首页> 外文期刊>Journal of biomolecular screening: The official journal of the Society for Biomolecular Screening >Selective Cytotoxicity Evaluation in Anticancer Drug Screening of Fractionated Plant Extracts
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Selective Cytotoxicity Evaluation in Anticancer Drug Screening of Fractionated Plant Extracts

机译:分馏植物提取物抗癌药物筛选的选择性细胞毒性评价

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Chosen to reflect biodiversity in a phylogenetic sense, 100 fractionated plant extracts were screened in vitro for cytotoxicity following extraction and fractionation (polypeptide isolation). Of these 100 extracts, 30 were selected and then characterized preliminarily for antitumor potency and mode of action by testing them on two cell lines and primary cultures of human tumor cells. On the basis of cytotoxicity potency, 10 of the extracts were further characterized for anticancer activity in 10 human tumor cell lines. This final testing resulted in seven potential lead plants with superior evidence of antitumor potential: Colchicum autumnale L. (Colchicaceae), Digitalis lanata Ehrh. and Digitalis purpurea L. (Plantaginaceae), Helleborus cyclophyllus Boiss. (Ranunculaceae), Menyanthes trifoliata L. (Menyanthaceae), and Viola arvensis Murr. and Viola patrinii Ging. (Violaceae). Within a database of antitumor compounds, the activity profiles of the extracts from these seven plants were compared, by correlation analysis, with those of more than 100 other compounds, including 39 standard drugs from different classes of cytotoxic mechanisms. The activity profiles of six of these candidates were uncorrelated with those of the standard drugs, possibly indicating new pathways of drug-mediated cell death.
机译:为了从系统发育的角度反映生物多样性,在提取和分级分离(多肽分离)后,体外筛选了100种分级提取的植物提取物的细胞毒性。在这100种提取物中,选择了30种,然后通过在两种细胞系和人类肿瘤细胞的原代培养物中进行测试来初步表征其抗肿瘤效力和作用方式。基于细胞毒性效力,进一步表征了10种提取物在10种人类肿瘤细胞系中的抗癌活性。最终测试结果产生了七种潜在的铅植物,它们具有抗肿瘤潜力的出色证据:秋水仙(秋茄科),洋地黄。和洋地黄(Plantaginaceae),鸢尾草。 (毛un科),Menyanthes trifoliata L.(Menyanthaceae)和Viola arvensis Murr。和Viola patrinii Ging。 (堇菜科)。在抗肿瘤化合物数据库中,通过相关性分析,将这七种植物提取物的活性谱与100多种其他化合物(包括来自不同细胞毒性机制的39种标准药物)的活性谱进行了比较。这些候选物中的六个的活性谱与标准药物的活性谱不相关,可能表明药物介导的细胞死亡的新途径。

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