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Fucoidan MF4 from Fucus vesiculosus inhibits Lewis lung cancer via STING–TBK1–IRF3 pathway

  • Chuanqin Shi
  • , Shihua Zhao
  • , Liyan Mi
  • , Deying Niu
  • , Fanwen Hu
  • , Wenwei Han
  • , Bing Li
  • Qingdao University
  • Zibo Central Hospital
  • The Affiliated Yantai Yuhuangding Hospital of Qingdao University
  • Jinan Dermatosis Prevention and Contorl Hospital

科研成果: 期刊稿件文章同行评审

15 引用 (Scopus)

摘要

Fucoidan, a sulfated polysaccharide of marine origin found in brown algae and sea cucumbers, has been identified as a neuroprotective compound. In this study, a novel fucoidan MF4 was extracted from Fucus vesiculosus and isolated using Q-Sepharose fast-flow ion-exchange chromatography. The physicochemical properties of MF4 were characterized. MF4 is primarily composed of fucose, xylose, galactose, glucose, and mannose in a molar ratio of 12.3: 4.9: 1.1: 1.0: 1.1, with an average molecular weight of 67.7 kDa. Notably, MF4 demonstrated suppression of LLC tumor growth in vivo. RNA-sequencing analysis revealed that MF4 enhanced the expression of type I interferon–associated downstream genes in macrophages. Furthermore, MF4 increased the levels of phosphorylated TBK1 and IRF3 proteins in vitro. By activating the STING–TBK1–IRF3 signaling pathway, MF4 may enhance the antitumor activity of macrophages. Taken together, MF4 has promising potential as an antitumor and immunomodulatory agent.

源语言英语
文章编号131336
期刊International Journal of Biological Macromolecules
267
DOI
出版状态已出版 - 5月 2024

联合国可持续发展目标

此成果有助于实现下列可持续发展目标:

  1. 可持续发展目标 3 - 良好健康与福祉
    可持续发展目标 3 良好健康与福祉
  2. 可持续发展目标 14 - 水下生物
    可持续发展目标 14 水下生物

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