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螺旋青霉(Fries)多糖的结构分析及潜在抗肿瘤活性。

Structural analysis and potential anti-tumor activity of Sporisorium reilianum (Fries) polysaccharide.

机构信息

School of Life Sciences, Northeast Forestry University, Harbin 150040, PR China; Northeast Petroleum University, Daqing 163318, PR China.

School of Forestry, Northeast Forestry University, Harbin 150040, PR China.

出版信息

Int J Biol Macromol. 2020 Jun 15;153:986-994. doi: 10.1016/j.ijbiomac.2019.10.228. Epub 2019 Nov 19.

Abstract

A neutral polysaccharide WM-NP-60 was successfully isolated and purified from a phytopathogenic fungus Sporisorium reilianum (Fries). The characteristics and potential antitumor activities of WM-NP-60 were studied. WM-NP-60 was a water-soluble polysaccharide. The molecular weight of WM-NP-60 was 15.6 kDa. The main chain of WM-NP-60 was composed of β-1,6-D-Glcp and its side chains were β-1,3-D-Glcp. The side chains bound to the main chain with glycosyl groups at the C-3 positions. Gal might be attached to the backbone as a side chain or bound to the linear β-1,3-D-Glcp side chain. WM-NP-60 could inhibit the proliferation of HepG2 and SGC7901 cells in a dose-dependently manner. In addition, it was found that WM-NP-60 triggered the HepG2 and SGC7901 cell cycle arrest at the G phase and induced apoptosis of HepG2 and SGC7901 cells. Taken together, these results suggested that WM-NP-60 possessed a tumor-suppressive activity and might be regarded as a potential natural anti-tumor drug.

摘要

从植物病原菌盾壳霉(Sporisorium reilianum)(Fries)中成功分离和纯化出一种中性多糖 WM-NP-60。研究了 WM-NP-60 的特性和潜在的抗肿瘤活性。WM-NP-60 是一种水溶性多糖。WM-NP-60 的分子量为 15.6 kDa。WM-NP-60 的主链由β-1,6-D-Glcp 组成,其侧链为β-1,3-D-Glcp。侧链通过糖苷基在 C-3 位与主链结合。Gal 可能作为侧链连接到主链上,也可能与线性β-1,3-D-Glcp 侧链结合。WM-NP-60 可剂量依赖性抑制 HepG2 和 SGC7901 细胞的增殖。此外,还发现 WM-NP-60 可使 HepG2 和 SGC7901 细胞周期阻滞在 G 期,并诱导 HepG2 和 SGC7901 细胞凋亡。综上所述,这些结果表明 WM-NP-60 具有肿瘤抑制活性,可能被视为一种潜在的天然抗肿瘤药物。

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