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使用P388白血病细胞的体外肿瘤干细胞检测与体内抗肿瘤活性之间的关系。

Relationship between in vitro tumor stem cell assay and in vivo antitumor activity using the P388 leukemia.

作者信息

Marsh J C, Shoemaker R H, Salmon S E, Kern D H, Venditti J M

机构信息

Developmental Therapeutics Program, National Cancer Institute, Bethesda, Maryland.

出版信息

Int J Cell Cloning. 1988 Jan;6(1):60-8. doi: 10.1002/stem.5530060107.

Abstract

The relationship between in vitro tumor stem cell sensitivity and in vivo antitumor efficacy using 13 active antineoplastic agents was examined by means of the intraperitoneal P388 mouse leukemia system. The doses, which produced a 50% increase in life span after one, five and nine days of treatment, were all significantly correlated with the in vitro concentration producing a 70% reduction in colony formation during a seven-day continuous drug exposure. The five-day correlation was the best, followed by nine days and one day. Correlations were not improved by corrections for either in vitro drug stability or toxicity (LD50). The highly significant correlations observed in this simple retrospective analysis provide a basis for the development of more sophisticated models for the prediction of in vivo results from in vitro data.

摘要

利用腹腔注射P388小鼠白血病系统,研究了13种活性抗肿瘤药物的体外肿瘤干细胞敏感性与体内抗肿瘤疗效之间的关系。在治疗1天、5天和9天后使寿命延长50%的剂量,均与在7天持续药物暴露期间使集落形成减少70%的体外浓度显著相关。5天的相关性最佳,其次是9天和1天。对体外药物稳定性或毒性(LD50)进行校正后,相关性并未改善。在这项简单的回顾性分析中观察到的高度显著相关性,为开发更复杂的模型以根据体外数据预测体内结果提供了基础。

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