西妥昔单抗
表皮生长因子受体
头颈部鳞状细胞癌
顺铂
癌症研究
表皮生长因子受体抑制剂
医学
癌变
表皮生长因子
头颈部癌
生长因子受体
肿瘤科
癌症
内科学
受体
化疗
结直肠癌
作者
Ines De Pauw,An Wouters,Jolien Van den Bossche,Vanessa Deschoolmeester,Hasan Baysal,Patrick Pauwels,Marc Peeters,Jan B. Vermorken,Filip Lardon
出处
期刊:Cancer Biotherapy and Radiopharmaceuticals
[Mary Ann Liebert]
日期:2017-09-01
卷期号:32 (7): 229-238
被引量:14
标识
DOI:10.1089/cbr.2017.2216
摘要
Aberrant signaling of the epidermal growth factor receptor (EGFR) plays a crucial role in the tumorigenesis of many cancer types, including head and neck squamous cell carcinoma (HNSCC), making it a compelling drug target. After initial promising results of EGFR-targeted therapies such as cetuximab, the problem of therapeutic resistance is emerging and new treatment options are necessary. In contrast to first-generation EGFR inhibitors, MEHD7945A (duligotuzumab) is a monoclonal antibody with dual EGFR/HER3 specificity. Consequently, treatment with MEHD7945A may result in a more pronounced therapeutic benefit. In this study, sensitivity to MEHD7945A as a single agent and in combination with cisplatin was investigated in cetuximab-sensitive and -resistant HNSCC cell lines under normal and reduced oxygen conditions. The results demonstrated that sensitivity to MEHD7945A was cell line dependent and influenced by oxygen concentration. An additive, but not synergistic, interaction between MEHD7945A and cisplatin was observed. In conclusion, MEHD7945A has the potential to partially overcome cetuximab resistance. Nevertheless, further research is warranted to determine additional resistance mechanisms to cetuximab treatment besides HER3 signaling. Unraveling these mechanisms will ultimately lead to the development of new therapeutic strategies to improve the response to EGFR blockage.
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