PIKE-A is amplified in human cancers and prevents apoptosis by up-regulating Akt

被引:65
作者
Ahn, JY [1 ]
Hu, YX [1 ]
Kroll, TG [1 ]
Allard, P [1 ]
Ye, KQ [1 ]
机构
[1] Emory Univ, Sch Med, Dept Pathol & Lab Med, Atlanta, GA 30322 USA
关键词
D O I
10.1073/pnas.0400921101
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
PIKE-A (PIKE-activating Akt), an isoform of PIKE GTPase that enhances phosphatidylinositol 3-kinase (P13-kinase) activity, specifically binds to active Akt but not P13-kinase. PIKE-A stimulates Akt activity in a GTP-dependent manner and promotes invasiveness of cancer cell lines. Here, we show that PIKE-A is amplified in a variety of human cancers and that amplified PIKE-A directly stimulates Akt and inhibits apoptosis compared to cells with normal PIKE-A copy number. Overexpression of PIKE-A wild-type but not dominant-negative mutant stimulates Akt activity and prevents apoptosis. Moreover, knockdown of PIKE-A diminishes Akt activity and increases apoptosis. Our findings suggest that PIKE-A amplification contributes to cancer cell survival and progression by inhibiting apoptosis through up-regulating Akt.
引用
收藏
页码:6993 / 6998
页数:6
相关论文
共 33 条
  • [1] A RETROVIRAL ONCOGENE, AKT, ENCODING A SERINE-THREONINE KINASE CONTAINING AN SH2-LIKE REGION
    BELLACOSA, A
    TESTA, JR
    STAAL, SP
    TSICHLIS, PN
    [J]. SCIENCE, 1991, 254 (5029) : 274 - 277
  • [2] Protein kinase B/Akt-mediated phosphorylation promotes nuclear exclusion of the winged helix transcription factor FKHR1
    Biggs, WH
    Meisenhelder, J
    Hunter, T
    Cavenee, WK
    Arden, KC
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (13) : 7421 - 7426
  • [3] Akt promotes cell survival by phosphorylating and inhibiting a forkhead transcription factor
    Brunet, A
    Bonni, A
    Zigmond, MJ
    Lin, MZ
    Juo, P
    Hu, LS
    Anderson, MJ
    Arden, KC
    Blenis, J
    Greenberg, ME
    [J]. CELL, 1999, 96 (06) : 857 - 868
  • [4] Regulation of cell death protease caspase-9 by phosphorylation
    Cardone, MH
    Roy, N
    Stennicke, HR
    Salvesen, GS
    Franke, TF
    Stanbridge, E
    Frisch, S
    Reed, JC
    [J]. SCIENCE, 1998, 282 (5392) : 1318 - 1321
  • [5] AKT2, A PUTATIVE ONCOGENE ENCODING A MEMBER OF A SUBFAMILY OF PROTEIN-SERINE THREONINE KINASES, IS AMPLIFIED IN HUMAN OVARIAN CARCINOMAS
    CHENG, JQ
    GODWIN, AK
    BELLACOSA, A
    TAGUCHI, T
    FRANKE, TF
    HAMILTON, TC
    TSICHLIS, PN
    TESTA, JR
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (19) : 9267 - 9271
  • [6] Amplification of AKT2 in human pancreatic cancer cells and inhibition of ATK2 expression and tumorigenicity by antisense RNA
    Cheng, JQ
    Ruggeri, B
    Klein, WM
    Sonoda, G
    Altomare, DA
    Watson, DK
    Testa, JR
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (08) : 3636 - 3641
  • [7] 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
  • [8] DEL PL, 1997, SCIENCE, V278, P687
  • [9] How BAD phosphorylation is good for survival
    Downward, J
    [J]. NATURE CELL BIOLOGY, 1999, 1 (02) : E33 - E35
  • [10] CREB is a regulatory target for the protein kinase Akt/PKB
    Du, KY
    Montminy, M
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (49) : 32377 - 32379