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醚脂类似物与DNA相互作用剂组合对人肿瘤细胞的体外抗增殖活性。

In vitro antiproliferative activity of combinations of ether lipid analogues and DNA-interactive agents against human tumor cells.

作者信息

Noseda A, Berens M E, White J G, Modest E J

机构信息

Department of Biochemistry, Bowman Gray School of Medicine, Wake Forest University, Winston-Salem, North Carolina 27103.

出版信息

Cancer Res. 1988 Apr 1;48(7):1788-91.

PMID:3349458
Abstract

Ether lipid analogues of platelet-activating factor (1-octadecyl-2-acetyl-sn-glycero-3-phosphocholine) possess a wide range of biological activities, including inhibition of neoplastic cell growth in vitro and in vivo. This activity is believed to be membrane mediated. Three different ether lipid analogues, 1-octadecyl-2-methyl-rac-glycero-3-phosphocholine, 1-thiohexadecyl-2-ethyl-rac-glycero-3-phosphocholine, and 4-amino-methyl-1-[2,3-(di-n-decyloxy)-n-propyl]-4-phenylpiperidine , were combined with three DNA-interactive drugs, Adriamycin, 4-hydroperoxycyclophosphamide, and cisplatin, in the expectation that combinations of drugs with different mechanisms of action might show enhanced antitumor activity. The in vitro antiproliferative activity of the combinations was measured with a semisoft agarose clonogenic assay of an ovarian adenocarcinoma cell line. Various permutations of drug combinations were studied. Isobologram analyses and different treatment schedules were performed. Enhanced antiproliferative activity was found with combinations of ether lipids with DNA-interactive drugs in comparison with single agents. Statistical evaluation of the data indicated that the increase in activity was due to an additivity phenomenon. Neither synergism nor antagonism was found.

摘要

血小板激活因子(1-十八烷基-2-乙酰基-sn-甘油-3-磷酸胆碱)的醚脂类似物具有广泛的生物活性,包括在体外和体内抑制肿瘤细胞生长。这种活性被认为是由膜介导的。三种不同的醚脂类似物,1-十八烷基-2-甲基-rac-甘油-3-磷酸胆碱、1-硫代十六烷基-2-乙基-rac-甘油-3-磷酸胆碱和4-氨基甲基-1-[2,3-(二正癸氧基)-正丙基]-4-苯基哌啶,与三种DNA相互作用药物阿霉素、4-氢过氧环磷酰胺和顺铂联合使用,期望不同作用机制的药物组合可能显示出增强的抗肿瘤活性。用卵巢腺癌细胞系的半软琼脂糖克隆形成试验测定组合药物的体外抗增殖活性。研究了药物组合的各种排列方式。进行了等效线图分析和不同的治疗方案。与单一药物相比,醚脂与DNA相互作用药物的组合具有增强的抗增殖活性。数据的统计评估表明,活性的增加是由于相加现象。未发现协同作用或拮抗作用。

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