Involvement of Cot activity in the proliferation of ALCL lymphoma cells

被引:6
作者
Fernandez, Margarita
Manso, Rebeca
Bernaldez, Flavia
Lopez, Pilar
Martin-Duce, Antonio
Alemany, Susana
机构
[1] CSIC UAM, Inst Invest Biomed Alberto Sols, Madrid, Spain
[2] Univ Autonoma Madrid, Fac Med, Dept Bioquim, E-28049 Madrid, Spain
关键词
Cot/tpl2; Erk1/2; Lymphoma; shRNA; Proliferation; p70; S6K; REED-STERNBERG CELLS; SIGNALING PATHWAY; PROTEIN-KINASE; HODGKIN-DISEASE; MAP KINASE; ACTIVATION; CD30; INFLAMMATION; EXPRESSION; SURVIVAL;
D O I
10.1016/j.bbrc.2011.06.157
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
Anaplastic large-cell lymphoma (ALCL) cells overexpress CD30 on their cell surface, show increased levels of activated Erk1/2 and of JunB; participating JunB in the proliferative capacity of these lymphomas. Here, we show that ALCL lymphoma cells also present high expression levels of the proto-oncogenic Cot (MAP3K8). Using pharmacological drugs as well as the RNA interference technique we show that Cot protein is responsible for the constitutive Erk1/2 activation in the ALCL lymphoma cells, SUDHL-1. Besides, inhibition of Cot activity reduces the number of cell divisions which is achieved, at least in part, by the control that Cot exercises on the activation state of p70 S6K and on the expression levels of JunB. Since Cot represents an alternative mode, independently of RAF, to activate Erk1/2, all these data strongly suggest that molecular targeting of Cot may be a potential new specific strategy for ALCL lymphomas therapy, without the fully disturbance of the Erk1/2 function. (C) 2011 Published by Elsevier Inc.
引用
收藏
页码:655 / 660
页数:6
相关论文
共 32 条
  • [2] Quantitative phosphorylation profiling of the ERK/p90 ribosomal S6 kinase-signaling cassette and its targets, the tuberous sclerosis tumor suppressors
    Ballif, BA
    Roux, PP
    Gerber, SA
    MacKeigan, JP
    Blenis, J
    Gygi, SP
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (03) : 667 - 672
  • [3] Diverse Toll-like receptors utilize Tpl2 to activate extracellular signal-regulated kinase (ERK) in hemopoietic cells
    Banerjee, A
    Gugasyan, R
    McMahon, M
    Gerondakis, S
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (09) : 3274 - 3279
  • [4] A kinetic study of the murine mixed lymphocyte reaction by 5,6-carboxyfluorescein diacetate succinimidyl ester labeling
    Chen, JC
    Chang, ML
    Muench, MO
    [J]. JOURNAL OF IMMUNOLOGICAL METHODS, 2003, 279 (1-2) : 123 - 133
  • [5] Mutational activation of the MAP3K8 protooncogene in lung cancer
    Clark, AM
    Reynolds, SH
    Anderson, M
    Wiest, JS
    [J]. GENES CHROMOSOMES & CANCER, 2004, 41 (02) : 99 - 108
  • [6] Targeting protein kinases for the development of anti-inflammatory drugs
    Cohen, Philip
    [J]. CURRENT OPINION IN CELL BIOLOGY, 2009, 21 (02) : 317 - 324
  • [7] MOLECULAR-CLONING AND EXPRESSION OF A NEW MEMBER OF THE NERVE GROWTH-FACTOR RECEPTOR FAMILY THAT IS CHARACTERISTIC FOR HODGKINS-DISEASE
    DURKOP, H
    LATZA, U
    HUMMEL, M
    EITELBACH, F
    SEED, B
    STEIN, H
    [J]. CELL, 1992, 68 (03) : 421 - 427
  • [8] FALINI B, 1995, BLOOD, V85, P1
  • [9] Targeting innate immunity protein kinase signalling in inflammation
    Gaestel, Matthias
    Kotlyarov, Alexey
    Kracht, Michael
    [J]. NATURE REVIEWS DRUG DISCOVERY, 2009, 8 (06) : 480 - 499
  • [10] The COOH-terminal domain of wild-type cot regulates its stability and kinase specific activity
    Gándara, ML
    López, P
    Hernando, R
    Castaño, JG
    Alemany, S
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 2003, 23 (20) : 7377 - 7390