Isolation and structural characterization of a pectin from Lycium ruthenicum Murr and its anti-pancreatic ductal adenocarcinoma cell activity

•A polysaccharide, LRP3-S1 was purified and characterized from Lycium ruthenicum.•The main chain of this polysaccharide was alternate 1,4-α-D-GalpA and 1,2-α-L-Rhap.•The side chains of LRP3-S1 contained arabinans and arabinogalactans.•LRP3-S1 inhibited the growth and invasion of pancreatic cancer ce...

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Published inCarbohydrate polymers Vol. 223; p. 115104
Main Authors Zhang, Shihai, He, Fei, Chen, Xia, Ding, Kan
Format Journal Article
LanguageEnglish
Published England Elsevier Ltd 01.11.2019
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Summary:•A polysaccharide, LRP3-S1 was purified and characterized from Lycium ruthenicum.•The main chain of this polysaccharide was alternate 1,4-α-D-GalpA and 1,2-α-L-Rhap.•The side chains of LRP3-S1 contained arabinans and arabinogalactans.•LRP3-S1 inhibited the growth and invasion of pancreatic cancer cells.•LRP3-S1 blocked the FAK/AKT/GSK-3β and p38 MAP kinase signaling pathways. Crude polysaccharides were obtained from fruits of Lycium ruthenicum Murr using hot water extraction followed by ethanol precipitation. A homogeneous polysaccharide, LRP3-S1 with a relative molecular weight of 114.8 kDa was purified by anion-exchange chromatography on DEAE Sepharose™Fast Flow and Sephacryl S-300 HR column. Monosaccharide composition analysis revealed that LRP3-S1 was composed of rhamnose, galacturonic acid, galactose, xylose and arabinose in a molar ratio of 14.4: 17.7: 26.6: 16.4: 24.9. LRP3-S1 contained a rhamnogalacturonan I (RG-I) backbone partially substituted at C-4 of rhamnose units by side chains, which included T-linked β-D-Galp, 1,3-linked β-D-Galp, 1,6-linked β-D-Galp, 1,3,6-linked β-D-Galp, 1,5-linked α-L-Araf, 1,3,5-linked α-L-Araf, T-linked α-L-Araf and T-linked β-D-Xylp. Biological activity tests showed that LRP3-S1 could inhibit the growth of pancreatic cancer cells. In addition, LRP3-S1 could attenuate invasion ability of BxPC-3 cells and down-regulate protein expression of p-FAK, p-AKT, p-GSK-3β and p-p38 MAP kinase.
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ISSN:0144-8617
1879-1344
1879-1344
DOI:10.1016/j.carbpol.2019.115104