Centre of Marine Sciences, University of Algarve, Faculty of Sciences and Technology, Ed. 7, Campus of Gambelas, Faro, Portugal.
Institute of Environmental, Chemical and Pharmaceutical Sciences, Federal University of Sao Paulo, 09972-270, Sao Paulo, Brazil.
Phytomedicine. 2016 May 15;23(5):550-7. doi: 10.1016/j.phymed.2016.02.008. Epub 2016 Feb 26.
Brown macroalgae have attracted attention because they display a wide range of biological activities, including antitumoral properties. Inthis study we isolated isololiolide from Cystoseira tamariscifolia for the first time.
To examine the therapeutical potential of isololiolide against tumor cell lines.
METHODS/STUDY DESIGN: The structure of the compound was established and confirmed by 1D and 2D NMR as well as HRMS spectral analysis. The in vitro cytotoxicity was analyzed by colorimetric 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay in tumoral as well as in non-tumoral cell lines. Cell cycle arrest and induction of apoptosis were assessed by flow cytometry. Alteration of expression levels in proteins important in the apoptotic cascade was analyzed by western blotting.
Isololiolidewas isolated for the first time from the brown macroalga C.tamariscifolia. Isololiolide exhibited significant cytotoxic activity against three human tumoral cell lines, namely hepatocarcinoma HepG2 cells, whereas no cytotoxicity was found in non-malignant MRC-5 and HFF-1 human fibroblasts. Isololiolide completely disrupted the HepG2 normal cell cycle and induced significant apoptosis. Moreover, western blot analysis showed that isololiolide altered the expression of proteins that are important in the apoptotic cascade, increasing PARP cleavage and p53 expression while decreasing procaspase-3 and Bcl-2 levels.
Isololiolide isolated from C. tamariscifolia is able to exert a selective cytotoxic activity on hepatocarcinoma HepG2 cells as well as induce apoptosis through the modulation of apoptosis-related proteins.
棕色海藻因其具有广泛的生物活性而受到关注,包括抗肿瘤特性。在本研究中,我们首次从马尾藻属中分离出异柳醇内酯。
研究异柳醇内酯对肿瘤细胞系的治疗潜力。
方法/研究设计:通过 1D 和 2D NMR 以及高分辨率质谱分析确定化合物的结构。通过比色 3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四唑溴盐测定法在肿瘤和非肿瘤细胞系中分析体外细胞毒性。通过流式细胞术评估细胞周期停滞和细胞凋亡的诱导。通过蛋白质印迹分析分析在凋亡级联中起重要作用的蛋白质的表达水平变化。
首次从棕色海藻马尾藻属中分离出异柳醇内酯。异柳醇内酯对三种人肿瘤细胞系(肝癌 HepG2 细胞)表现出显著的细胞毒性活性,而在非恶性 MRC-5 和 HFF-1 人成纤维细胞中未发现细胞毒性。异柳醇内酯完全破坏 HepG2 正常细胞周期并诱导显著凋亡。此外,蛋白质印迹分析表明,异柳醇内酯改变了在凋亡级联中起重要作用的蛋白质的表达,增加了 PARP 切割和 p53 表达,同时降低了 procaspase-3 和 Bcl-2 水平。
从马尾藻属中分离出的异柳醇内酯能够对肝癌 HepG2 细胞发挥选择性细胞毒性作用,并通过调节凋亡相关蛋白诱导细胞凋亡。