Mitochondrial superoxide dismutase: A promising target for new anticancer therapies

被引:71
作者
Pani, G [1 ]
Colavitti, R [1 ]
Bedogni, B [1 ]
Fusco, S [1 ]
Ferraro, D [1 ]
Borrello, S [1 ]
Galeotti, T [1 ]
机构
[1] Catholic Univ, Sch Med, Inst Gen Pathol, Rome, Italy
关键词
D O I
10.2174/0929867043365297
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
Compelling experimental and epidemiological evidence involves oxygen radicals in carcinogenesis, acting reactive oxygen species both as endogenous genotoxins during cell initiation and as messenger molecules in mitogenesis and in tumor promotion. Moreover, oxidants stimulate neoangiogenesis. which is a prerequisite for tumor growth. However, while several natural as well as synthetic antioxidant. compounds appear to be chemopreventive in mutagenicity assays, antioxidant-based treatments for the prevention or cure of cancer have led to non-conclusive if not disappointing results. This is likely due to the fact that oxygen radicals have also a major role in the natural defences against the propagation of cancer cells, i.e. tumor cell apoptosis and immune surveillance, and mediate the beneficial cytotoxic effect of both the chemo-and radio-therapy. In recent years, the mitochondrial antioxidant enzyme, Manganous Superoxide Dismutase (MnSOD), has received a growing attention as a negative modulator Of Cellular apoptosis and as a survival factor for cancer cells. In fact, while overexpression of this enzyme in cancer cells decreases proliferation and tumor incidence in transgenic models, it is clear that even small amounts of this enzyme are Crucial for cell resistance to inflammatory stimuli and anticancer drugs, and prevent oncogene-induced apoptosis triggered by the tumor suppressor protein p53. A previously unexpected oncogenic potential of MnSOD is also suggested by the elevated levels of this enzyme in several classes of human neoplasms, in a fashion which often correlates with the degree of their malignancy. This review focuses on the debated issue of the pro- and/or anti-tumoral effect of MnSOD, with special emphasis on recent observations suggesting that pharmacological inhibition of MnSOD may represent an effective strategy to selectively kill cancer cells and to circumvent their resistance to the commonly used anticancer treatments.
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页码:1299 / 1308
页数:10
相关论文
共 116 条
[1]   Vascular endothelial growth factor induces manganese-superoxide dismutase expression in endothelial cells by a Rac1-regulated NADPH oxidase-dependent mechanism [J].
Abid, MR ;
Tsai, JC ;
Spokes, KC ;
Deshpande, SS ;
Irani, K ;
Aird, WC .
FASEB JOURNAL, 2001, 15 (11) :2548-+
[2]  
Ambrosone CB, 1999, CANCER RES, V59, P602
[3]   THE CAUSES AND PREVENTION OF CANCER [J].
AMES, BN ;
GOLD, LS ;
WILLETT, WC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (12) :5258-5265
[4]   Reactive oxygen generated by Nox1 triggers the angiogenic switch [J].
Arbiser, JL ;
Petros, J ;
Klafter, R ;
Govindajaran, B ;
McLaughlin, ER ;
Brown, LF ;
Cohen, C ;
Moses, M ;
Kilroy, S ;
Arnold, RS ;
Lambeth, JD .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (02) :715-720
[5]   ASPECTS OF THE STRUCTURE, FUNCTION, AND APPLICATIONS OF SUPEROXIDE-DISMUTASE [J].
BANNISTER, JV ;
BANNISTER, WH ;
ROTILIO, G .
CRC CRITICAL REVIEWS IN BIOCHEMISTRY, 1987, 22 (02) :111-180
[6]   Inhibition of mitochondrial respiration by endogenous nitric oxide:: A critical step in Fas signaling [J].
Beltrán, B ;
Quintero, M ;
García-Zaragozá, E ;
O'Connor, E ;
Esplugues, JV ;
Moncada, S .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (13) :8892-8897
[7]   Nuclear factor-kappa B and cancer: its role in prevention and therapy [J].
Bharti, AC ;
Aggarwal, BB .
BIOCHEMICAL PHARMACOLOGY, 2002, 64 (5-6) :883-888
[8]   Induction of mnsod gene by arachidonic acid is mediated by reactive oxygen species and p38 MAPK signaling pathway in human HepG2 hepatoma cells [J].
Bianchi, A ;
Bécuwe, P ;
Franck, P ;
Dauça, M .
FREE RADICAL BIOLOGY AND MEDICINE, 2002, 32 (11) :1132-1142
[9]  
BLOCK GX, 2002, AM J CLIN NUTR, V54, pA1310
[10]   DEFECTIVE GENE-EXPRESSION OF MNSOD IN CANCER-CELLS [J].
BORRELLO, S ;
DELEO, ME ;
GALEOTTI, T .
MOLECULAR ASPECTS OF MEDICINE, 1993, 14 (03) :253-258