Anticancer properties of low molecular weight oat beta-glucan - An in vitro study

被引:83
作者
Choromanska, Anna [1 ]
Kulbacka, Julita [1 ]
Rembialkowska, Nina [1 ]
Pilat, Justyna [1 ]
Oledzki, Remigiusz [2 ]
Harasym, Joanna [2 ]
Saczko, Jolanta [1 ]
机构
[1] Wroclaw Med Univ, Dept Med Biochem, PL-50368 Wroclaw, Poland
[2] Wroclaw Univ Econ, Dept Food Biotechnol, PL-53345 Wroclaw, Poland
关键词
Oat beta-glucan; Melanoma; Skin cancer; PHOTODYNAMIC THERAPY; ANTITUMOR; DECTIN-1; RECEPTOR; CELLS; EXOPOLYSACCHARIDES; POLYSACCHARIDES; INDUCTION; MELANOMA; ZYMOSAN;
D O I
10.1016/j.ijbiomac.2015.05.035
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Anticancer properties of 1-3,1-4 oat beta glucan are under intensive investigation now. Antitumor characteristic of fungi and yeast beta-glucans have been widely recognized, but those polysaccharides are mostly insoluble which creates several problems especially in topical formulation. Also high molecular weight oat beta-glucans reveal high viscosity which restricts its application. According to those problems in the current study the antitumor activities of low molecular weight beta-glucan derived from oats were investigated in cancer cells: Me45, A431 and normal HaCaT and murine macrophages P388/D1. The low molecular weight beta-glucan from oat significantly deceased cancer cells viability, while for the normal cells it was non-toxic. It was observed that with the increasing incubation time and the beta-glucan concentration the cancer cells viability significantly deceased. Furthermore for the normal cells the low molecular weight beta-glucan from oat was non-toxic. Immunocytochemical ABC analysis showed that beta-glucan induced strong expression of caspase-12 in both cancer cell lines, while in HaCaT cells ABC reaction was significantly lower and in P388/D1 cell line ABC reaction was negative. Our preliminary studies show strong anti-tumor properties of new low molecular weight beta-glucan from oat and at the same time no toxicity for normal cells. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:23 / 28
页数:6
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