Effects of culture method on response to EGFR therapy in head and neck squamous cell carcinoma cells

被引:33
作者
Ayuso, Jose M. [1 ,2 ,3 ]
Vitek, Ross [2 ,3 ]
Swick, Adam D. [4 ]
Skala, Melissa C. [1 ,2 ,3 ]
Wisinski, Kari B. [3 ]
Kimple, Randall J. [3 ,4 ]
Lambert, Paul F. [6 ]
Beebe, David J. [2 ,3 ,5 ]
机构
[1] Morgridge Inst Res, 330N Orchard St, Madison, WI USA
[2] Univ Wisconsin, Dept Biomed Engn, Madison, WI 53706 USA
[3] Univ Wisconsin, Carbone Canc Ctr, Madison, WI 53706 USA
[4] Univ Wisconsin, Dept Human Oncol, Madison, WI USA
[5] Univ Wisconsin, Dept Pathol & Lab Med, Madison, WI 53706 USA
[6] Univ Wisconsin, Sch Med & Publ Hlth, Dept Oncol, Madison, WI USA
关键词
CETUXIMAB RESISTANCE; CANCER-CELLS;
D O I
10.1038/s41598-019-48764-3
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The EGFR pathway plays a critical role in head and neck squamous cell carcinoma (HNSCC). Targeted therapies against the EGFR are utilized as a treatment for HNSCCC. However, patient response is heterogeneous and molecular biomarkers are lacking to predict patient response. Therefore, functional assays where drug response is directly evaluated in tumor cells are an interesting alternative. Previous studies have shown that experimental conditions modify the drug response observed in functional assays. Thus, in this work the influence of the culture environment on response to Cetuximab (EGFR monoclonal antibody) and AZD8055 (mTOR inhibitor) was evaluated. HNSCC UM-SCC-1 and UM-SCC-47 cells were cultured in 2D monoculture and compared with: 2D co-culture with cancer-associated fibroblasts (CAF); 3D culture in collagen hydrogels; and 3D culture in tumor spheroids. The results showed UM-SCC-1 drug response significantly changed in the different culture environments; leading to an increase in drug resistance in the CAF co-culture and the 3D spheroids. Conversely, UM-SCC-47 exhibited a more constant drug response across culture conditions. In conclusion, this work highlights the importance of culture conditions that modulate response to EGFR pathway inhibition.
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页数:9
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