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具有间接抗肿瘤活性机制的药物筛选的体外方法:黄酮乙酸的呫吨酮类似物

In vitro methods for screening agents with an indirect mechanism of antitumour activity: xanthenone analogues of flavone acetic acid.

作者信息

Ching L M, Finlay G J, Joseph W R, Baguley B C

机构信息

Cancer Research Laboratory, Auckland University School of Medicine, New Zealand.

出版信息

Eur J Cancer. 1991;27(12):1684-9. doi: 10.1016/0277-5379(91)90446-k.

Abstract

Xanthenone-4-acetic acid (XAA) resembles flavone acetic acid (FAA) in its effects on solid tumours in mice. The activity of methyl-substituted XAA derivatives in vitro was determined using 18 h 51Cr-release assays, continuous exposure growth inhibition assays and stimulation of tumouricidal activity of cultured murine resident peritoneal macrophages. The macrophage assay identified the high biological activity and dose potency of 5-MeXAA in vivo, and was the most accurate in vitro predictor of the ability of congeners to induce either haemorrhagic necrosis of subcutaneous Lewis lung and colon 38 tumours or splenic natural killer activity. In vitro immune stimulation may be more appropriate than direct cytotoxicity for screening compounds with indirect mechanisms of antitumour activity.

摘要

呫吨酮-4-乙酸(XAA)在对小鼠实体瘤的作用方面类似于黄酮乙酸(FAA)。使用18小时51Cr释放试验、连续暴露生长抑制试验以及对培养的小鼠驻留腹膜巨噬细胞的杀肿瘤活性刺激来测定甲基取代的XAA衍生物的体外活性。巨噬细胞试验确定了5-MeXAA在体内的高生物活性和剂量效力,并且是同源物诱导皮下Lewis肺癌和结肠38肿瘤出血性坏死或脾自然杀伤活性能力的最准确体外预测指标。对于筛选具有间接抗肿瘤活性机制的化合物,体外免疫刺激可能比直接细胞毒性更合适。

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