Stazione Zoologica Anton Dohrn, Istituo Nazionale di Biologia, Ecologia e Biotecnologie Marine, Villa Comunale, 80121 Naples, Italy.
Bio-Organic Chemistry Unit, Institute of Biomolecular Chemistry-CNR, Via Campi Flegrei 34, Pozzuoli, 80078 Naples, Italy.
Mar Drugs. 2018 Dec 12;16(12):502. doi: 10.3390/md16120502.
Marine dinoflagellates are a valuable source of bioactive molecules. Many species produce cytotoxic compounds and some of these compounds have also been investigated for their anticancer potential. Here, we report the first investigation of the toxic dinoflagellate as source of water-soluble compounds with antiproliferative activity against human lung cancer cells. A multi-step enrichment of the phenol⁻water extract yielded a bioactive fraction with specific antiproliferative effect (IC = 0.4 µg·mL) against the human lung adenocarcinoma cells (A549 cell line). Preliminary characterization of this material suggested the presence of glycoprotein with molecular weight above 20 kDa. Interestingly, this fraction did not exhibit any cytotoxicity against human normal lung fibroblasts (WI38). Differential gene expression analysis in A549 cancer cells suggested that the active fraction induces specific cell death, triggered by mitochondrial autophagy (mitophagy). In agreement with the cell viability results, gene expression data also showed that no mitophagic event was activated in normal cells WI38.
海洋甲藻是生物活性分子的宝贵来源。许多种甲藻产生细胞毒性化合物,其中一些化合物也因其抗癌潜力而受到研究。在这里,我们首次报道了有毒甲藻作为水溶性化合物的来源,这些化合物对人类肺癌细胞具有抗增殖活性。多步富集酚-水提取物得到了具有特异性抗增殖作用的生物活性部分(IC = 0.4 µg·mL),对人肺腺癌细胞(A549 细胞系)。对该物质的初步表征表明,存在分子量大于 20 kDa 的糖蛋白。有趣的是,该部分对人正常肺成纤维细胞(WI38)没有任何细胞毒性。A549 癌细胞中的差异基因表达分析表明,活性部分诱导由线粒体自噬(mitophagy)引发的特异性细胞死亡。与细胞活力结果一致,基因表达数据还表明,正常细胞 WI38 中未激活任何自噬事件。