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Anti-EGFR antibody cetuximab is secreted by oral squamous cell carcinoma and alters EGF-driven mesenchymal transition

机译:抗EGFR抗体西妥昔单抗由口腔鳞状细胞癌分泌,改变EGF驱动的间充质转换

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摘要

Genetic amplification, overexpression, and increased signaling from the epidermal growth factor receptor (EGFR) are often found in oral squamous cell carcinoma (OSCC) and thus EGFR is frequently targeted molecularly by the therapeutic antibody cetuximab. We assessed effects of cetuximab in control of EGF-driven malignant traits of OSCC cells. EGF stimulation promoted progression level of mesenchymal traits in OSCC cells, which were attenuated by cetuximab but incompletely. We pursued a potential mechanism underlying such incomplete attenuation of OSCC malignant traits. Cetuximab promoted secretion of EGFR-EVs by OSCC cells and failed to inhibit EGF-driven secretion of EGFR-EVs. Cetuximab was also found to be robustly secreted with the EGFR-EVs by the OSCC cells. Thus, EGF promotes the level of mesenchymal traits of OSCC cells and secretion of EGFR-EVs, which involve cetuximab resistance.
机译:从表皮生长因子受体(EGFR)中的遗传扩增,过表达和增加的信号传导通常在口腔鳞状细胞癌(OSCC)中发现,因此EGFR经常通过治疗性抗体香司昔单抗靶向。 我们评估了西汀昔单抗控制EAGF驱动的OSCC细胞恶性性状的影响。 EGF刺激促进了OSCC细胞中间充质性的渐近性状的进展水平,其被Cetuximab衰减但不完全。 我们追求了潜在的机制,潜在的机制,对OSCC恶性特征的这种不完全衰减。 西妥昔单抗通过OSCC细胞促进EGFR-EVS的分泌,并未抑制EGFR-EV的EGF驱动的分泌。 还发现西妥昔单抗用OSCC细胞用EGFR-EVS鲁布布地分泌。 因此,EGF促进OSCC细胞的间充质性和EGFR-EV的分泌的水平,其涉及西妥昔单抗抗性。

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