Multifunctional redox catalysts as selective enhancers of oxidative stress

被引:48
作者
Fry, FH
Holme, AL
Giles, NM
Giles, GI
Collins, C
Holt, K
Pariagh, S
Gelbrich, T
Hursthouse, MB
Gutowski, NJ
Jacob, C
机构
[1] Univ Exeter, Sch Biol & Chem Sci, Exeter EX4 4QD, Devon, England
[2] Univ Southampton, Sch Chem, Southampton SO17 1BJ, Hants, England
[3] Univ Exeter, Peninsula Med Sch, Exeter EX2 5DW, Devon, England
[4] Univ Plymouth, Plymouth PL4 8AA, Devon, England
[5] Royal Devon & Exeter Hosp, Exeter EX2 5DW, Devon, England
[6] Univ Saarland, Fachbereich 8 2 Pharmazeut & Med Chem, D-66041 Saarbrucken, Germany
基金
英国惠康基金;
关键词
D O I
10.1039/b502197a
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Certain cancer cells proliferate under conditions of oxidative stress (OS) and might therefore be selectively targeted by redox catalysts. Among these catalysts, compounds containing a chalcogen and a quinone redox centre are particularly well suited to respond to the presence of OS. These catalysts combine the specific electrochemical features of quinones and chalcogens. They exhibit high selectivity and efficiency against oxidatively stressed rat PC12, human Jurkat and human Daudi cells in cell culture, where their mode of action most likely involves the catalytic activation of existent and the generation of new reactive oxygen species. The high efficiency and selectivity shown by these catalysts makes them interesting for the development of anti-cancer drugs.
引用
收藏
页码:2579 / 2587
页数:9
相关论文
共 38 条
[21]   Ebselen, a selenium-containing redox drug, releases zinc from metallothionein [J].
Jacob, C ;
Maret, W ;
Vallee, BL .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1998, 248 (03) :569-573
[22]   Selenium redox biochemistry of zinc-sulfur coordination sites in proteins and enzymes [J].
Jacob, C ;
Maret, W ;
Vallee, BL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (05) :1910-1914
[23]   CULTURE OF HUMAN ENDOTHELIAL CELLS DERIVED FROM UMBILICAL VEINS - IDENTIFICATION BY MORPHOLOGIC AND IMMUNOLOGICAL CRITERIA [J].
JAFFE, EA ;
NACHMAN, RL ;
BECKER, CG ;
MINICK, CR .
JOURNAL OF CLINICAL INVESTIGATION, 1973, 52 (11) :2745-2756
[24]   Hydrogen peroxide-induced apoptosis in PC12 cells and the protective effect of puerarin [J].
Jiang, B ;
Liu, JH ;
Bao, YM ;
An, LJ .
CELL BIOLOGY INTERNATIONAL, 2003, 27 (12) :1025-1031
[25]   Selective cell death by water-soluble Fe-porphyrins with superoxide dismutase (SOD) activity [J].
Kasugai, N ;
Murase, T ;
Ohse, T ;
Nagaoka, S ;
Kawakami, H ;
Kubota, S .
JOURNAL OF INORGANIC BIOCHEMISTRY, 2002, 91 (02) :349-355
[26]  
Kearns S, 2000, ADV EXP MED BIOL, V483, P563
[27]   Increases in free radicals and cytoskeletal protein oxidation and nitration in the colon of patients with inflammatory bowel disease [J].
Keshavarzian, A ;
Banan, A ;
Farhadi, A ;
Komanduri, S ;
Mutlu, E ;
Zhang, Y ;
Fields, JZ .
GUT, 2003, 52 (05) :720-728
[28]   Oxidative stress attenuates Fas-mediated apoptosis in Jurkat T cell line through Bfl-1 induction [J].
Kim, H ;
Kim, YN ;
Kim, H ;
Kim, CW .
ONCOGENE, 2005, 24 (07) :1252-1261
[29]  
Massy ZA, 2002, J NEPHROL, V15, P336
[30]   REDOX BUFFERING ABILITY OF LYMPHOID-CELLS EVALUATED BY THE OXIDATION OF 2',7'-DICHLOROFLUORESCIN [J].
MELINO, G ;
SAVINI, I ;
GUERRIERI, P ;
FINAZZIAGRO, A .
FREE RADICAL RESEARCH COMMUNICATIONS, 1990, 11 (4-5) :213-221