Yoshimoto Miwa, Higaki Katsumi, Nanba Eiji, Ikeguchi Masahide
Division of Surgical Oncology, Department of Surgery, School of Medicine, Tottori University Faculty of Medicine, Yonago 683-8504,Japan.
†Division of Functional Genomics, Research Center for Bioscience and Technology, Tottori University, Yonago 683-8503,Japan.
Yonago Acta Med. 2015 Mar;58(1):1-7. Epub 2015 Mar 27.
Fucoidan is a high-molecular polysaccharide whose main constituent is sulfated fucose. We specifically focused on the anti-proliferation activity of fucoidan and examined the underlying mechanism in MKN45 gastric cancer cells.
MKN45 cell proliferation was analyzed by BrdU assay and fucoidan cytotoxicity was examined by LDH and clonogenic assays. The Agilent Human microarray kit was used to identify upregulated and downregulated genes in response to fucoidan, and western blot analyses evaluated cell cycle proteins.
Fucoidan impeded the MKN45 cell cycle by approximately 50%, and inhibited cell proliferation.LDH assays showed no immediate cytotoxic effects of fucoidan at 24 h exposure, however longer time courses revealed cell growth inhibition at 4 days in a dose-dependent manner. Microarray analysis identified MAP3K5, or ASK1 (apoptosis signal-regulating kinase),which was upregulated by 1.38-fold upon fucoidan treatment.Fucoidan increased ASK1 protein levels, while reducing phosphorylated ASK1 levels. Reduction of ASK1 by siRNA decreased proliferation of MKN45 cells.
Our findings show that fucoidan may suppress cellular proliferation and DNA synthesis in MKN45 cells by suppressing the ASK1-p38 signaling pathway through reduction of phosphorylated ASK1 levels.
岩藻依聚糖是一种高分子多糖,其主要成分是硫酸化岩藻糖。我们特别关注岩藻依聚糖的抗增殖活性,并研究了其在MKN45胃癌细胞中的潜在机制。
通过BrdU检测分析MKN45细胞增殖,通过LDH和克隆形成检测检测岩藻依聚糖的细胞毒性。使用安捷伦人类微阵列试剂盒鉴定对岩藻依聚糖有反应的上调和下调基因,蛋白质印迹分析评估细胞周期蛋白。
岩藻依聚糖使MKN45细胞周期阻滞约50%,并抑制细胞增殖。LDH检测显示,暴露24小时时岩藻依聚糖没有立即产生细胞毒性作用,然而更长的时间进程显示在第4天以剂量依赖性方式抑制细胞生长。微阵列分析鉴定出丝裂原活化蛋白激酶激酶激酶5(MAP3K5)或凋亡信号调节激酶1(ASK1),在岩藻依聚糖处理后上调了1.38倍。岩藻依聚糖增加ASK1蛋白水平,同时降低磷酸化ASK1水平。通过小干扰RNA(siRNA)降低ASK1可减少MKN45细胞的增殖。
我们的研究结果表明,岩藻依聚糖可能通过降低磷酸化ASK1水平抑制ASK1-p38信号通路,从而抑制MKN45细胞的细胞增殖和DNA合成。