidermal growth factor receptor 3 (HER3); radiotherapy; resistance; tyrosine kinase inhibitor
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Year: 2016 PMID: 26835877 DOI: 10.1002/hed.24367
Source DB: PubMed Journal: Head Neck ISSN: 1043-3074 Impact factor: 3.147