Baldini N, Scotlandi K, Serra M, Kusuzaki K, Shikita T, Manara M C, Maurici D, Campanacci M
Laboratorio di Ricerca Oncologica, Istituti Ortopedici Rizzoli, Bologna, Italy.
J Cancer Res Clin Oncol. 1992;119(2):121-6. doi: 10.1007/BF01209668.
The reliability of a simple method evaluating the pattern of subcellular binding of Adriamycin (Adriamycin binding assay, ABA) as an index of sensitivity was demonstrated in different primary cultures and in sensitive and resistant cell lines of human osteosarcoma. After exposure to Adriamycin (10 micrograms/ml for 30 min at 37 degrees C), living sensitive cells showed selective intranuclear uptake of the drug, whereas in resistant cells no distinct subcellular distribution was observed. The binding pattern of Adriamycin in sensitive and in highly resistant cells was inversely related to the expression of P-glycoprotein. However, low levels of resistance in vitro, not detectable by increased levels of expression of P-glycoprotein, were revealed by ABA. The use of ABA in combination with the estimate of P-glycoprotein expression is recommended in clinical practice as an accurate means for predicting the sensitivity of osteosarcoma to Adriamycin.
一种评估阿霉素亚细胞结合模式的简单方法(阿霉素结合试验,ABA)作为敏感性指标的可靠性,在不同的原代培养物以及人骨肉瘤的敏感和耐药细胞系中得到了证实。在暴露于阿霉素(37℃下10微克/毫升,30分钟)后,存活的敏感细胞显示出药物的选择性核内摄取,而在耐药细胞中未观察到明显的亚细胞分布。阿霉素在敏感细胞和高度耐药细胞中的结合模式与P-糖蛋白的表达呈负相关。然而,ABA揭示了体外低水平的耐药性,这通过P-糖蛋白表达水平的增加无法检测到。临床实践中建议将ABA与P-糖蛋白表达的评估结合使用,作为预测骨肉瘤对阿霉素敏感性的准确方法。