14-3-3 proteins mediate an essential anti-apoptotic signal

被引:259
作者
Masters, SC
Fu, H
机构
[1] Emory Univ, Sch Med, Dept Pharmacol, Atlanta, GA 30322 USA
[2] Emory Univ, Sch Med, Grad Program Mol & Syst Pharmacol, Atlanta, GA 30322 USA
关键词
D O I
10.1074/jbc.M105971200
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
The 14-3-3 proteins are a family of highly conserved eukaryotic regulatory molecules that play important roles in many biological processes including cell cycle control and regulation of cell death. They are able to carry out these effects through binding and modulating the activity of a host of signaling proteins. The ability of 14-3-3 to inhibit Bad and other proapoptotic proteins argues that 14-3-3 can support cell survival. To examine this issue in a global sense, a specific inhibitor of 14-3-3/ligand interactions, difopein, was used. Difopein expression led to induction of apoptosis. Studies using various components of survival and death signaling pathways were consistent with a vital role for 14-3-3/ligand interactions in signal transduction from upstream pro-survival kinases to the core apoptotic machinery. Because these kinases often become activated during oncogenesis, the effect of difopein on cell death induced by antineoplastic drugs was examined. It was found that difopein enhances the ability of cisplatin to kill cells. These data support the model that 14-3-3, through binding to Bad and other ligands, is critical for cell survival signaling. Inhibition of 14-3-3 may represent a useful therapeutic target for treatment of cancer and other diseases involving inappropriate cell survival.
引用
收藏
页码:45193 / 45200
页数:8
相关论文
共 33 条
  • [1] AMARANTEMENDES GP, 1998, CELLS LAB MANUAL, V1
  • [2] Akt phosphorylation of BAD couples survival signals to the cell-intrinsic death machinery
    Datta, SR
    Dudek, H
    Tao, X
    Masters, S
    Fu, HA
    Gotoh, Y
    Greenberg, ME
    [J]. CELL, 1997, 91 (02) : 231 - 241
  • [3] DEL PL, 1997, SCIENCE, V278, P687
  • [4] APOPTOSIS IN CANCER-THERAPY - CROSSING THE THRESHOLD
    FISHER, DE
    [J]. CELL, 1994, 78 (04) : 539 - 542
  • [5] 14-3-3-PROTEIN HOMOLOGS REQUIRED FOR THE DNA-DAMAGE CHECKPOINT IN FISSION YEAST
    FORD, JC
    ALKHODAIRY, F
    FOTOU, E
    SHELDRICK, KS
    GRIFFITHS, DJF
    CARR, AM
    [J]. SCIENCE, 1994, 265 (5171) : 533 - 535
  • [6] 14-3-3 proteins: Structure, function, and regulation
    Fu, HA
    Subramanian, RR
    Masters, SC
    [J]. ANNUAL REVIEW OF PHARMACOLOGY AND TOXICOLOGY, 2000, 40 : 617 - 647
  • [7] 14-3-3-PROTEINS - POTENTIAL ROLES IN VESICULAR TRANSPORT AND RAS SIGNALING IN SACCHAROMYCES-CEREVISIAE
    GELPERIN, D
    WEIGLE, J
    NELSON, K
    ROSEBOOM, P
    IRIE, K
    MATSUMOTO, K
    LEMMON, S
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (25) : 11539 - 11543
  • [8] C-MYC-INDUCED APOPTOSIS IN FIBROBLASTS IS INHIBITED BY SPECIFIC CYTOKINES
    HARRINGTON, EA
    BENNETT, MR
    FANIDI, A
    EVAN, GI
    [J]. EMBO JOURNAL, 1994, 13 (14) : 3286 - 3295
  • [9] 14-3-3 proteins are required for the inhibition of Ras by exoenzyme S
    Henriksson, ML
    Trollér, U
    Hallberg, B
    [J]. BIOCHEMICAL JOURNAL, 2000, 349 : 697 - 701
  • [10] Induction of apoptosis by ASK1, a mammalian MAPKKK that activates SAPK/JNK and p38 signaling pathways
    Ichijo, H
    Nishida, E
    Irie, K
    tenDijke, P
    Saitoh, M
    Moriguchi, T
    Takagi, M
    Matsumoto, K
    Miyazono, K
    Gotoh, Y
    [J]. SCIENCE, 1997, 275 (5296) : 90 - 94