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体外研究中长春瑞滨与放疗联合用于头颈部鳞状细胞癌的情况

Concomitant vinorelbine and radiation in head and neck squamous cell carcinoma in vitro.

作者信息

Erjala Kaisa, Pulkkinen Jaakko, Kulmala Jarmo, Grénman Reidar

机构信息

Department of Otorhinolaryngology-Head and Neck Surgery, Turku University Central Hospital, Turku, Finland.

出版信息

Acta Oncol. 2004;43(2):169-74. doi: 10.1080/02841860310023110.

Abstract

Concomitant chemoradiotherapy has been used for locally advanced head and neck squamous cell carcinoma (HNSCC) particularily with cisplatin, 5-FU, methotrexate, bleomycin and taxanes. Vinorelbine is a semisynthetic vinca alcaloid, which causes a block in the G2/M phase of the cell cycle. HNSCC cell lines have previously been reported to be sensitive to vinorelbine in nanomolar concentrations. In the current study the effect of vinorelbine as a radiosensitizer in vitro was studied and eight recently established head and neck SCC cell lines of the UT-SCC-series were tested. Vinorelbine concentrations of 0.4-1.6 nM were used, corresponding to the IC70, IC50 and IC30 values of each cell line, resulting in 30%, 50% and 70% inhibition in clonogenic survival. The desired concentrations of vinorelbine were added to the medium and the cells were plated in 96-well culture plates in this solution. The plated cells were irradiated 24 h later with 4MeV photons generated by a linear accelerator and incubated at 37 degrees C with 5% CO2 for 4 weeks. Thereafter, the number of wells containing coherent, living colonies, consisting of 32 cells or more, was counted. The plating efficiency was calculated and the fraction survival data were fitted to the linear quadratic model [F = exp[-(alphaD + betaD2)]]. An additive effect of combining vinorelbine and irradiation could be demonstrated. The dose-dependent decrease in survival was seen at vinorelbine doses of 0.4-1.6 nM in all cell lines tested.

摘要

同步放化疗已用于局部晚期头颈部鳞状细胞癌(HNSCC),特别是与顺铂、5-氟尿嘧啶、甲氨蝶呤、博来霉素和紫杉烷联合使用。长春瑞滨是一种半合成长春花生物碱,可导致细胞周期的G2/M期阻滞。此前有报道称HNSCC细胞系对纳摩尔浓度的长春瑞滨敏感。在本研究中,研究了长春瑞滨作为体外放射增敏剂的作用,并测试了UT-SCC系列最近建立的8种头颈部鳞状细胞癌细胞系。使用的长春瑞滨浓度为0.4-1.6 nM,对应于每个细胞系的IC70、IC50和IC30值,导致克隆形成存活率分别抑制30%、50%和70%。将所需浓度的长春瑞滨添加到培养基中,然后将细胞接种在该溶液的96孔培养板中。接种24小时后用直线加速器产生的4MeV光子照射细胞,并在37℃、5%二氧化碳条件下孵育4周。此后,对含有由32个或更多细胞组成的连贯活菌落的孔数进行计数。计算接种效率,并将存活分数数据拟合到线性二次模型[F = exp[-(αD + βD2)]]。可以证明长春瑞滨与放疗联合具有相加作用。在所有测试的细胞系中,长春瑞滨剂量为0.4-1.6 nM时均可见存活剂量依赖性降低。

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