TY - JOUR
T1 - Fibroblast growth factor receptor-1 as a potential therapeutic target in sinonasal cancer
AU - Schröck, Andreas
AU - Göke, Friederike
AU - Wagner, Patrick
AU - Bode, Maike
AU - Franzen, Alina
AU - Huss, Sebastian
AU - Agaimy, Abbas
AU - Ihrler, Stephan
AU - Kirsten, Robert
AU - Kristiansen, Glen
AU - Bootz, Friedrich
AU - Lengerke, Claudia
AU - Perner, Sven
N1 - Copyright:
Copyright 2014 Elsevier B.V., All rights reserved.
PY - 2014/9
Y1 - 2014/9
N2 - Despite multimodal treatment, sinonasal malignancies have an unfavorable prognosis. The purpose of this study was to elucidate if these tumors harbor amplifications of the fibroblast growth factor receptor 1 (FGFR1) gene, which has recently been identified as a potential therapeutic target in squamous cell lung cancer. Methods. One hundred twelve primary tumors (including squamous cell carcinoma [SCC], carcinoma associated with an inverted papilloma, sinonasal undifferentiated carcinoma [SNUC], adenocarcinoma, adenoid cystic carcinoma [ACC], esthesioneuroblastoma, and 9 corresponding lymph node metastases) were assessed by fluorescence in situ hybridization (FISH) for FGFR1 copy number status. Human papillomavirus (HPV) status was assessed by p16 immunohistochemical as a surrogate marker. Results. FGFR1 amplification was found in subsets of sinonasal SCCs (20%), carcinomas associated with an inverted papilloma (33%), and SNUCs (5%). In all cases, metastatic tumor samples shared the same FGFR1 amplification status as the corresponding primary tumor tissue. None of the FGFR1-amplified tumors expressed p16. Conclusion. FGFR1 amplification represents a potential molecular target in a subset of patients with sinonasal cancer.
AB - Despite multimodal treatment, sinonasal malignancies have an unfavorable prognosis. The purpose of this study was to elucidate if these tumors harbor amplifications of the fibroblast growth factor receptor 1 (FGFR1) gene, which has recently been identified as a potential therapeutic target in squamous cell lung cancer. Methods. One hundred twelve primary tumors (including squamous cell carcinoma [SCC], carcinoma associated with an inverted papilloma, sinonasal undifferentiated carcinoma [SNUC], adenocarcinoma, adenoid cystic carcinoma [ACC], esthesioneuroblastoma, and 9 corresponding lymph node metastases) were assessed by fluorescence in situ hybridization (FISH) for FGFR1 copy number status. Human papillomavirus (HPV) status was assessed by p16 immunohistochemical as a surrogate marker. Results. FGFR1 amplification was found in subsets of sinonasal SCCs (20%), carcinomas associated with an inverted papilloma (33%), and SNUCs (5%). In all cases, metastatic tumor samples shared the same FGFR1 amplification status as the corresponding primary tumor tissue. None of the FGFR1-amplified tumors expressed p16. Conclusion. FGFR1 amplification represents a potential molecular target in a subset of patients with sinonasal cancer.
UR - http://www.scopus.com/inward/record.url?scp=84906077609&partnerID=8YFLogxK
U2 - 10.1002/hed.23443
DO - 10.1002/hed.23443
M3 - Journal articles
C2 - 23913758
AN - SCOPUS:84906077609
SN - 1043-3074
VL - 36
SP - 1253
EP - 1257
JO - Head and Neck
JF - Head and Neck
IS - 9
ER -