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薄荷醇对人癌细胞活力的影响。

Effect of litreol on the viability of human cancer cells.

作者信息

Russo Alessandra, Cardile Venera, De Ioannes Alfredo, Garbarino Juan

机构信息

Department of Biological Chemistry, Medical Chemistry and Molecular Biology, University of Catania, V.le A. Doria 6, 95125 Catania, Italy.

出版信息

Chem Biol Interact. 2009 May 15;179(2-3):178-84. doi: 10.1016/j.cbi.2008.10.013. Epub 2008 Oct 19.

Abstract

Members of the family Anacardiaceae are known to contain a number of biologically active substances, such as phenolic lipids, alkyl-catechols and alkyl-resorcinols. In the present study, human cancer cell lines, DU-145 cells (androgen-insensitive prostate cancer cells), KB cells (human epidermoid cells), and human melanoma cell line, M14, were treated for 72 h with 0.59-9.5 microM litreol (3-[pentadecyl-10-enyl-catechol]), a alkyl-catechol isolated from Lithraea caustica (Molina) Hook. & Arn. The results showed, for the first time, that litreol inhibited cancer cell viability in a dose-dependent manner. In addition, the treatment with this compound at 0.59-1.18 microM concentrations induced apoptotic cell death, demonstrated by the fragmentation of genomic DNA and by a significant increase of caspase-3 activity. The significant production of reactive oxygen species (ROS) evidenced in these experimental conditions could trigger the apoptosis cascades. Taken together, these results demonstrate that litreol attenuate the growth of human cancer cells, at least in part, triggering an apoptotic process, and they may offer a further impulse to the development of its analogues with more potent efficacy against human cancer cells.

摘要

漆树科植物已知含有多种生物活性物质,如酚类脂质、烷基儿茶酚和烷基间苯二酚。在本研究中,人癌细胞系DU-145细胞(雄激素不敏感前列腺癌细胞)、KB细胞(人表皮样细胞)和人黑色素瘤细胞系M14,用0.59 - 9.5微摩尔/升的litreol(3 - [十五烷基-10-烯基儿茶酚])处理72小时,litreol是从Lithraea caustica (Molina) Hook. & Arn.中分离得到的一种烷基儿茶酚。结果首次表明,litreol以剂量依赖的方式抑制癌细胞活力。此外,在0.59 - 1.18微摩尔浓度下用该化合物处理可诱导凋亡性细胞死亡,这通过基因组DNA的片段化和caspase-3活性的显著增加得以证明。在这些实验条件下所证实的活性氧(ROS)的大量产生可能触发凋亡级联反应。综上所述,这些结果表明litreol至少部分地通过触发凋亡过程来减弱人癌细胞的生长,并且它们可能为开发对人癌细胞具有更强效力的类似物提供进一步的推动。

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