Efficacy of Cetuximab and 4-PBA Combination Therapy in Human Oral Squamous Cell Carcinoma Cells

A. Noguchi, T. Nishida, Hideki Hatta, Kohji Takagi, Toshiko Kakiuchi, Shinichi Tanaka, Takashi Minamisaka, T. Nakajima, J. Imura
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引用次数: 1

Abstract

Background: Cetuximab is a powerful anti-neoplastic agent that can inhibit cell growth in oral squamous cell carcinomas (OSCCs). Unfortunately, there are cases with unfavorable outcomes. Because few studies have focused on the combined effects of cetuximab and histone deacetylase (HDAC) inhibitors, we aimed to evaluate the antitumor effect of cetuximab in combination with HDAC inhibitors in human OSCC cell lines, and investigate the mechanism of apoptosis enhancing activity thereof.Methods: We used human OSCC cell lines treated with cetuximab (500 mg/ml) and several HDAC inhibitors. The WST assay and ApoToxGlo™ Triplex Assay determined cell survival. We employed the TdT-mediated dUTP-biotin nick end labeling method to detect apoptosis. We used western blotting to examine the histone acetylation status, ER stress markers, and epidermal growth factor receptor (EGFR) signaling pathways.Results: Cetuximab in combination with 4-phenyl butyric acid (4-PBA) remarkably decreases cell growth in vitro. In addition, the combined treatment resulted in increased EGFR mRNA expression, and it promoted the activation of ERK. The combination treatment induced apoptosis at a significantly higher frequency than did either agent alone.Conclusions: The combination of cetuximab and 4-PBA is more effective against human OSCC cells than either agent alone, suggesting a potential clinical applicability of combination treatment in OSCC therapies.
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西妥昔单抗联合4-PBA治疗人口腔鳞状细胞癌的疗效观察
背景:西妥昔单抗是一种强大的抗肿瘤药物,可抑制口腔鳞状细胞癌(OSCCs)的细胞生长。不幸的是,有些情况的结果是不利的。由于很少有研究关注西妥昔单抗和组蛋白脱乙酰酶(HDAC)抑制剂的联合作用,我们旨在评估西妥昔mab与HDAC抑制剂联合在人OSCC细胞系中的抗肿瘤作用,并研究其增强细胞凋亡活性的机制。方法:我们使用用西妥昔单抗(500mg/ml)和几种HDAC抑制剂处理的人OSCC细胞系。WST检测和ApoToxGlo™ 三重法测定细胞存活率。我们采用TdT介导的dUTP生物素缺口末端标记法检测细胞凋亡。我们使用蛋白质印迹来检测组蛋白乙酰化状态、ER应激标志物和表皮生长因子受体(EGFR)信号通路。结果:西妥昔单抗与4-苯基丁酸(4-PBA)联合应用可显著降低体外细胞生长。此外,联合治疗导致EGFR mRNA表达增加,并促进ERK的激活。联合治疗诱导细胞凋亡的频率明显高于单独使用任何一种药物。结论:西妥昔单抗和4-PBA联合治疗对人OSCC细胞比单独使用任何一种药物都更有效,这表明联合治疗在OSCC治疗中具有潜在的临床适用性。
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