CDIP, a novel pro-apoptotic gene, regulates TNFα-mediated apoptosis in a p53-dependent manner

被引:39
作者
Brown, Lauren
Ongusaha, Pat P.
Kim, Hyung-Gu
Nuti, Shanthy
Mandinova, Anna
Lee, Ji Won
Khosravi-Far, Roya
Aaronson, Stuart A.
Lee, Sam W.
机构
[1] Massachusetts Gen Hosp, Cutaneous Biol Res Ctr, Charlestown, MA 02129 USA
[2] Harvard Univ, Sch Med, Charlestown, MA USA
[3] Beth Israel Deaconess Med Ctr, Dept Pathol, Boston, MA 02215 USA
[4] Harvard Univ, Sch Med, Boston, MA USA
[5] Mt Sinai Sch Med, Dept Oncol Sci, New York, NY USA
关键词
apoptosis; CDIP; p53; TNF-alpha;
D O I
10.1038/sj.emboj.7601779
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
We have identified a novel pro-apoptotic p53 target gene named CDIP ( Cell Death Involved p53-target). Inhibition of CDIP abrogates p53-mediated apoptotic responses, demonstrating that CDIP is an important p53 apoptotic effector. CDIP itself potently induces apoptosis that is associated with caspase-8 cleavage, implicating the extrinsic cell death pathway in apoptosis mediated by CDIP. siRNA-directed knockdown of caspase-8 results in a severe impairment of CDIP-dependent cell death. In investigating the potential involvement of extrinsic cell death pathway in CDIP-mediated apoptosis, we found that TNF-alpha expression tightly correlates with CDIP expression, and that inhibition of TNF-alpha signaling attenuates CDIP-dependent apoptosis. We also demonstrate that TNF-alpha is upregulated in response to p53 and p53 inducing genotoxic stress, in a CDIP-dependent manner. Consistently, knockdown of TNF-alpha impairs p53-mediated stress-induced apoptosis. Together, these findings support a novel p53 -> CDIP -> TNF-alpha apoptotic pathway that directs apoptosis after exposure of cells to genotoxic stress. Thus, CDIP provides a new link between p53-mediated intrinsic and death receptor-mediated extrinsic apoptotic signaling, providing a novel target for cancer therapeutics aimed at maximizing the p53 apoptotic response of cancer cells to drug therapy.
引用
收藏
页码:3410 / 3422
页数:13
相关论文
共 34 条
  • [1] Signal transduction by tumor necrosis factor and its relatives
    Baud, V
    Karin, M
    [J]. TRENDS IN CELL BIOLOGY, 2001, 11 (09) : 372 - 377
  • [2] p53-dependent pathways of apoptosis
    Benchimol, S
    [J]. CELL DEATH AND DIFFERENTIATION, 2001, 8 (11) : 1049 - 1051
  • [3] RADIATION-INDUCED CELL-CYCLE ARREST COMPROMISED BY P21 DEFICIENCY
    BRUGAROLAS, J
    CHANDRASEKARAN, C
    GORDON, JI
    BEACH, D
    JACKS, T
    HANNON, GJ
    [J]. NATURE, 1995, 377 (6549) : 552 - 557
  • [4] Feedback inhibition of macrophage tumor necrosis factor-α production by tristetraprolin
    Carballo, E
    Lai, WS
    Blackshear, PJ
    [J]. SCIENCE, 1998, 281 (5379) : 1001 - 1005
  • [5] TNF-R1 signaling: A beautiful pathway
    Chen, GQ
    Goeddel, DV
    [J]. SCIENCE, 2002, 296 (5573) : 1634 - 1635
  • [6] MICE LACKING P21(C/P1/WAF1) UNDERGO NORMAL DEVELOPMENT, BUT ARE DEFECTIVE IN G1 CHECKPOINT CONTROL
    DENG, CX
    ZHANG, PM
    HARPER, JW
    ELLEDGE, SJ
    LEDER, P
    [J]. CELL, 1995, 82 (04) : 675 - 684
  • [7] DEFINITION OF A CONSENSUS BINDING-SITE FOR P53
    ELDEIRY, WS
    KERN, SE
    PIETENPOL, JA
    KINZLER, KW
    VOGELSTEIN, B
    [J]. NATURE GENETICS, 1992, 1 (01) : 45 - 49
  • [8] WAF1, A POTENTIAL MEDIATOR OF P53 TUMOR SUPPRESSION
    ELDEIRY, WS
    TOKINO, T
    VELCULESCU, VE
    LEVY, DB
    PARSONS, R
    TRENT, JM
    LIN, D
    MERCER, WE
    KINZLER, KW
    VOGELSTEIN, B
    [J]. CELL, 1993, 75 (04) : 817 - 825
  • [9] Fas is involved in the p53-dependent apoptotic response to ionizing radiation in mouse testis
    Embree-Ku, M
    Venturini, D
    Boekelheide, K
    [J]. BIOLOGY OF REPRODUCTION, 2002, 66 (05) : 1456 - 1461
  • [10] Involvement of the CD95 (APO-1/Fas) receptor/ligand system in drug-induced apoptosis in leukemia cells
    Friesen, C
    Herr, I
    Krammer, PH
    Debatin, KM
    [J]. NATURE MEDICINE, 1996, 2 (05) : 574 - 577