p38α MAP kinase as a sensor of reactive oxygen species in tumorigenesis

被引:346
作者
Dolado, Ignacio
Swat, Aneta
Ajenjo, Nuria
De Vita, Gabriella
Cuadrado, Ana
Nebreda, Angel R.
机构
[1] Spanish Natl Canc Ctr, CNIO, Madrid 28029, Spain
[2] European Mol Biol Lab, D-69117 Heidelberg, Germany
[3] CEINGE, I-80131 Naples, Italy
关键词
D O I
10.1016/j.ccr.2006.12.013
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
p38 alpha is a stress-activated protein kinase that negatively regulates malignant transformation induced by oncogenic H-Ras, although the mechanisms involved are not fully understood. Here, we show that p38 alpha is not a general inhibitor of oncogenic signaling, but that it specifically modulates transformation induced by oncogenes that produce reactive oxygen species (ROS). This inhibitory effect is due to the ROS-induced activation of p38 alpha early in the process of transformation, which induces apoptosis and prevents the accumulation of ROS and their carcinogenic effects. Accordingly, highly tumorigenic cancer cell lines have developed a mechanism to uncouple p38 alpha activation from ROS production. Our results indicate that oxidative stress sensing plays a key role in the inhibition of tumor initiation by p38 alpha.
引用
收藏
页码:191 / 205
页数:15
相关论文
共 56 条
[1]   Oxidative stress and gene regulation [J].
Allen, RG ;
Tresini, M .
FREE RADICAL BIOLOGY AND MEDICINE, 2000, 28 (03) :463-499
[2]   Differential activation of p38 mitogen-activated protein kinase isoforms depending on signal strength [J].
Alonso, G ;
Ambrosino, C ;
Jones, M ;
Nebreda, AR .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (51) :40641-40648
[3]   Negative feedback regulation of MKK6 mRNA stability by p38α mitogen-activated protein kinase [J].
Ambrosino, C ;
Mace, G ;
Galban, S ;
Fritsch, C ;
Vintersten, K ;
Black, E ;
Gorospe, M ;
Nebreda, AR .
MOLECULAR AND CELLULAR BIOLOGY, 2003, 23 (01) :370-381
[4]   DIETARY CARCINOGENS AND ANTICARCINOGENS - OXYGEN RADICALS AND DEGENERATIVE DISEASES [J].
AMES, BN .
SCIENCE, 1983, 221 (4617) :1256-1264
[5]  
BOS JL, 1989, CANCER RES, V49, P4682
[6]   Mechanism of p38 MAP kinase activation in vivo [J].
Brancho, D ;
Tanaka, N ;
Jaeschke, A ;
Ventura, JJ ;
Kelkar, N ;
Tanaka, Y ;
Kyuuma, M ;
Takeshita, T ;
Flavell, RA ;
Davis, RJ .
GENES & DEVELOPMENT, 2003, 17 (16) :1969-1978
[7]   Inactivation of the Wip1 phosphatase inhibits mammary tumorigenesis through p38 MAPK-mediated activation of the p16Ink4a-p19Arf pathway [J].
Bulavin, DV ;
Phillips, C ;
Nannenga, B ;
Timofeev, O ;
Donehower, LA ;
Anderson, CW ;
Appella, E ;
Fornace, AJ .
NATURE GENETICS, 2004, 36 (04) :343-350
[8]   Amplification of PPM1D in human tumors abrogates p53 tumor-suppressor activity [J].
Bulavin, DV ;
Demidov, ON ;
Saito, S ;
Kauraniemi, P ;
Phillips, C ;
Amundson, SA ;
Ambrosino, C ;
Sauter, G ;
Nebreda, AR ;
Anderson, CW ;
Kallioniemi, A ;
Fornace, AJ ;
Appella, E .
NATURE GENETICS, 2002, 31 (02) :210-215
[9]   The p38 pathway provides negative feedback for Ras proliferative signaling [J].
Chen, G ;
Hitomi, M ;
Han, JH ;
Stacey, DW .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (50) :38973-38980
[10]   Glutathione S-transferase Mu modulates the stress-activated signals by suppressing apoptosis signal-regulating kinase 1 [J].
Cho, SG ;
Lee, YH ;
Park, HS ;
Ryoo, K ;
Kang, KW ;
Park, J ;
Eom, SJ ;
Kim, MJ ;
Chang, TS ;
Choi, SY ;
Shim, J ;
Kim, Y ;
Dong, MS ;
Lee, MJ ;
Kim, SG ;
Ichijo, H ;
Choi, EJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (16) :12749-12755