5-Lipoxygenase regulates senescence-like growth arrest by promoting ROS-dependent p53 activation

被引:98
作者
Catalano, A
Rodilossi, S
Caprari, P
Coppola, V
Procopio, A
机构
[1] Univ Politecn Marche, Dipartimento Patol Mol & Terapie Innovat, I-60131 Ancona, Italy
[2] Italian Natl Res Ctr Aging, Lab Cytol, Ancona, Italy
[3] NCI, Neural Dev Grp, Mouse Canc Genet Program, Frederick, MD 21701 USA
关键词
5-lipoxygenase; oncogenic ras; p53; reactive oxygen species; senescence;
D O I
10.1038/sj.emboj.7600502
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
5- Lipoxygenase ( 5LO) is involved in the production of leukotrienes and reactive oxygen species ( ROS) from arachidonic acid. Its strong activation has been associated with several diseases like cancer and neurodegeneration. Here we show that 5LO activity increases during senescence-like growth arrest induced by oncogenic ras or culture history in both human and mouse embryo fibroblasts. Overexpression of 5LO promotes senescence- like growth arrest via a p53/ p21- dependent pathway, and this occurs independently of telomerase activity. 5LO stabilizes p53 through phosphorylation at Ser15 and increases expression of the p53- transcriptional target p21. This is achieved by regulating ROS production. Indeed, ROS are increased in 5LO- arrested cells. Antioxidants and a low oxygen environment prevent 5LO- induced growth arrest. Finally, 5LO inhibition reduces the growth arrest induced by oncogenic ras or culture history and these effects are neutralized by the addition of exogenous ROS. These data link the 5LO pathway to oxidative crises of primary fibroblast and suggest that the ability of 5LO to induce senescence- like growth arrest may be important in the pathogenesis of 5LO- associated disorders.
引用
收藏
页码:170 / 179
页数:10
相关论文
共 41 条
  • [1] Coupling of boswellic acid-induced Ca2+ mobilisation and MAPK activation to lipid metabolism and peroxide formation in human leucocytes
    Altmann, A
    Poeckel, D
    Fischer, L
    Schubert-Zsilavecz, M
    Steinhilber, D
    Werz, O
    [J]. BRITISH JOURNAL OF PHARMACOLOGY, 2004, 141 (02) : 223 - 232
  • [2] Post-translational modifications and activation of p53 by genotoxic stresses
    Appella, E
    Anderson, CW
    [J]. EUROPEAN JOURNAL OF BIOCHEMISTRY, 2001, 268 (10): : 2764 - 2772
  • [3] N-t-butyl hydroxylamine, a hydrolysis product of α-phenyl-N-t-butyl nitrone, is more potent in delaying senescence in human lung fibroblasts
    Atamna, H
    Paler-Martínez, A
    Ames, BN
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (10) : 6741 - 6748
  • [4] Deconstructing PML-induced premature senescence
    Bischof, O
    Kirsh, O
    Pearson, M
    Itahana, K
    Pelicci, PG
    Dejean, A
    [J]. EMBO JOURNAL, 2002, 21 (13) : 3358 - 3369
  • [5] Tumor suppressors and oncogenes in cellular senescence
    Bringold, F
    Serrano, M
    [J]. EXPERIMENTAL GERONTOLOGY, 2000, 35 (03) : 317 - 329
  • [6] Phosphorylation of human p53 by p38 kinase coordinates N-terminal phosphorylation and apoptosis in response to UV radiation
    Bulavin, DV
    Saito, S
    Hollander, MC
    Sakaguchi, K
    Anderson, CW
    Appella, E
    Fornace, AJ
    [J]. EMBO JOURNAL, 1999, 18 (23) : 6845 - 6854
  • [7] Cellular senescence as a tumor-suppressor mechanism
    Campisi, J
    [J]. TRENDS IN CELL BIOLOGY, 2001, 11 (11) : S27 - S31
  • [8] 5-Lipoxygenase antagonizes genotoxic stress-induced apoptosis by altering p53 nuclear trafficking
    Catalano, A
    Caprari, P
    Soddu, S
    Procopio, A
    Romano, M
    [J]. FASEB JOURNAL, 2004, 18 (12) : 1740 - +
  • [9] ROLE OF LEUKOTRIENES REVEALED BY TARGETED DISRUPTION OF THE 5-LIPOXYGENASE GENE
    CHEN, XS
    SHELLER, JR
    JOHNSON, EN
    FUNK, CD
    [J]. NATURE, 1994, 372 (6502) : 179 - 182
  • [10] Homeodomain-interacting protein kinase-2 phosphorylates p53 at Ser 46 and mediates apoptosis
    D'Orazi, G
    Cecchinelli, B
    Bruno, T
    Manni, I
    Higashimoto, Y
    Saito, S
    Gostissa, M
    Coen, S
    Marchetti, A
    Del Sal, G
    Piaggio, G
    Fanciulli, M
    Appella, E
    Soddu, S
    [J]. NATURE CELL BIOLOGY, 2002, 4 (01) : 11 - 19