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首页> 外文期刊>Journal of Cancer Research and Clinical Oncology >Concurrent use of vinorelbine and gefitinib induces supra-additive effect in head and neck squamous cell carcinoma cell lines.
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Concurrent use of vinorelbine and gefitinib induces supra-additive effect in head and neck squamous cell carcinoma cell lines.

机译:长春瑞滨和吉非替尼的同时使用可在头颈部鳞状细胞癌细胞系中诱导超加性作用。

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PURPOSE: Squamous cell carcinoma of the head and neck (HNSCC) remains a clinical challenge because of the high rate of locoregional disease recurrence. Standard treatment includes surgery, radiation, chemoradiation or a combination of these approaches. New therapies are needed to achieve improved survival, quality of life and organ function in these patients. A novel molecular targeted therapy incorporated into our current treatment strategies may have a significant role in the treatment of HNSCC. The aim of this study was to evaluate the sensitivity of HNSCC cell lines to vinorelbine combined with gefitinib in vitro. METHODS: Six recently established cell lines were used: UT-SCC-9, -11, -19A, -29 and -34 (laryngeal SCC) and UT-SCC-33 (oral cavity SCC). Chemosensitivity was tested using the 96-well plate clonogenic assay. The vinorelbine concentrations used varied between 0.4 and 1.0 nM and the gefitinib concentrations varied between 0.05 and 1.6 muM. Survival data were fitted to the LQ model, and the area under the curve (AUC) value was obtained with numerical integration. The type of interaction was determined by comparing the AUC ratio of the two drugs to the survival fraction (SF) of gefitinib alone. RESULTS: In the current study the combination of vinorelbine and gefitinib had a clear supra-additive or additive cytotoxic effect on the HNSCC cell lines. CONCLUSIONS: This finding is encouraging as a proof of the possible benefit of combing an EGFR targeting compound with a cell cycle specific drug and warrants further studies of available combinations in vitro.
机译:目的:由于局部区域疾病复发率高,头颈部鳞状细胞癌(HNSCC)仍然是临床挑战。标准治疗包括手术,放射线,化学放射线或这些方法的组合。需要新的疗法来提高这些患者的生存率,生活质量和器官功能。纳入我们当前治疗策略的新型分子靶向治疗可能在HNSCC的治疗中起重要作用。这项研究的目的是评估HNSCC细胞系对长春瑞滨联合吉非替尼联合治疗的敏感性。方法:使用了六种最近建立的细胞系:UT-SCC-9,-11,-19A,-29和-34(喉SCC)和UT-SCC-33(口腔SCC)。使用96孔平板克隆形成试验测试化学敏感性。所使用的长春瑞滨浓度在0.4至1.0 nM之间变化,吉非替尼浓度在0.05至1.6μM之间变化。将生存数据拟合到LQ模型,并通过数值积分获得曲线下面积(AUC)值。通过比较两种药物的AUC比值与吉非替尼单独的生存率(SF)来确定相互作用的类型。结果:在目前的研究中,长春瑞滨和吉非替尼的组合对HNSCC细胞系具有明显的超加性或加性细胞毒性作用。结论:这一发现令人鼓舞,证明了将EGFR靶向化合物与细胞周期特异性药物结合可能产生的益处,并值得进一步研究体外可用组合。

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