Emerging roles of carbohydrates and glycomimetics in anticancer drug design

被引:57
作者
Barchi, JJ [1 ]
机构
[1] NCI, NIH, Med Chem Lab, Div Basic Sci, Bethesda, MD 20892 USA
关键词
D O I
10.2174/1381612003400876
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Tumorigenesis is accompanied by marked changes in the expression and presentation of various macromolecules at the cell surface. These tumor-associated adjustments result from the differential expression of genes coding for the production or post-translational modifications of these macromolecules during transformation to a particular tumor phenotype. In turn, tumor cells acquire distinct biophysical properties which set them apart from their normal counterparts. Alterations of carbohydrate structures and their organization on the surface of neoplastic cells is a hallmark of the tumorigenic and, most notably, the metastatic phenotype, Carbohydrate-protein and carbohydrate-carbohydrate interactions are critical events in the progression, dissemination and invasion of cancer cells. Many cell-cell contacts and subsequent remodeling of the tumor microenvironment are mediated by cell-surface glycans. The discovery of agents that modulate these interactions or interfere with the processing of tumor associated oligosaccharides is a fervent area of research today. This review will highlight the current status of the use of carbohydrate-based compounds that are being evaluated as potential anticancer therapeutics. In addition, the use of structures based on glycopeptides and carbohydrate mimetics will also be discussed.
引用
收藏
页码:485 / 501
页数:17
相关论文
共 125 条
[1]  
Allen H. J., 1992, GLYCOCONJUGATES COMP, P263
[2]  
Alvarez-Manilla G, 1999, GLYCOBIOLOGY, V9, P1130
[3]  
Bay S, 1997, J PEPT RES, V49, P620
[4]  
BOCK K, 1994, COMPLEX CARBOHYDRATE
[5]   (1->3)-beta-D-glucans as biological response modifiers: A review of structure-functional activity relationships [J].
Bohn, JA ;
BeMiller, JN .
CARBOHYDRATE POLYMERS, 1995, 28 (01) :3-14
[6]   STRUCTURE-FUNCTION STUDIES ON SELECTIN CARBOHYDRATE LIGANDS - MODIFICATIONS TO FUCOSE, SIALIC-ACID AND SULFATE AS A SIALIC-ACID REPLACEMENT [J].
BRANDLEY, BK ;
KISO, M ;
ABBAS, S ;
NIKRAD, P ;
SRIVASATAVA, O ;
FOXALL, C ;
ODA, Y ;
HASEGAWA, A .
GLYCOBIOLOGY, 1993, 3 (06) :633-641
[7]  
BREMER EG, 1984, J BIOL CHEM, V259, P4773
[8]   INHIBITION OF MUCIN SYNTHESIS BY BENZYL-ALPHA-GALNAC IN KATO-III GASTRIC-CANCER AND CACO-2 COLON-CANCER CELLS [J].
BYRD, JC ;
DAHIYA, R ;
HUANG, J ;
KIM, YS .
EUROPEAN JOURNAL OF CANCER, 1995, 31A (09) :1498-1505
[9]  
Catterall JB, 1995, CANCER J - FRANCE, V8, P320
[10]  
CHAPLEUR I, 1996, CARBOHYDRATE MIMICS