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南非叶球兰酮类化合物对癌细胞的细胞毒性及其诱导细胞凋亡的潜力。

Cytotoxicity of Carvotacetones from Sphaeranthus africanus Against Cancer Cells and Their Potential to Induce Apoptosis.

机构信息

Institute of Pharmaceutical Sciences, Department of Pharmacognosy, University of Graz, Austria.

Department of Pharmacognosy, School of Medicine, Vietnam National University HCM City, Ho Chi Minh City, Vietnam.

出版信息

Planta Med. 2023 May;89(6):624-636. doi: 10.1055/a-1988-2207. Epub 2023 Jan 31.

Abstract

Three carvotacetones (1 - 3: ) isolated from were screened in 60 cancer cell lines at the National Cancer Institute (NCI) within the Developmental Therapeutics Program (DTP). At the concentration of 10 M, compound 1: (3,5-diangeloyloxy-7-hydroxycarvotacetone) turned out to be the most active compound against ACHN and UO-31 renal cancer cell lines with growth percent values of - 100% (all cells dead). Compound 2: (3-angeloyloxy-5-[2″,3″-epoxy-2″-methylbutanoyloxy]-7-hydroxycarvotacetone) showed strong effects in SK-MEL-5 melanoma and ACHN renal cancer cells with inhibition values of 93% and 97%, respectively. Compound 3: (3-angeloyloxy-5-[3″-chloro-2″-hydroxy-2″-methylbutanoyloxy]-7-hydroxy-carvotacetone) exhibited a quite strong effect on renal cancer cells with a growth inhibitory effect of 96% against ACHN and UO-31 cells. When treated with five different concentrations of 1: (1 × 10, 1 × 10, 1 × 10, 1 × 10, and 1 × 10 M), HOP-92 cells were found to be most sensitive with GI, TGI, and LC values of 0.17, 0.40, and 0.96 µM, respectively. When using the ApoTox-Glo triplex assay to evaluate the apoptosis inducing effects of seven carvotacetones isolated from in CCRF-CEM cells, compounds 1:  - 6: increased caspase-3/7 activity with 1, 2: , and 4: (3-angeloyloxy-5,7-dihydroxycarvotacetone) exhibiting the highest activitiy, indicating induction of caspase-dependent apoptosis.

摘要

从 中分离得到的三种 Carvotacetones(1-3:)在国立癌症研究所(NCI)发育治疗计划(DTP)的 60 种癌细胞系中进行了筛选。在 10 μM 的浓度下,化合物 1:(3,5-二当归酰氧基-7-羟基 Carvotacetone)对 ACHN 和 UO-31 肾癌细胞系的活性最高,生长百分比值为-100%(所有细胞死亡)。化合物 2:(3-当归酰氧基-5-[2″,3″-环氧-2″-甲基丁酰氧基]-7-羟基 Carvotacetone)对 SK-MEL-5 黑色素瘤和 ACHN 肾癌细胞具有强烈的作用,抑制率分别为 93%和 97%。化合物 3:(3-当归酰氧基-5-[3″-氯-2″-羟基-2″-甲基丁酰氧基]-7-羟基-carvotacetone)对肾癌细胞具有相当强的作用,对 ACHN 和 UO-31 细胞的生长抑制作用为 96%。当用五种不同浓度的 1:(1×10、1×10、1×10、1×10 和 1×10 M)处理 HOP-92 细胞时,发现细胞对 GI、TGI 和 LC 值最敏感,分别为 0.17、0.40 和 0.96 μM。当使用 ApoTox-Glo 三联体测定法评估从 中分离得到的七种 Carvotacetones 在 CCRF-CEM 细胞中诱导细胞凋亡的效果时,化合物 1:-6:增加了 caspase-3/7 的活性,其中 1、2:和 4:(3-当归酰氧基-5,7-二羟基 Carvotacetone)表现出最高的活性,表明诱导了 caspase 依赖性细胞凋亡。

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