Strong electronic charge as an important factor for anticancer activity of chitooligosaccharides (COS)

被引:153
作者
Huang, R
Mendis, E
Rajapakse, N
Kim, SK [1 ]
机构
[1] Pukyong Natl Univ, Dept Chem, Pusan 608737, South Korea
[2] Pukyong Natl Univ, Marine Bioproc Res Ctr, Pusan 608737, South Korea
[3] Wuhan Univ, Dept Water Chem, Wuhan 430072, Peoples R China
关键词
chitooligosaccharides (COS); electronic charge; anticancer activity; necrosis;
D O I
10.1016/j.lfs.2005.09.039
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 [基础医学];
摘要
Even though several studies report the importance of chitosan derivatives for their anticancer activity, no clear information is available to describe the relationship between their charge properties and observed activities. In this research, differently charged chitooligosaccharide (COS) derivatives were synthesized and their anticancer activities were studied using three cancer cell lines, HeLa, Hep3B and SW480. Neutral red and MTT cell viability studies revealed that, highly charged COS derivatives could significantly reduce cancer cell viability, regardless to the positive or negative charge. Further, fluorescence microscopic observations and DNA fragmentation studies confirmed that the anticancer effect of these highly charged COS derivatives were due to necrosis. However, the exact molecular mechanism for anticancer activity of strongly charged COS compared to their poorly charged counterparts is not clear. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:2399 / 2408
页数:10
相关论文
共 21 条
[1]
DNA fragmentation, apoptosis and cell cycle arrest induced by zearalenone in cultured DOK, Vero and Caco-2 cells: prevention by Vitamin E [J].
Abid-Essefi, S ;
Baudrimont, I ;
Hassen, W ;
Ouanes, Z ;
Mobio, TA ;
Anane, R ;
Creppy, EE ;
Bacha, H .
TOXICOLOGY, 2003, 192 (2-3) :237-248
[2]
TOXICITY DETERMINED INVITRO BY MORPHOLOGICAL ALTERATIONS AND NEUTRAL RED ABSORPTION [J].
BORENFREUND, E ;
PUERNER, JA .
TOXICOLOGY LETTERS, 1985, 24 (2-3) :119-124
[3]
Novel pH, ion sensitive polyampholyte gels based on carboxymethyl chitosan and gelatin [J].
Chen, LY ;
Du, YM ;
Huang, RH .
POLYMER INTERNATIONAL, 2003, 52 (01) :56-61
[4]
DAVID JH, 1999, MASS SPECTROM REV, V18, P349
[5]
RE-EXAMINATION AND FURTHER DEVELOPMENT OF A PRECISE AND RAPID DYE METHOD FOR MEASURING CELL-GROWTH CELL KILL [J].
HANSEN, MB ;
NIELSEN, SE ;
BERG, K .
JOURNAL OF IMMUNOLOGICAL METHODS, 1989, 119 (02) :203-210
[6]
HENRY LM, 1998, BIOCHIM BIOPHYS ACTA, V1404, P367
[7]
PREPARATION FROM CHITIN OF (1-]4)-2-AMINO-2-DEOXY-BETA-D-GLUCOPYRANURONAN AND ITS 2-SULFOAMINO ANALOG HAVING BLOOD ANTICOAGULANT PROPERTIES [J].
HORTON, D ;
JUST, EK .
CARBOHYDRATE RESEARCH, 1973, 29 (01) :173-179
[8]
Improvement of ACE inhibitory activity of chitooligosaccharides (COS) by carboxyl modification [J].
Huang, R ;
Mendis, E ;
Kim, SK .
BIOORGANIC & MEDICINAL CHEMISTRY, 2005, 13 (11) :3649-3655
[9]
HUANG R, 2003, CARBOHYD POLYM, V51, P531
[10]
Influence of functional groups on the in vitro anticoagulant activity of chitosan sulfate [J].
Huang, RH ;
Du, YM ;
Yang, JH ;
Fan, LH .
CARBOHYDRATE RESEARCH, 2003, 338 (06) :483-489