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抗癌药物对亚汇合及汇合后多层培养物的细胞毒性作用。

Cytotoxic effects of anticancer agents on subconfluent and multilayered postconfluent cultures.

作者信息

Pizao P E, Peters G J, Van Ark-Otte J, Smets L A, Smitskamp-Wilms E, Winograd B, Pinedo H M, Giaccone G

机构信息

Department of Oncology, Free University Hospital, Amsterdam, The Netherlands.

出版信息

Eur J Cancer. 1993;29A(11):1566-73. doi: 10.1016/0959-8049(93)90296-r.

Abstract

The cytotoxic effects of conventional (doxorubicin, 5-fluorouracil, cisplatin) and investigational (2',2'-difluorodeoxycytidine, hexadecylphosphocholine, EO9, rhizoxin) anticancer drugs were studied in subconfluent and multilayered postconfluent cultures of human colon and ovarian carcinoma cell lines. Chemosensitivity was assessed 4 days after a 24-h drug exposure with the sulphorhodamine B assay. Except for rhizoxin, all drugs tested yielded an EC50 (drug concentration producing absorbance readings 50% lower than those of non-treated wells) in postconfluent cultures that were higher than an EC50 obtained with subconfluent cultures. Compared with subconfluent cultures, postconfluent cultures showed decreased cellular nucleotide concentrations and ATP/ADP ratios, in addition to an increased percentage of G0/G1 cells. The activity of DT-diaphorase, a reductase involved in the bioactivation of EO9, was similar in sub- and postconfluent cultures. These results indicate similarity of the postconfluent model presented with those obtained with in vivo models and more complex in vitro techniques.

摘要

在人结肠和卵巢癌细胞系的亚汇合及多层汇合后培养物中研究了传统抗癌药物(阿霉素、5-氟尿嘧啶、顺铂)和试验性抗癌药物(2',2'-二氟脱氧胞苷、十六烷基磷胆碱、EO9、根霉素)的细胞毒性作用。在24小时药物暴露4天后,用磺酰罗丹明B试验评估化学敏感性。除根霉素外,所有测试药物在汇合后培养物中产生的半数有效浓度(EC50,即产生的吸光度读数比未处理孔低50%的药物浓度)均高于在亚汇合培养物中获得的EC50。与亚汇合培养物相比,汇合后培养物显示细胞核苷酸浓度和ATP/ADP比值降低,此外G0/G1期细胞百分比增加。参与EO9生物活化的还原酶DT-黄递酶的活性在亚汇合和汇合后培养物中相似。这些结果表明,所呈现的汇合后模型与体内模型和更复杂的体外技术所获得的模型相似。

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