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  5. Structural identification of a fucose-containing 1,3-β-mannoglucan from Poria cocos and its anti-lung cancer CL1-5 cells migration via inhibition of TGFβR-mediated signaling
 
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Structural identification of a fucose-containing 1,3-β-mannoglucan from Poria cocos and its anti-lung cancer CL1-5 cells migration via inhibition of TGFβR-mediated signaling

Journal
International Journal of Biological Macromolecules
Journal Volume
157
Pages
311-318
Date Issued
2020
Author(s)
Lin T.-Y.
Lu M.-K.
CHIA-CHUAN CHANG  
DOI
10.1016/j.ijbiomac.2020.04.014
URI
2-s2.0-85083865111
https://scholars.lib.ntu.edu.tw/handle/123456789/569031
Abstract
Poria cocos (Polyporacea), is a fungus used in traditional Chinese medicine. A study of the valuable sulfated polysaccharides (SPS) with the structure and pharmaceutical benefits from the mycelial culture conditions of P. cocos was attempted. The SPSs were fractionated by gel filtration chromatography to give a fucose-containing mannoglucan polysaccharide (denoted as FMGP):[Formula presented] The main skeleton was a 1,4-α-Man-interlaced-1,3-β-glucan with interlaced 6-O-α-L-fucosyl 1,4-α-Glc and 1,4-α-Gal branches. FMGP dramatically inhibited cell migration in the highly metastatic human lung cancer cell line CL1-5 cells. Mechanistically, FMGP dramatically downregulated the expression of TGFβRI and inhibited phosphorylation of FAK and AKT. Moreover, FMGP reduced the metastasis-related protein, Slug, expression. This is the first paper reporting a branched 1,3-β-mannoglucan from P. cocos and its anti-lung cancer CL1-5 cells migration activities. ? 2020
Subjects
Cancer cell migration; Poria cocos polysaccharides; Slug
SDGs

[SDGs]SDG3

Other Subjects
1,3 beta mannoglucan; antineoplastic agent; beta 1,3 glucan; focal adhesion kinase; fucose; fucose containing mannoglucan polysaccharide; polysaccharide sulfate; Poria cocos extract; protein kinase B; transcription factor Slug; transforming growth factor beta receptor 1; unclassified drug; antineoplastic agent; fucose; mannoglucan; polysaccharide; SNAI1 protein, human; transcription factor Snail; transforming growth factor beta; antineoplastic activity; Article; cancer inhibition; cell migration; CL1-5 cell line; controlled study; drug identification; drug isolation; drug structure; enzyme phosphorylation; gel filtration chromatography; human; human cell; metastasis inhibition; nonhuman; protein expression; receptor down regulation; TGF beta signaling; Wolfiporia cocos; adenocarcinoma; cell motion; cell survival; chemistry; dose response; down regulation; drug effect; fractionation; isolation and purification; lung tumor; metabolism; phosphorylation; Poria; signal transduction; tumor cell line; Adenocarcinoma; Antineoplastic Agents; Cell Line, Tumor; Cell Movement; Cell Survival; Chemical Fractionation; Dose-Response Relationship, Drug; Down-Regulation; Fucose; Humans; Lung Neoplasms; Phosphorylation; Polysaccharides; Poria; Signal Transduction; Snail Family Transcription Factors; Transforming Growth Factor beta
Type
journal article

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