Depolymerized products of chitosan as potent inhibitors of tumor-induced angiogenesis

被引:152
作者
Prashanth, KVH [1 ]
Tharanathan, RN [1 ]
机构
[1] Cent Food Technol Res Inst, Dept Biochem & Nutr, Mysore 570020, Karnataka, India
来源
BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS | 2005年 / 1722卷 / 01期
关键词
low molecular weight chitosan; chitooligosaccharide; anti-angiogenesis; apoptosis; DNA;
D O I
10.1016/j.bbagen.2004.11.009
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
Water-soluble low-molecular weight chitosan (LMWC) and chitooligosaccharides (COs) were obtained from chitosan (16% Nacetylation) by depolymerization induced by potassium persulfate under nitrogen atmosphere for 2 h. They were characterized by IR, X-ray, HPLC and C-13-NMR. Splitting of C3/C5 signals in the latter indicated a newer conformation, and also showed prominence of acetyl groups in LMWC, may be due to cleavage between two consecutive deacetylated residues. Molecular weight of LMWC, determined by HPSEC, showed a single peak of similar to37 kDa. HPLC analysis of the solvent-extracted fraction revealed COs enriched with pentamer, hexamer and higher oligomers. The effect of LMWC and COs on the growth of Ehrlich ascites tumor (EAT) cells and tumor-induced neovascularization was studied. COs (50 mug) were more effective compared to LMWC (100 mug) and proved to be potent angioinhibitory and antitumor compounds, as shown by inhibition of angiogenesis and inducing apoptosis as a function of DNA fragmentation. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:22 / 29
页数:8
相关论文
共 40 条
[1]   PREPARATION OF N-ACETYLCHITOOLIGOSACCHARIDES FROM LYSOZYMIC HYDROLYSATES OF PARTIALLY N-ACETYLATED CHITOSANS [J].
AIBA, S .
CARBOHYDRATE RESEARCH, 1994, 261 (02) :297-306
[2]   CHITIN OLIGOSACCHARIDES ELICIT LIGNIFICATION IN WOUNDED WHEAT LEAVES [J].
BARBER, MS ;
BERTRAM, RE ;
RIDE, JP .
PHYSIOLOGICAL AND MOLECULAR PLANT PATHOLOGY, 1989, 34 (01) :3-12
[3]   Concepts for improved regioselective placement of O-sulfo, N-sulfo, N-acetyl, and N-carboxymethyl groups in chitosan derivatives [J].
Baumann, H ;
Faust, V .
CARBOHYDRATE RESEARCH, 2001, 331 (01) :43-57
[4]  
Cha SY, 2001, J POLYM SCI POL CHEM, V39, P880, DOI 10.1002/1099-0518(20010315)39:6<880::AID-POLA1062>3.0.CO
[5]  
2-K
[6]   Kinetics and products of the degradation of chitosan by hydrogen peroxide [J].
Chang, KLB ;
Tai, MC ;
Cheng, FH .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2001, 49 (10) :4845-4851
[7]   Preparation of chitosan oligomers by irradiation [J].
Choi, WS ;
Ahn, KJ ;
Lee, DW ;
Byun, MW ;
Park, HJ .
POLYMER DEGRADATION AND STABILITY, 2002, 78 (03) :533-538
[8]   A CONVENIENT ACCESS TO BETA-(1-]4)-LINKED 2-AMINO-2-DEOXY-D-GLUCOPYRANOSYL FLUORIDE OLIGOSACCHARIDES AND BETA-(1-]4)-LINKED 2-AMINO-2-DEOXY-D-GLUCOPYRANOSYL OLIGOSACCHARIDES BY FLUOROLYSIS AND FLUOROHYDROLYSIS OF CHITOSAN [J].
DEFAYE, J ;
GADELLE, A ;
PEDERSEN, C .
CARBOHYDRATE RESEARCH, 1994, 261 (02) :267-277
[9]   Structures and thermal properties of chitosan-modified poly(methyl methacrylate) [J].
Don, TM ;
Hsu, SC ;
Chiu, WY .
JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY, 2001, 39 (10) :1646-1655
[10]   SPECIFICITY OF CHITOSANASE FROM BACILLUS-PUMILUS [J].
FUKAMIZO, T ;
OHKAWA, T ;
IKEDA, Y ;
GOTO, S .
BIOCHIMICA ET BIOPHYSICA ACTA-PROTEIN STRUCTURE AND MOLECULAR ENZYMOLOGY, 1994, 1205 (02) :183-188