EFFECTS OF NATURAL COMPLEX CARBOHYDRATE (CITRUS PECTIN) ON MURINE MELANOMA CELL PROPERTIES RELATED TO GALECTIN-3 FUNCTIONS

被引:149
作者
INOHARA, H [1 ]
RAZ, A [1 ]
机构
[1] MICHIGAN CANC FDN,CANC METASTASIS PROGRAM,DETROIT,MI 48201
关键词
GALECTIN-3; CITRUS PECTIN; MELANOMA;
D O I
10.1007/BF00731303
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
Citrus pectin (CP) and pH-modified citrus pectin (MCP) are highly branched and non-branched complex polysaccharides, respectively, rich in galactoside residues, capable of combining with the carbohydrate-binding domain of galectin-3. We reported previously that intravenous injection of B16-F1 murine melanoma cells with CP or MCP into syngeneic mice resulted in a significant increase or decrease of lung colonization, respectively (Platt D, Rat A (1992) J Natl Cancer Inst 84:438-42). Here we studied the effects of these polysaccharides on cell-cell and cell-matrix interactions mediated by carbohydrate-recognition. MCP, but not CP, inhibited B16-F1 melanoma cells adhesion to laminin and asialofetuin-induced homotypic aggregation. Both polysaccharides inhibited anchorage-independent growth of B16-F1 cells in semisolid medium, i.e. agarose. These resuls indicate that carbohydrate-recognition by cell surface galectin-3 may be involved in cell-extracellular matrix interaction and play a role in anchorage-independent growth as well as the in vivo embolization of tumour cells.
引用
收藏
页码:527 / 532
页数:6
相关论文
共 33 条
  • [1] ALBERSHEIM PETER, 1967, CARBOHYD RES, V5, P340, DOI 10.1016/S0008-6215(00)80510-8
  • [2] AN IGE-BINDING PROTEIN WITH A DISTINCTIVE REPETITIVE SEQUENCE AND HOMOLOGY WITH AN IGG RECEPTOR
    ALBRANDT, K
    ORIDA, NK
    LIU, FT
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (19) : 6859 - 6863
  • [3] GALECTINS - A FAMILY OF ANIMAL BETA-GALACTOSIDE-BINDING LECTINS
    BARONDES, SH
    CASTRONOVO, V
    COOPER, DNW
    CUMMINGS, RD
    DRICKAMER, K
    FEIZI, T
    GITT, MA
    HIRABAYASHI, J
    HUGHES, C
    KASAI, K
    LEFFLER, H
    LIU, FT
    LOTAN, R
    MERCURIO, AM
    MONSIGNY, M
    PILLAI, S
    POIRER, F
    RAZ, A
    RIGBY, PWJ
    RINI, JM
    WANG, JL
    [J]. CELL, 1994, 76 (04) : 597 - 598
  • [4] SOLUBLE LECTINS - A NEW CLASS OF EXTRACELLULAR PROTEINS
    BARONDES, SH
    [J]. SCIENCE, 1984, 223 (4642) : 1259 - 1264
  • [5] MOLECULAR-CLONING OF A HUMAN MACROPHAGE LECTIN SPECIFIC FOR GALACTOSE
    CHERAYIL, BJ
    CHAITOVITZ, S
    WONG, C
    PILLAI, S
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (18) : 7324 - 7328
  • [6] FIDLER IJ, 1973, EUR J CANCER, V9, P223, DOI 10.1016/S0014-2964(73)80022-2
  • [7] CELLULAR TUMORIGENICITY IN NUDE MICE - CORRELATION WITH CELL-GROWTH IN SEMISOLID MEDIUM
    FREEDMAN, VH
    SHIN, S
    [J]. CELL, 1974, 3 (04) : 355 - 359
  • [8] HO MK, 1982, J IMMUNOL, V128, P1221
  • [9] INTEGRINS - VERSATILITY, MODULATION, AND SIGNALING IN CELL-ADHESION
    HYNES, RO
    [J]. CELL, 1992, 69 (01) : 11 - 25
  • [10] JIA SH, 1988, J BIOL CHEM, V263, P6009