Uncovering the role of brain-derived neurotrophic factor/tyrosine kinase receptor B signaling in head and neck malignancies.
Juliana Kern de MoraesVivian Petersen WagnerFlávia Sirotheau Correa PontesPablo Agustin VargasCaroline Brunetto de FariasRafael RoeslerManoela Domingues MartinsPublished in: Journal of oral pathology & medicine : official publication of the International Association of Oral Pathologists and the American Academy of Oral Pathology (2017)
Brain-derived neurotrophic factor (BDNF) is a member of the neurotrophin family of growth factors that was first known as responsible for sustain the growth, function, and plasticity of neural cells. BDNF exerts its effects by binding to the tyrosine kinase receptor B (TrkB). The BDNF/TrkB axis has been reported to be overexpressed in several neurogenic and non-neurogenic tumors. Its higher expression was associated with a poor prognosis to patients affected by different human malignancies, tumor growth, invasion, and metastasis; epithelial-mesenchymal transition and resistance to chemotherapy. BDNF/TrkB represent promising targets to the development of novel anticancer therapies. Some clinical trials are currently evaluating the efficacy of Trk protein-target drugs in different types of solid tumors. To date, few groups have evaluated the DNF/TrkB pathway in head and neck malignancies. The aims of this study were to review the literature concerning the role of BDNF/TrkB activation in head and neck squamous cell carcinoma and malignant salivary gland tumors and to discuss future perspectives of BDNF/TrkB-target therapy.
Keyphrases
- tyrosine kinase
- poor prognosis
- stress induced
- epidermal growth factor receptor
- epithelial mesenchymal transition
- long non coding rna
- clinical trial
- spinal cord injury
- end stage renal disease
- binding protein
- chronic kidney disease
- ejection fraction
- systematic review
- induced apoptosis
- newly diagnosed
- stem cells
- prognostic factors
- randomized controlled trial
- squamous cell carcinoma
- oxidative stress
- radiation therapy
- mesenchymal stem cells
- transforming growth factor
- locally advanced
- rectal cancer