Glycosphingolipid antigens and cancer therapy

被引:258
作者
Hakomori, S
Zhang, YM
机构
[1] UNIV WASHINGTON, PACIFIC NW RES FDN, DEPT PATHOBIOL, SEATTLE, WA 98122 USA
[2] UNIV WASHINGTON, PACIFIC NW RES FDN, DEPT MICROBIOL, SEATTLE, WA 98122 USA
来源
CHEMISTRY & BIOLOGY | 1997年 / 4卷 / 02期
关键词
D O I
10.1016/S1074-5521(97)90253-2
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
Specific types of glycosphingolipid (GSL), which are chemically detectable in normal cells, are more highly expressed in tumors, The high level of expression on the surfaces of tumor cells causes an antibody response to these GSLs, which can therefore be described as tumor-associated antigens. Some of these GSLs have been shown to be adhesion molecules involved in tumor cell metastasis, and to be modulators of signal transduction controlling tumor cell growth and motility. Tumor-associated GSL antigens have been used in the development of antitumor vaccines. GSLs and sphingolipids involved in adhesion and signaling are therefore targets for cancer therapy.
引用
收藏
页码:97 / 104
页数:8
相关论文
共 47 条
  • [1] An antibody-interleukin 2 fusion protein overcomes tumor heterogeneity by induction of a cellular immune response
    Becker, JC
    Varki, N
    Gillies, SD
    Furukawa, K
    Reisfeld, RA
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (15) : 7826 - 7831
  • [2] BERG EL, 1991, J BIOL CHEM, V266, P14869
  • [3] TOTAL SYNTHESIS OF A HUMAN BREAST-TUMOR ASSOCIATED ANTIGEN
    BILODEAU, MT
    PARK, TK
    HU, SH
    RANDOLPH, JT
    DANISHEFSKY, SJ
    LIVINGSTON, PO
    ZHANG, SL
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1995, 117 (29) : 7840 - 7841
  • [4] THE BACTERIAL COLICIN ACTIVE AGAINST TUMOR-CELLS IN-VITRO AND IN-VIVO IS VEROTOXIN-1
    FARKASHIMSLEY, H
    HILL, R
    ROSEN, B
    ARAB, S
    LINGWOOD, CA
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (15) : 6996 - 7000
  • [5] FUKUSHI Y, 1984, J BIOL CHEM, V259, P511
  • [6] Hakomori S, 1996, CANCER RES, V56, P5309
  • [7] Hakomori S, 1996, Adv Pharmacol, V36, P155, DOI 10.1016/S1054-3589(08)60581-5
  • [8] GLYCOLIPIDS OF HAMSTER FIBROBLASTS AND DERIVED MALIGNANT-TRANSFORMED CELL LINES
    HAKOMORI, S
    MURAKAMI, WT
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1968, 59 (01) : 254 - &
  • [9] HAKOMORI SI, 1989, ADV CANCER RES, V52, P257
  • [10] SELECTIN GMP-140 (CD62, PADGEM) BINDS TO SIALOSYL-LEA AND SIALOSYL-LEX, AND SULFATED GLYCANS MODULATE THIS BINDING
    HANDA, K
    NUDELMAN, ED
    STROUD, MR
    SHIOZAWA, T
    HAKOMORI, S
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1991, 181 (03) : 1223 - 1230