Chinese Academy of Sciences Key Laboratory of Experimental Marine Biology, Institute of Oceanology, Chinese Academy of Sciences, Qingdao 266071, China.
Department of Pharmacy, College of Chemical Engineering, Qingdao University of Science and Technology, Qingdao 266042, China.
Mar Drugs. 2019 Apr 2;17(4):207. doi: 10.3390/md17040207.
A study on the secondary metabolites of sp. XNM-4, which was derived from marine algae (Chordariaceae), led to the identification of one previously undescribed () and seventeen known compounds (2-18). Their planar structures were established by extensive spectroscopic analyses, while the stereochemical assignments were defined by electronic circular dichroism (ECD) calculations. The biological activities of the compounds were assessed on five human cancer cell lines (PANC-1, A549, MDA-MB-231, Caco-2, and SK-OV-3), and one human normal cell line (HL-7702) using an MTT [3-(4,5-dimethyl-2-thiazolyl)-2,5-diphenyl tetrazolium bromide] assay. Among them, the dimeric naphthopyrones , and exhibited potent cytotoxicity. Further mechanism studies showed that induced apoptosis, arrested the cell cycle at the G0/G1 phase in the PANC-1 cells, caused morphological changes and generated ROS; and it induces PANC-1 cells apoptosis via ROS-mediated PI3K/Akt signaling pathway.
从海洋藻类(管藻科)衍生的 sp. XNM-4 的次生代谢产物的研究,导致鉴定出一个以前未描述的()和十七个已知化合物(2-18)。通过广泛的光谱分析确定了它们的平面结构,而立体化学分配则通过电子圆二色性(ECD)计算来定义。使用 MTT [3-(4,5-二甲基-2-噻唑基)-2,5-二苯基四唑溴盐]测定法,评估了这些化合物在五种人类癌细胞系(PANC-1、A549、MDA-MB-231、Caco-2 和 SK-OV-3)和一种人类正常细胞系(HL-7702)上的生物活性。其中,二聚萘并吡喃酮、和表现出强烈的细胞毒性。进一步的机制研究表明,诱导细胞凋亡,使 PANC-1 细胞的细胞周期停滞在 G0/G1 期,引起形态变化并产生 ROS;并通过 ROS 介导的 PI3K/Akt 信号通路诱导 PANC-1 细胞凋亡。