Anticancer activity in vitro of a fucoidan from the brown alga Fucus evanescens and its low-molecular fragments, structurally characterized by tandem mass-spectrometry

被引:80
作者
Anastyuk, Stanislav D. [1 ]
Shevchenko, Natalia M. [1 ]
Ermakova, Svetlana P. [1 ]
Vishchuk, Olesya S. [1 ]
Nazarenko, Evgeny L. [1 ]
Dmitrenok, Pavel S. [1 ]
Zvyagintseva, Tatyana N. [1 ]
机构
[1] Russian Acad Sci, Pacific Inst Bioorgan Chem, Vladivostok 690022, Russia
关键词
Fucoidan derivatives; Structure; MS/MS; Anticancer activity; ANTITUMOR; OLIGOSACCHARIDES; POLYSACCHARIDES; TRANSFORMATION; CARBOHYDRATE; CONSTITUENTS; HYDROLYSIS; SULFATE; WEIGHT; FUCAN;
D O I
10.1016/j.carbpol.2011.07.036
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Fucoidan was isolated and purified from the brown algae Fucus evanescens and subjected to autohydrolysis to obtain low-molecular-weight fragments. MALDI-TOFMS analysis has shown that monosulfated fucose and more heavily sulfated (up to 5) fucooligosaccharides with polymerization degree (DP) 2, 4 and 6, including galactose-containing sulfated oligosaccharides were the products of autohydrolysis. The structural features of these fragments were elucidated by negative-ion potential lift tandem MALDI-TOF mass-spectrometry using arabinoosazone as a matrix, which allowed reducing the in-source fragmentation. Native fucoidan has been shown to exert anticancer activities in both human malignant melanoma cell lines SK-MEL-28 and SK-MEL-5. Low-molecular-weight fragments exhibited almost no action to cell proliferation in both cell lines and colony formation on SK-MEL-5 cells, but its inhibition activity to the colony formation of SK-MEL-28 cell lines was as high as was demonstrated by native fucoidan (70%). Probably, the inhibiting activity for SK-MEL-28 depended on the presence of sulfates and (1 -> 4)-linked alpha-L-Fucp residues in the main chain of fucoidan/oligosaccharides. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:186 / 194
页数:9
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