Nerve Growth Factor (NGF)Receptor Survival Axis in Head and Neck Squamous Cell Carcinoma

被引：26

作者：

Dudas, Jozsef ^{[1
]}

Dietl, Wolfgang ^{[1
]}

Romani, Angela ^{[1
]}

Reinold, Susanne ^{[1
]}

Glueckert, Rudolf ^{[1
]}

Schrott-Fischer, Anneliese ^{[1
]}

Dejaco, Daniel ^{[1
]}

Chacko, Lejo Johnson ^{[1
]}

Tuertscher, Raphaela ^{[1
]}

Schartinger, Volker Hans ^{[1
]}

Riechelmann, Herbert ^{[1
]}

机构：

[1] Med Univ Innsbruck, Dept Otorhinolaryngol, Anichstr 35, A-6020 Innsbruck, Austria

来源：

INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES | 2018年 / 19卷 / 06期

关键词：

cytokeratin; necrosis; cell cycle arrest; TissueFaxs; BREAST-CANCER CELLS; NEUROTROPHIC FACTOR; FACTOR RECEPTOR; IN-VITRO; TUMOR; EXPRESSION; P75(NTR); PROSTATE; BDNF; NGF;

D O I：

10.3390/ijms19061771

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：

Neurotrophins and their receptors might regulate cell survival in head and neck squamous cell carcinoma (HNSCC). mRNA expression of nerve growth factor (NGF) and protein synthesis of high (NTRK1) and low affinity neurotrophin (p75 neurotrophin receptor; NTR) receptors were investigated in normal oral mucosa and in HNSCC. HNSCC cell lines were treated with mitomycin C (MMC) and cell survival was investigated. Normal and malignant epithelial cells expressed NGF mRNA. NTRK1 was upregulated in 80% of HNSCC tissue, and 50% of HNSCC samples were p75NTR positive. Interestingly, in HNSCC tissue: NTRK1 and p75NTR immunohistochemical reactions were mutually exclusive. Detroit 562 cell line contained only p75NTR, UPCI-SCC090 cells synthesized NTRK1 but not p75NTR and SCC-25 culture had p75NTR and NTRK1 in different cells. NGF (100 ng/mL) significantly improved (1.4-fold) the survival of cultured UPCI-SCC090 cells after MMC-induced cell cycle arrest, while Detroit 562 cells with high levels of p75NTR did not even get arrested by single short MMC treatment. p75NTR in HNSCC might be related with NGF-independent therapy resistance, while NTRK1 might transduce a survival signal of NGF and contribute in this way to improved tumor cell survival after cell cycle arrest.

引用

页数：23

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