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地塞米松是否会抑制西妥昔单抗在头颈部鳞状细胞癌细胞系中的抗癌活性?

Does dexamethasone inhibit anticancer activity of cetuximab in squamous cell carcinoma cell lines of the head and neck?

作者信息

Wagenblast Jens, Baghi Mehran, Mörtel Susanne, Hirth Daniel, Thron Laura, Arnoldner Christoph, Gstöttner Wolfgang, May Angelika, Hambek Markus

机构信息

ENT Department, Goethe University Medical School, Frankfurt am Main, Germany.

出版信息

Oncol Rep. 2009 Jul;22(1):171-6. doi: 10.3892/or_00000421.

Abstract

Glucocorticoids such as dexamethasone are widely used as comedication in the treatment of head and neck cancer, e.g., to improve appetite and decrease weight loss and fatigue in patients with advanced disease or as antiallergic and antiemetic prophylaxis during anti-EGFR therapy. However, the literature suggests that dexamethasone induces resistance to antineoplastic agents in many solid tumor models in vitro and in vivo. Since this phenomenon has never been investigated in head and neck cancer, the present study was conducted to investigate the effect of dexamethasone on the antiproliferative activity of cetuximab in vitro in squamous cell carcinoma of the head and neck (SCCHN) cell lines. The antiproliferative effect of the anti-EGFR agent cetuximab alone and in combination with increasing concentrations of dexamethasone was examined in eight SCCHN cell lines at three different time-points (24, 48 and 72 h). Cell growth inhibition and viability were measured quantitatively using WST and LDH assays. Absolute tumor cell numbers were determined by cell counting in a Rosenthal chamber. Cetuximab alone inhibited the growth of all eight SCCHN cell lines significantly (p=0.008). In some cases the addition of dexamethasone reduced the antiproliferative activity of cetuximab (p<or=0.038) but remained significant in all of the eight SCCHN cell lines compared with untreated controls (p<or=0.028) at each drug concentration and each time-point. In contrast to the results reported for other tumor models, in our study dexamethasone showed in the majority of the evaluated dexamethasone drug concentrations and time-points no inhibition of the cytotoxic activity of cetuximab. The reasons for these discrepant findings are unclear but may be related to the degree of tumor cell differentiation or proliferation rate. Thus, further studies are required to elucidate the molecular mechanisms underlying the interaction between dexamethasone and cetuximab in different tumors.

摘要

地塞米松等糖皮质激素在头颈癌治疗中被广泛用作辅助用药,例如用于改善晚期患者的食欲、减轻体重减轻和疲劳,或在抗表皮生长因子受体(EGFR)治疗期间作为抗过敏和止吐预防用药。然而,文献表明,地塞米松在许多实体瘤体外和体内模型中会诱导产生对抗肿瘤药物的耐药性。由于这一现象从未在头颈癌中进行过研究,因此本研究旨在调查地塞米松对西妥昔单抗在体外对头颈鳞状细胞癌(SCCHN)细胞系的抗增殖活性的影响。在8种SCCHN细胞系中,于3个不同时间点(24、48和72小时)检测了抗EGFR药物西妥昔单抗单独使用以及与浓度递增的地塞米松联合使用时的抗增殖作用。使用WST和LDH检测法定量测定细胞生长抑制和活力。通过在罗森塔尔计数室中进行细胞计数来确定绝对肿瘤细胞数量。单独使用西妥昔单抗可显著抑制所有8种SCCHN细胞系的生长(p = 0.008)。在某些情况下,添加地塞米松会降低西妥昔单抗的抗增殖活性(p≤0.038),但在每个药物浓度和每个时间点,与未处理的对照相比,在所有8种SCCHN细胞系中仍具有显著差异(p≤0.028)。与其他肿瘤模型报道的结果相反,在我们的研究中,在大多数评估的地塞米松药物浓度和时间点,地塞米松并未抑制西妥昔单抗的细胞毒性活性。这些差异结果的原因尚不清楚,但可能与肿瘤细胞分化程度或增殖速率有关。因此,需要进一步研究以阐明地塞米松与西妥昔单抗在不同肿瘤中相互作用的分子机制。

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