MOLECULAR MECHANISMS OF TUMOR NECROSIS FACTOR-INDUCED CYTOTOXICITY - WHAT WE DO UNDERSTAND AND WHAT WE DO NOT

被引:239
作者
BEYAERT, R [1 ]
FIERS, W [1 ]
机构
[1] STATE UNIV GHENT,MOLEC BIOL LAB,B-9000 GHENT,BELGIUM
关键词
TNF; CYTOTOXICITY; PHOSPHOLIPASES; MITOCHONDRIA; PHOSPHORYLATION; SIGNAL TRANSDUCTION;
D O I
10.1016/0014-5793(94)80163-0
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
Although TNF plays an important role in several physiological and pathological conditions, the hallmark of this important cytokine has been its selective cytotoxic activity on tumor cells. Since its cloning in 1984, understanding of how TNF selectively kills tumor cells has been the subject of research in many laboratories. Here we review TNF-induced post-receptor signaling mechanisms which seem to be involved in the pathway to cytotoxicity.
引用
收藏
页码:9 / 16
页数:8
相关论文
共 87 条
  • [1] AGARWAL S, 1988, J IMMUNOL, V140, P4187
  • [2] ALEXANDER RB, 1987, CANCER RES, V47, P2403
  • [3] BELLOMO G, 1992, CANCER RES, V52, P1342
  • [4] INOSITOL PHOSPHATES AND CELL SIGNALING
    BERRIDGE, MJ
    IRVINE, RF
    [J]. NATURE, 1989, 341 (6239) : 197 - 205
  • [5] BEUTLER B, 1992, TUMOR NECROSIS FACTO, V10, P411
  • [6] BEYAERT R, 1993, CANCER RES, V53, P2623
  • [7] BEYAERT R, 1993, J IMMUNOL, V151, P291
  • [8] INHIBITION BY GLUCOCORTICOIDS OF TUMOR NECROSIS FACTOR-MEDIATED CYTOTOXICITY - EVIDENCE AGAINST LIPOCORTIN INVOLVEMENT
    BEYAERT, R
    SUFFYS, P
    VANROY, F
    FIERS, W
    [J]. FEBS LETTERS, 1990, 262 (01) : 93 - 96
  • [9] LITHIUM-CHLORIDE POTENTIATES TUMOR-NECROSIS-FACTOR INDUCED AND INTERLEUKIN-1 INDUCED CYTOKINE AND CYTOKINE RECEPTOR EXPRESSION
    BEYAERT, R
    SCHULZEOSTHOFF, K
    VANROY, F
    FIERS, W
    [J]. CYTOKINE, 1991, 3 (04) : 284 - 291
  • [10] LITHIUM-CHLORIDE POTENTIATES TUMOR NECROSIS FACTOR-MEDIATED CYTO-TOXICITY INVITRO AND INVIVO
    BEYAERT, R
    VANHAESEBROECK, B
    SUFFYS, P
    VANROY, F
    FIERS, W
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (23) : 9494 - 9498