Reactive oxygen species and HIF-1 signalling in cancer

被引:230
作者
Galanis, Alex [1 ]
Pappa, Aglaia [1 ]
Giannakakis, Antonis [1 ]
Lanitis, Evripidis [1 ]
Dangaj, Denarda [1 ]
Sandaltzopoulos, Raphael [1 ]
机构
[1] Democritus Univ Thrace, Dept Mol Biol & Genet, Lab Gene Express Mol Diag & Modern Therapeut, Alexandroupolis 68100, Greece
关键词
HIF-1; signalling; reactive oxygen species; cancer; ERK/MEK; PI3K; PKB/Akt; mTOR; protein hydroxylation;
D O I
10.1016/j.canlet.2008.02.028
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
The heterodimeric transcription factor HIF-1 (hypoxia-inducible factor 1) represents the key mediator of hypoxia response. HIF-1 controls numerous genes of pivotal importance for cellular metabolism, angiogenesis, cell cycle regulation and inhibition of apoptosis. HIF-1 overexpression and enhanced transcriptional activity are linked to tumour initiation and progression. Malfunction of the HIF-1 signalling network has been associated with breast, ovarian and prostate cancers. Elevated reactive oxygen species (ROS), also observed in such tumours, have been implicated in HIF-1 signalling. Deciphering the role of ROS in cancer onset and their involvement in signalling networks should prove invaluable for the design of novel anticancer therapeutics. (c) 2008 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:12 / 20
页数:9
相关论文
共 55 条
[1]
Interaction between HIF-1α (ODD) and hARD1 does not induce acetylation and destabilization of HIF-1α [J].
Arnesen, T ;
Kong, X ;
Evjenth, R ;
Gromyko, D ;
Varhaug, JE ;
Lin, Z ;
Sang, NL ;
Caro, J ;
Lillehaug, JR .
FEBS LETTERS, 2005, 579 (28) :6428-6432
[2]
Sumoylation increases HIF-1 stability and its transcriptional activity [J].
Bae, SH ;
Jeong, JW ;
Park, JA ;
Kim, SH ;
Bae, MK ;
Choi, SJ ;
Kim, KW .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2004, 324 (01) :394-400
[3]
OS-9 interacts with hypoxia-inducible factor 1α and prolyl hydroxylases to promote oxygen-dependent degradation of HIF-1α [J].
Baek, JH ;
Mahon, PC ;
Oh, J ;
Kelly, B ;
Krishnamachary, B ;
Pearson, M ;
Chan, DA ;
Giaccia, AJ ;
Semenza, GL .
MOLECULAR CELL, 2005, 17 (04) :503-512
[4]
Growth factor-mediated induction of HDM2 positively regulates hypoxia-inducible factor 1α expression [J].
Bárdos, JI ;
Chau, NM ;
Ashcroft, M .
MOLECULAR AND CELLULAR BIOLOGY, 2004, 24 (07) :2905-2914
[5]
The Qo site of the mitochondrial complex III is required for the transduction of hypoxic signaling via reactive oxygen species production [J].
Bell, Eric L. ;
Klimova, Tatyana A. ;
Eisenbart, James ;
Moraes, Carlos T. ;
Murphy, Michael P. ;
Budinger, G. R. Scott ;
Chandel, Navdeep S. .
JOURNAL OF CELL BIOLOGY, 2007, 177 (06) :1029-1036
[6]
Identification of hundreds of conserved and nonconserved human microRNAs [J].
Bentwich, I ;
Avniel, A ;
Karov, Y ;
Aharonov, R ;
Gilad, S ;
Barad, O ;
Barzilai, A ;
Einat, P ;
Einav, U ;
Meiri, E ;
Sharon, E ;
Spector, Y ;
Bentwich, Z .
NATURE GENETICS, 2005, 37 (07) :766-770
[7]
Phylogenetic shadowing and computational identification of human microRNA genes [J].
Berezikov, E ;
Guryev, V ;
van de Belt, J ;
Wienholds, E ;
Plasterk, RHA ;
Cuppen, E .
CELL, 2005, 120 (01) :21-24
[8]
SUMOylation of hypoxia-inducible factor-lα reduces its transcriptional activity [J].
Berta, Melanie A. ;
Mazure, Nathalie ;
Hattab, Maurice ;
Pouyssegur, Jacques ;
Brahimi-Horn, M. Christiane .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2007, 360 (03) :646-652
[9]
Arrest-defective-1 protein, an acetyltransferase, does not alter stability of hypoxia-inducible factor (HIF)-1α and is not induced by hypoxia or HIF [J].
Bilton, R ;
Mazure, N ;
Trottier, E ;
Hattab, M ;
Déry, MA ;
Richard, DE ;
Pouysségur, J ;
Brahimi-Horn, MC .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (35) :31132-31140
[10]
Hypoxia-inducible factor-1α is associated with angiogenesis, and expression of bFGF, PDGF-BB, and EGFR in invasive breast cancer [J].
Bos, R ;
van Diest, PJ ;
de Jong, JS ;
van der Groep, P ;
van der Valk, P ;
van der Wall, E .
HISTOPATHOLOGY, 2005, 46 (01) :31-36