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Dual mAb HER family blockade in head and neck cancer human cell lines combined with photon therapy

机译:结合光子疗法在头颈癌人类细胞系中双重 mAb HER家族阻断

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摘要

Head and neck cancer stem cells (CSCs) are highly resistant to treatment. When EGFR is overexpressed in head and neck squamous cell carcinoma (HNSCC), HER2 and HER3 are also expressed. The aim of the present study was to investigate the effect of HER1/2/3 blockade through a combination of cetuximab and pertuzumab, with or without photon irradiation, on the proliferation and migration/invasion capabilities of an HNSCC chemo- and radioresistant human cell line (SQ20B) and its corresponding stem cell subpopulation. Cell proliferation, migration and invasion were studied after treatment with cetuximab +/− pertuzumab +/− 10 Gy photon irradiation. EGFR, phospho-EGFR, HER2 and HER3 protein expression levels were studied. Activation or inhibition of the RAS/MAPK and AKT-mTOR downstream signalling cascades was investigated through phospho-AKT and phospho-MEK1/2 expression. Cetuximab strongly inhibited SQ20B and FaDu cell proliferation, migration and invasion, whereas it had little effect on SQ20B-CSCs. Cetuximab–pertuzumab combined with radiation significantly inhibited SQ20B and FaDu cell and SQ20B-CSC proliferation, migration and invasion. Cetuximab–pertuzumab with 10 Gy photon irradiation switched off both phospho-AKT and phospho-MEK1/2 expression in the three populations. The triple therapy is therefore thought to inhibit SQ20B cells, SQ20B-CSCs and FaDu cells through an AKT-mTOR and Ras-MAPK downstream signalling blockade.
机译:头颈癌干细胞(CSC)对治疗具有高度抵抗力。当EGFR在头颈部鳞状细胞癌(HNSCC)中过表达时,HER2和HER3也被表达。本研究的目的是研究通过西妥昔单抗和帕妥珠单抗联合使用或不使用光子辐照对HERS / 2/3的阻断对HNSCC耐药化学和放射人类细胞增殖和迁移/侵袭能力的影响(SQ20B)及其相应的干细胞亚群。用西妥昔单抗+/- Pertuzumab +/- 10 Gy光子照射后,研究了细胞的增殖,迁移和侵袭。研究了EGFR,磷酸化EGFR,HER2和HER3蛋白的表达水平。通过磷酸化AKT和磷酸化MEK1 / 2表达研究了RAS / MAPK和AKT-mTOR下游信号级联反应的激活或抑制。西妥昔单抗强烈抑制SQ20B和FaDu细胞的增殖,迁移和侵袭,而对SQ20B-CSC几乎没有影响。西妥昔单抗-帕妥珠单抗联合放射治疗可显着抑制SQ20B和FaDu细胞以及SQ20B-CSC的增殖,迁移和侵袭。用10uxGy光子照射的西妥昔单抗-帕妥珠单抗在这三个种群中均关闭了磷酸化AKT和磷酸化MEK1 / 2的表达。因此,认为三联疗法通过AKT-mTOR和Ras-MAPK下游信号传导阻滞抑制SQ20B细胞,SQ20B-CSCs和FaDu细胞。

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