Regulation of catalase expression in healthy and cancerous cells

被引:196
作者
Glorieux, Christophe [1 ]
Zamocky, Marcel [2 ,3 ]
Sandoval, Juan Marcelo [1 ]
Verrax, Julien [1 ]
Calderon, Pedro Buc [1 ,4 ]
机构
[1] Catholic Univ Louvain, Louvain Drug Res Inst, Toxicol & Canc Biol Res Grp, B-1200 Brussels, Belgium
[2] Univ Nat Resources & Life Sci BOKU, Dept Chem, Div Biochem, A-1190 Vienna, Austria
[3] Slovak Acad Sci, Inst Mol Biol, SK-84551 Bratislava, Slovakia
[4] Univ Arturo Prat, Fac Ciencias Salud, Iquique 1100000, Chile
关键词
Catalase; Transcription regulation; Cancer; Transcription factors; Catalase promoter; Free radicals; MANGANESE-SUPEROXIDE-DISMUTASE; ANTIOXIDANT ENZYME EXPRESSION; TATA-LESS PROMOTER; PROLIFERATOR-ACTIVATED RECEPTORS; TRANSCRIPTION FACTOR FOXO3A; WILMS-TUMOR SUPPRESSOR; OXIDATIVE STRESS; HYDROGEN-PEROXIDE; GENE-EXPRESSION; REACTIVE OXYGEN;
D O I
10.1016/j.freeradbiomed.2015.06.017
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
Catalase is an important antioxidant enzyme that dismutates hydrogen peroxide into water and molecular oxygen. The catalase gene has all the characteristics of a housekeeping gene (no TATA box, no initiator element sequence, high GC content in promoter) and a core promoter that is highly conserved among species. We demonstrate in this review that within this core promoter, the presence of DNA binding sites for transcription factors, such as NF-Y and Spl, plays an essential role in the positive regulation of catalase expression. Additional transcription factors, such as FoxO3a, are also involved in this regulatory process. There is strong evidence that the protein Akt/PKB in the PI3K signaling pathway plays a major role in the expression of catalase by modulating the activity of FoxO3a. Over the past decade, other transcription factors (PPAR gamma, Oct-1, etc.), as well as genetic, epigenetic, and posttranscriptional processes, have emerged as crucial contributors to the regulation of catalase expression. Altered expression levels of catalase have been reported in cancer tissues compared to their normal counterparts. Deciphering the molecular mechanisms that regulate catalase expression could, therefore, be of crucial importance for the future development of pro-oxidant cancer chemotherapy. (C) 2015 Published by Elsevier Inc.
引用
收藏
页码:84 / 97
页数:14
相关论文
共 214 条
  • [1] FUNCTIONAL-SIGNIFICANCE OF AN OVERLAPPING CONSENSUS BINDING MOTIF FOR SP1 AND ZIF268 IN THE MURINE ADENOSINE-DEAMINASE GENE PROMOTER
    ACKERMAN, SL
    MINDEN, AG
    WILLIAMS, GT
    BOBONIS, C
    YEUNG, CY
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (17) : 7523 - 7527
  • [2] Associations between breast cancer risk and the catalase genotype, fruit and vegetable consumption, and supplement use
    Ahn, J
    Gammon, MD
    Santella, RM
    Gaudet, MM
    Britton, JA
    Teitelbaum, SL
    Terry, MB
    Nowell, S
    Davis, W
    Garza, C
    Neugut, AI
    Ambrosone, CB
    [J]. AMERICAN JOURNAL OF EPIDEMIOLOGY, 2005, 162 (10) : 943 - 952
  • [3] Tumour suppressor PTEN enhanced enzyme activity of GPx, SOD and catalase by suppression of PI3K/AKT pathway in non-small cell lung cancer cell lines
    Akca, Hakan
    Demiray, Aydin
    Aslan, Mutay
    Acikbas, Ibrahim
    Tokgun, Onur
    [J]. JOURNAL OF ENZYME INHIBITION AND MEDICINAL CHEMISTRY, 2013, 28 (03) : 539 - 544
  • [4] RESISTANCE TO HYDROGEN-PEROXIDE ASSOCIATED WITH ALTERED CATALASE MESSENGER-RNA STABILITY IN MCF7 BREAST-CANCER CELLS
    AKMAN, SA
    FORREST, G
    CHU, FF
    DOROSHOW, JH
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA, 1989, 1009 (01) : 70 - 74
  • [5] The Molecular Mechanism of the Catalase Reaction
    Alfonso-Prieto, Mercedes
    Biarnes, Xevi
    Vidossich, Pietro
    Rovira, Carme
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2009, 131 (33) : 11751 - 11761
  • [6] Baker AM, 1997, PROSTATE, V32, P229, DOI 10.1002/(SICI)1097-0045(19970901)32:4<229::AID-PROS1>3.0.CO
  • [7] 2-E
  • [8] 11P13 DELETION AND REDUCED RBC CATALASE IN A PATIENT WITH ANIRIDIA, GLAUCOMA AND BILATERAL WILMS TUMOR
    BARLETTA, C
    CASTELLO, MA
    FERRANTE, E
    MAVELLI, I
    CLERICO, A
    CIRIOLO, MR
    VIGNETTI, P
    [J]. TUMORI, 1985, 71 (02) : 119 - 121
  • [9] Bauer G, 2012, ANTICANCER RES, V32, P2599
  • [10] Ascorbate/menadione-induced oxidative stress kills cancer cells that express normal or mutated forms of the oncogenic protein Bcr-Abl. An in vitro and in vivo mechanistic study
    Beck, Raphael
    Pedrosa, Rozangela Curi
    Dejeans, Nicolas
    Glorieux, Christophe
    Leveque, Philippe
    Gallez, Bernard
    Taper, Henryk
    Eeckhoudt, Stephane
    Knoops, Laurent
    Buc Calderon, Pedro
    Verrax, Julien
    [J]. INVESTIGATIONAL NEW DRUGS, 2011, 29 (05) : 891 - 900