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首页> 外文期刊>Journal of Cancer Research and Clinical Oncology >Additive cytotoxic effect of cisplatin and X-irradiation on human glioma cell cultures derived from biopsy-tissue.
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Additive cytotoxic effect of cisplatin and X-irradiation on human glioma cell cultures derived from biopsy-tissue.

机译:顺铂和X射线对源自活检组织的人神经胶质瘤细胞培养物的附加细胞毒性作用。

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PURPOSE: Investigation of the in vitro cytotoxic effect of X-rays, either alone or combined with cisplatin on early passage cell cultures derived from human glioblastoma multiforme biopsy tissue. MATERIALS AND METHODS: Fresh tumour specimens from four patients were processed to cell cultures. The U373 glioma cell line was used as a reference. Early passage cell cultures were X-irradiated (0-8 Gy) either alone or in combination with cisplatin (0.5-1 microgram/ml). Cell survival was determined by either clonogenic assay or the colorimetric MTT assay. Survival curves were generated and mathematically analysed using the linear quadratic model, to obtain the radiosensitivity parameters alpha, beta, and SF2, i.e., the Surviving Fraction after 2 Gy. RESULTS: Two patient-derived glioma cell cultures and the U373 cell line showed rather high SF2 values of 0.61-0.72 in the clonogenic assay, indicating relative high radiation resistance. Cisplatin alone (1 microgram/ml) reduced cell survival by 10-30% (n = 4). When combined with irradiation, a clear additive cytotoxic effect of cisplatin was demonstrated by the unaltered value of the alpha-parameter for reproductive cell death. CONCLUSION: Cisplatin exerted an additive rather than radiosensitising cytotoxic effect in uncharacterised patient derived glioma cell cultures.
机译:目的:研究X射线单独或与顺铂联合使用对人胶质母细胞瘤多形活检组织早期传代细胞培养的体外细胞毒性作用。材料与方法:将来自四名患者的新鲜肿瘤标本进行细胞培养。将U373神经胶质瘤细胞系用作参考。单独或与顺铂(0.5-1微克/毫升)一起对早期传代的细胞培养物进行X射线照射(0-8 Gy)。细胞存活通过克隆形成测定或比色MTT测定来确定。生成生存曲线,并使用线性二次模型进行数学分析,以获得放射敏感性参数α,β和SF2,即2 Gy后的生存分数。结果:两种源自患者的神经胶质瘤细胞培养物和U373细胞系在克隆形成试验中均显示出较高的SF2值0.61-0.72,表明相对较高的抗辐射性。单独使用顺铂(1微克/毫升)可使细胞存活率降低10-30%(n = 4)。当与放射线结合使用时,通过生殖细胞死亡的α参数的不变值证明了顺铂具有明显的累加细胞毒性作用。结论:顺铂在未鉴定的患者来源的神经胶质瘤细胞培养物中发挥加性作用而不是放射增敏作用。

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