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Combination of phosphotidylinositol‐3‐kinase targeting with cetuximab and irradiation: A preclinical study on an orthotopic xenograft model of head and neck cancer
Author(s) -
Bozec Alexandre,
Ebran Nathalie,
Radosevic–Robin Nina,
Chamorey Emmanuel,
Yahia Hedi Ben,
Marcie Serge,
Gautier Mathieu,
Penault–Llorca Frédérique,
Milano Gérard
Publication year - 2017
Publication title -
head and neck
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.012
H-Index - 127
eISSN - 1097-0347
pISSN - 1043-3074
DOI - 10.1002/hed.24560
Subject(s) - cetuximab , medicine , head and neck squamous cell carcinoma , pi3k/akt/mtor pathway , epidermal growth factor receptor , mapk/erk pathway , cancer research , protein kinase b , kinase , egfr inhibitors , head and neck cancer , cancer , oncology , colorectal cancer , signal transduction , biology , biochemistry , microbiology and biotechnology
Background The purpose of this study was to investigate the effects of combining the phosphotidylinositol‐3‐kinase (PI3K) inhibitor buparlisib (BKM)120 with the anti‐epidermal growth factor receptor (EGFR) agent cetuximab and radiotherapy (RT) on an orthotopic model of head and neck squamous cell carcinoma (HNSCC). Methods We evaluated the antitumor efficacy of BKM120, cetuximab, and RT, administered alone or in combination, using the human PIK3CA‐mutated HNSCC cell line, CAL33, injected into the floor of the mouth of nude mice. Results Compared with control, the BKM120‐cetuximab and the BKM120‐cetuximab‐RT combinations led to the highest tumor inhibition ( p < .001). The highest inhibitory effect of treatments on cell proliferation, mitogen‐activated protein kinase (MAPK) and PI3K/protein kinase B (AKT)/mammalian target of rapamycin (mTOR) signaling pathways were found with the BKM120‐cetuximab association. The association of BKM120 and cetuximab with RT inhibited RT‐induced activation of the MAPK pathway. Conclusion These results can serve as a preclinical rationale for innovative treatments combining PI3K inhibition with anti‐EGFR therapies and irradiation in patients with HNSCC. © 2016 Wiley Periodicals, Inc. Head Neck 39: 151–159, 2017