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非洲姜中虹吸唇酮细胞毒性作用的评估:体外分析

Evaluation of cytotoxic effect of siphonochilone from African ginger: an in vitro analysis.

作者信息

Ortigosa-Palomo Alba, Fuentes-Ríos David, Quiñonero Francisco, Melguizo Consolación, Ortiz Raul, López-Romero Juan M, Prados Jose

机构信息

Institute of Biopathology and Regenerative Medicine (IBIMER), Center of Biomedical Research (CIBM), University of Granada, Granada, Spain.

Department of Anatomy and Embryology, Faculty of Medicine, University of Granada, Granada, Spain.

出版信息

Environ Toxicol. 2024 Sep;39(9):4333-4346. doi: 10.1002/tox.24308. Epub 2024 May 14.

Abstract

Plants provide a wide array of compounds that can be explored for potential anticancer properties. Siphonochilone, a furanoterpene that represents one of the main components of the African plant Siphonochilus aethiopicus, shows numerous health benefits. However, to date, its antiproliferative properties have not been tested. The aim of this study was to analyze the cytotoxic effects of siphonochilone on a panel of cancer cell lines and its underlying mechanism of action. Our results demonstrated that siphonochilone exhibited significant cytotoxic effects on pancreatic, breast, lung, colon, and liver cancer cell lines showing a IC ranging from 22 to 124 μM at 72 h of treatment and highlighting its cytotoxic effect against MCF7 and PANC1 breast and pancreas cancer cell lines (22.03 and 39.03 μM, respectively). Cell death in these tumor lines was mediated by apoptosis by the mitochondrial pathway, as evidenced by siphonochilone-induced depolarization of the mitochondrial membrane potential. In addition, siphonochilone treatment involves the generation of reactive oxygen species that may contribute to apoptosis induction. In this work, we described for the first time the cytotoxic properties of siphonochilone and provided data about the molecular processes of cell death. Although future studies will be necessary, our results support the interest in this molecule in relation to their clinical application in cancer, and especially in breast and pancreatic cancer.

摘要

植物提供了大量具有潜在抗癌特性的化合物可供探索。西波诺奇隆是一种呋喃萜类化合物,是非洲植物埃塞俄比亚西波诺奇唇兰的主要成分之一,具有多种健康益处。然而,迄今为止,其抗增殖特性尚未得到测试。本研究的目的是分析西波诺奇隆对一组癌细胞系的细胞毒性作用及其潜在作用机制。我们的结果表明,西波诺奇隆对胰腺、乳腺、肺、结肠和肝癌细胞系表现出显著的细胞毒性作用,在处理72小时时的IC范围为22至124μM,并突出了其对MCF7和PANC1乳腺癌和胰腺癌细胞系的细胞毒性作用(分别为22.03和39.03μM)。这些肿瘤细胞系中的细胞死亡是由线粒体途径介导的凋亡引起的,西波诺奇隆诱导的线粒体膜电位去极化证明了这一点。此外,西波诺奇隆处理涉及活性氧的产生,这可能有助于诱导凋亡。在这项工作中,我们首次描述了西波诺奇隆的细胞毒性特性,并提供了有关细胞死亡分子过程的数据。尽管未来还需要进一步研究,但我们的结果支持对该分子在癌症临床应用方面的研究兴趣,尤其是在乳腺癌和胰腺癌方面。

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