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根据生长曲线和存活数据确定作为多细胞球体生长的不同人类肿瘤细胞系的放射敏感性。

Radiosensitivity of different human tumor cells lines grown as multicellular spheroids determined from growth curves and survival data.

作者信息

Schwachöfer J H, Crooijmans R P, van Gasteren J J, Hoogenhout J, Jerusalem C R, Kal H B, Theeuwes A G

机构信息

Dept. of Radiotherapy, University of Nijmegen, The Netherlands.

出版信息

Int J Radiat Oncol Biol Phys. 1989 Nov;17(5):1015-20. doi: 10.1016/0360-3016(89)90149-1.

Abstract

Five human tumor cell lines were grown as multicellular tumor spheroids (MTS) to determine whether multicellular tumor spheroids derived from different types of tumors would show tumor-type dependent differences in response to single-dose irradiation, and whether these differences paralleled clinical behavior. Multicellular tumor spheroids of two neuroblastoma, one lung adenocarcinoma, one melanoma, and a squamous cell carcinoma of the oral tongue, were studied in terms of growth delay, calculated cell survival, and spheroid control dose50 (SCD50). Growth delay and cell survival analysis for the tumor cell lines showed sensitivities that correlated well with clinical behavior of the tumor types of origin. Similar to other studies on melanoma multicellular tumor spheroids our spheroid control dose50 results for the melanoma cell line deviated from the general pattern of sensitivity. This might be due to the location of surviving cells, which prohibits proliferation of surviving cells and hence growth of melanoma multicellular tumor spheroids. This study demonstrates that radiosensitivity of human tumor cell lines can be evaluated in terms of growth delay, calculated cell survival, and spheroid control dose50 when grown as multicellular tumor spheroids. The sensitivity established from these evaluations parallels clinical behavior, thus offering a unique tool for the in vitro analysis of human tumor radiosensitivity.

摘要

培养了五种人类肿瘤细胞系作为多细胞肿瘤球体(MTS),以确定源自不同类型肿瘤的多细胞肿瘤球体在单剂量照射反应中是否会表现出肿瘤类型依赖性差异,以及这些差异是否与临床行为平行。研究了两种神经母细胞瘤、一种肺腺癌、一种黑色素瘤和一种口腔舌鳞状细胞癌的多细胞肿瘤球体的生长延迟、计算的细胞存活率和球体控制剂量50(SCD50)。肿瘤细胞系的生长延迟和细胞存活分析显示出的敏感性与起源肿瘤类型的临床行为密切相关。与其他关于黑色素瘤多细胞肿瘤球体的研究相似,我们黑色素瘤细胞系的球体控制剂量50结果偏离了一般的敏感性模式。这可能是由于存活细胞的位置,这阻止了存活细胞的增殖,从而抑制了黑色素瘤多细胞肿瘤球体的生长。这项研究表明,当作为多细胞肿瘤球体生长时,可以根据生长延迟、计算的细胞存活率和球体控制剂量50来评估人类肿瘤细胞系的放射敏感性。从这些评估中确定的敏感性与临床行为平行,从而为体外分析人类肿瘤放射敏感性提供了一个独特的工具。

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