Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Pivot Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Target Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Query: EC:2.7.10.1 (
ERK
)
95,504
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
c-
MET
is a membrane spanning receptor tyrosine kinase for hepatocyte growth factor (HGF) also termed scatter factor. Transmitting signals from mesenchymal to epithelial cells, the HGF/c-
MET
axis mediates a range of biological processes that stimulate proliferation, motility, invasiveness, morphogenesis, apoptosis, and angiogenesis. Aberrant c-
MET
signal transduction favours tumorigenesis with the acquisition of invasive and metastatic phenotypes. Biological functions of c-
MET
may strongly vary according to microenvironmental changes, which occur at different stages of tumorigenesis and include also HGF/c-
MET
activation in stromal cells. In this review, we focused on abnormalities in non-
nasopharyngeal squamous cell carcinoma
of the head & neck. While the prevalence of c-
MET
mutations and amplifications ranges 0-25%, c-
MET
upregulation can be found in the majority of squamous head & neck carcinomas. Despite marked heterogeneity in published scoring methods, immunohistochemical overexpression of c-
MET
has been typically linked to advanced stages and associated with impaired survival and/or resistance to radiotherapy, chemoradiotherapy, and cetuximab. Experimental studies in cell lines and patient-derived xenografts using various c-
MET
antagonists (both as single-agents and in combination with cytotoxic and epidermal growth factor receptor [
EGFR
]-directed agents) yielded promising results, albeit benefit in clinical trials remains to be demonstrated. Consequently, selecting more active agents and integrating them effectively in studies, which incorporate predictive biomarkers such as c-
MET
gene mutations, amplifications, and overexpression, remains challenging. Further investigations should increase emphasis on disentangling the role of tumour-stromal interactions and analyse their potential as modifiers of drug response.
...
PMID:Understanding c-MET signalling in squamous cell carcinoma of the head & neck. 2825 94