1 Center for Oncological Research (CORE), University of Antwerp , Antwerp, Belgium .
2 Department of Pathology, Antwerp University Hospital , Antwerp, Belgium .
Cancer Biother Radiopharm. 2017 Sep;32(7):229-238.
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.
表皮生长因子受体 (EGFR) 的异常信号在许多癌症类型的肿瘤发生中起着至关重要的作用,包括头颈部鳞状细胞癌 (HNSCC),使其成为一个引人注目的药物靶点。在西妥昔单抗等 EGFR 靶向治疗最初取得有希望的结果后,治疗耐药性的问题正在出现,需要新的治疗选择。与第一代 EGFR 抑制剂不同,MEHD7945A(度鲁妥珠单抗)是一种具有双重 EGFR/HER3 特异性的单克隆抗体。因此,使用 MEHD7945A 治疗可能会带来更显著的治疗益处。在这项研究中,在正常和低氧条件下,研究了 MEHD7945A 作为单一药物以及与顺铂联合治疗对西妥昔单抗敏感和耐药的 HNSCC 细胞系的敏感性。结果表明,对 MEHD7945A 的敏感性取决于细胞系,并受氧浓度的影响。观察到 MEHD7945A 和顺铂之间存在相加而非协同的相互作用。总之,MEHD7945A 有可能部分克服西妥昔单抗耐药性。然而,需要进一步的研究来确定除 HER3 信号以外的西妥昔单抗治疗的其他耐药机制。揭示这些机制最终将导致开发新的治疗策略来改善对 EGFR 阻断的反应。