Department of Biotechnology and Biosciences, University of Milano Bicocca, Piazza della Scienza 2, 20126 Milano, Italy.
Department of Earth and Environmental Sciences DISAT, University of Milano Bicocca, Piazza della Scienza 1, 20126 Milano, Italy.
Mar Drugs. 2022 Feb 11;20(2):134. doi: 10.3390/md20020134.
The octocoral family Alcyoniidae represents a rich source of bioactive substances with intriguing and unique structural features. This review aims to provide an updated overview of the compounds isolated from Alcyoniidae and displaying potential cytotoxic activity. In order to allow a better comparison among the bioactive compounds, we focused on molecules evaluated in vitro by using the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl-2H-tetrazolium bromide (MTT) assay, by far the most widely used method to analyze cell proliferation and viability. Specifically, we surveyed the last thirty years of research, finding 153 papers reporting on 344 compounds with proven cytotoxicity. The data were organized in tables to provide a ranking of the most active compounds, to be exploited for the selection of the most promising candidates for further screening and pre-clinical evaluation as anti-cancer agents. Specifically, we found that (22,24)-24-methyl-22,25-epoxyfurost-5-ene-3β,20β-diol (), 3β,11-dihydroxy-24-methylene-9,11-secocholestan-5-en-9-one (), (24)-ergostane-3β,5α,6β,25 tetraol (), sinulerectadione (), sinulerectol C (), and cladieunicellin I () exhibited stronger cytotoxicity than their respective positive control and that their mechanism of action has not yet been further investigated.
柳珊瑚科代表了具有有趣和独特结构特征的生物活性物质的丰富来源。本综述旨在提供柳珊瑚科中分离出的具有潜在细胞毒性的化合物的最新概述。为了能够更好地比较生物活性化合物,我们专注于通过使用 3-(4,5-二甲基噻唑-2-基)-2,5-二苯基-2H-四唑溴盐(MTT)测定法在体外评估的分子,该方法是迄今为止分析细胞增殖和活力最广泛使用的方法。具体来说,我们调查了过去三十年的研究,发现有 153 篇论文报道了 344 种具有证明的细胞毒性的化合物。这些数据被组织成表格,以提供最活跃的化合物的排名,以便从这些化合物中选择最有前途的候选物,用于进一步的筛选和临床前评估作为抗癌剂。具体而言,我们发现 (22,24)-24-甲基-22,25-环氧呋甾-5-烯-3β,20β-二醇 (), 3β,11-二羟基-24-亚甲基-9,11-去甲胆甾烷-5-烯-9-酮 (), (24)-麦角甾烷-3β,5α,6β,25-四醇 (), sinulerectadione (), sinulerectol C (), 和 cladieunicellin I () 的细胞毒性比各自的阳性对照更强,其作用机制尚未进一步研究。