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Akt在获得性西妥昔单抗耐药头颈部鳞状细胞癌中的作用:一种新型联合策略的研究

The Role of Akt in Acquired Cetuximab Resistant Head and Neck Squamous Cell Carcinoma: An Study on a Novel Combination Strategy.

作者信息

Zaryouh Hannah, De Pauw Ines, Baysal Hasan, Pauwels Patrick, Peeters Marc, Vermorken Jan Baptist, Lardon Filip, Wouters An

机构信息

Center for Oncological Research (CORE), Integrated Personalized & Precision Oncology Network (IPPON), University of Antwerp, Antwerp, Belgium.

Department of Pathology, Antwerp University Hospital, Antwerp, Belgium.

出版信息

Front Oncol. 2021 Sep 10;11:697967. doi: 10.3389/fonc.2021.697967. eCollection 2021.

Abstract

The epidermal growth factor receptor (EGFR) is a therapeutic target in head and neck squamous cell carcinoma (HNSCC). Resistance to EGFR-targeted therapies, such as cetuximab, poses a challenging problem. This study aims to characterize acquired cetuximab resistance mechanisms in HNSCC cell lines by protein phosphorylation profiling. Through this, promising combination treatments can be identified to possibly overcome acquired cetuximab resistance in HNSCC. Protein phosphorylation profiling showed increased phosphorylation of Akt1/2/3 after cetuximab treatment in acquired cetuximab resistant cells compared to cetuximab sensitive cells, which was confirmed by western blotting. Based on this protein phosphorylation profile, a novel combination treatment with cetuximab and the Akt1/2/3 inhibitor MK2206 was designed. Synergy between cetuximab and MK2206 was observed in two cetuximab sensitive HNSCC cell lines and one acquired cetuximab resistant variant in simultaneous treatment schedules. In conclusion, this study demonstrates that increased Akt1/2/3 phosphorylation seems to be characteristic for acquired cetuximab resistance in HNSCC cell lines. Our results also show an additive to synergistic interaction between cetuximab and MK2206 in simultaneous treatment schedules. These data support the hypothesis that the combination of cetuximab with PI3K/Akt pathway inhibition might be a promising novel therapeutic strategy to overcome acquired cetuximab resistance in HNSCC patients.

摘要

表皮生长因子受体(EGFR)是头颈部鳞状细胞癌(HNSCC)的一个治疗靶点。对西妥昔单抗等EGFR靶向疗法产生耐药性是一个具有挑战性的问题。本研究旨在通过蛋白质磷酸化谱分析来表征HNSCC细胞系中获得性西妥昔单抗耐药机制。通过这项研究,可以确定有前景的联合治疗方案,以可能克服HNSCC中获得性西妥昔单抗耐药性。蛋白质磷酸化谱分析显示,与西妥昔单抗敏感细胞相比,获得性西妥昔单抗耐药细胞在接受西妥昔单抗治疗后Akt1/2/3的磷酸化增加,这一点通过蛋白质印迹法得到了证实。基于这种蛋白质磷酸化谱,设计了一种西妥昔单抗与Akt1/2/3抑制剂MK2206的新型联合治疗方案。在同步治疗方案中,在两种西妥昔单抗敏感的HNSCC细胞系和一种获得性西妥昔单抗耐药变体中观察到了西妥昔单抗与MK2206之间的协同作用。总之,本研究表明,Akt1/2/3磷酸化增加似乎是HNSCC细胞系中获得性西妥昔单抗耐药的特征。我们的结果还显示,在同步治疗方案中,西妥昔单抗与MK2206之间存在从相加到协同的相互作用。这些数据支持了这样一种假设,即西妥昔单抗与PI3K/Akt途径抑制的联合可能是克服HNSCC患者获得性西妥昔单抗耐药性的一种有前景的新型治疗策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0abb/8462273/eb8c9515c6b1/fonc-11-697967-g001.jpg

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