LAQV-REQUIMTE, Department of Chemistry, University of Aveiro, 3810-193 Aveiro, Portugal.
REQUIMTE/LAQV, Department of Chemistry and Biochemistry, Faculty of Sciences, University of Porto, 4169-007 Porto, Portugal.
Int J Mol Sci. 2021 Jul 16;22(14):7604. doi: 10.3390/ijms22147604.
Seaweeds are one of the largest producers of biomass in the marine environment and a source of multiple bioactive metabolites with valuable health benefits. Among these, phlorotannins have been widely recognized for their promising bioactive properties. The potential antitumor capacity of -derived phlorotannins remains, however, poorly explored, especially in gastrointestinal tract-related tumors. Therefore, this work aimed to evaluate the cytotoxic properties and possible mechanisms by which crude extract (CRD), phlorotannin-rich extract (EtOAc), and further phlorotannin-purified fractions (F1-F9) trigger cell death on different tumor cell lines of the gastrointestinal tract, using flow cytometry. The results indicate that samples exert specific cytotoxicity against tumor cell lines without affecting the viability of normal cells. Moreover, it was found that, among the nine different phlorotannin fractions tested, F5 was the most active against both Caco-2 colorectal and MKN-28 gastric cancer cells, inducing death via activation of both apoptosis and necrosis. The UHPLC-MS analysis of this fraction revealed, among others, the presence of a compound tentatively identified as eckstolonol and another as fucofurodiphlorethol, which could be mainly responsible for the promising cytotoxic effects observed in this sample. Overall, the results herein reported contribute to a better understanding of the mechanisms behind the antitumor properties of phlorotannin-rich extracts.
海藻是海洋环境中最大的生物量生产者之一,也是多种具有重要健康益处的生物活性代谢物的来源。其中,岩藻多酚因其有希望的生物活性特性而被广泛认可。然而,来源于 的岩藻多酚的潜在抗肿瘤能力在胃肠道相关肿瘤中仍未得到充分探索。因此,本研究旨在通过流式细胞术评估 粗提取物(CRD)、富含岩藻多酚的提取物(EtOAc)以及进一步的岩藻多酚纯化馏分(F1-F9)对不同胃肠道肿瘤细胞系的细胞毒性特性和可能的作用机制。结果表明, 样品对肿瘤细胞系具有特异性细胞毒性,而不影响正常细胞的活力。此外,发现在测试的 9 种不同的岩藻多酚馏分中,F5 对 Caco-2 结肠直肠癌细胞和 MKN-28 胃癌细胞最具活性,通过激活凋亡和坏死诱导细胞死亡。该馏分的 UHPLC-MS 分析表明,其中存在一种化合物,暂定名为 Eckstolonol,另一种为 Fucofurodiphlorethol,它们可能是该样品中观察到的有希望的细胞毒性作用的主要原因。总体而言,本研究结果有助于更好地理解富含岩藻多酚的提取物抗肿瘤特性背后的机制。