Analyzing expression and phosphorylation of the EGF receptor in HNSCC.
Cell Line, Tumor
Cetuximab
/ pharmacology
Down-Regulation
/ drug effects
ErbB Receptors
/ metabolism
Erlotinib Hydrochloride
/ pharmacology
Gene Expression Profiling
/ methods
Gene Expression Regulation, Neoplastic
/ drug effects
Head and Neck Neoplasms
/ metabolism
Homeostasis
/ drug effects
Humans
Phosphorylation
/ drug effects
Squamous Cell Carcinoma of Head and Neck
/ metabolism
Tissue Array Analysis
Journal
Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288
Informations de publication
Date de publication:
19 09 2019
19 09 2019
Historique:
received:
11
04
2019
accepted:
24
08
2019
entrez:
21
9
2019
pubmed:
21
9
2019
medline:
27
10
2020
Statut:
epublish
Résumé
Overexpression of the epidermal growth factor receptor (EGFR) in head and neck squamous cell carcinomas (HNSCC) is considered to cause increased EGFR activity, which adds to tumorigenicity and therapy resistance. Since it is still unclear, whether EGFR expression is indeed associated with increased activity in HNSCC, we analyzed the relationship between EGFR expression and auto-phosphorylation as a surrogate marker for activity. We used a tissue micro array, fresh frozen HNSCC tumor and corresponding normal tissue samples and a large panel of HNSCC cell lines. While we observed substantial overexpression only in approximately 20% of HNSCC, we also observed strong discrepancies between EGFR protein expression and auto-phosphorylation in HNSCC cell lines as well as in tumor specimens using Western blot and SH2-profiling; for the majority of HNSCC EGFR expression therefore seems not to be correlated with EGFR auto-phosphorylation. Blocking of EGFR activity by cetuximab and erlotinib points to increased EGFR activity in samples with increased basal auto-phosphorylation. However, we could also identify cells with low basal phosphorylation but relevant EGFR activity. In summary, our data demonstrate that EGFR expression and activity are not well correlated. Therefore EGFR positivity is no reliable surrogate marker for EGFR activity, arguing the need for alternative biomarkers or functional predictive tests.
Identifiants
pubmed: 31537844
doi: 10.1038/s41598-019-49885-5
pii: 10.1038/s41598-019-49885-5
pmc: PMC6753061
doi:
Substances chimiques
Erlotinib Hydrochloride
DA87705X9K
EGFR protein, human
EC 2.7.10.1
ErbB Receptors
EC 2.7.10.1
Cetuximab
PQX0D8J21J
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
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