The Potential of Zn(II) N-Alkylpyridylporphyrins for Anticancer Therapy

被引:22
作者
Benov, Ludmil [1 ]
Craik, James [1 ]
Batinic-Haberle, Ines [2 ]
机构
[1] Kuwait Univ, Dept Biochem, Fac Med, Safat 13110, Kuwait
[2] Duke Univ, Med Ctr, Dept Radiat Oncol, Durham, NC 27710 USA
关键词
Ortho; meta; and para isomeric Zn(II) N-alkylpyridylporphyrins; photosensitizer; singlet oxygen; photodynamic therapy; PHOTODYNAMIC THERAPY; SUBCELLULAR-LOCALIZATION; SINGLET OXYGEN; CATIONIC PORPHYRINS; SOD MIMICS; SIGNALING PATHWAYS; PHOTO-TREATMENT; FREE-RADICALS; TUMOR-CELLS; IN-VITRO;
D O I
10.2174/187152011795255975
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Reactive oxygen species (ROS) are considered to be a main cause for cancer development, but they can also be used for cancer eradication. Because of this dual nature of ROS action, both antioxidant and prooxidant therapeutic agents have been developed and some have shown clinical promise. Selective uptake of porphyrins by malignant cells has for a long time been used for tumor imaging and for targeted delivery of ROS. Redox-active Mn porphyrins can act both as antioxidants and as prooxidants, and may thus be used in anticancer therapy. Porphyrins, which chelate redox inactive metals, for example Zn, demonstrate photo-sensitizing activity and thus can produce singlet oxygen and other reactive oxygen species in cancer cells on irradiation with visible light. Here we review the properties of Zn(II) N-alkylpyridylporphyrin-based photosensitizers, and their ability to damage selected cellular targets.
引用
收藏
页码:233 / 241
页数:9
相关论文
共 114 条
[31]   Signaling Functions of Reactive Oxygen Species [J].
Forman, Henry Jay ;
Maiorino, Matilde ;
Ursini, Fulvio .
BIOCHEMISTRY, 2010, 49 (05) :835-842
[32]  
Frank J, 1998, CANCER RES, V58, P2693
[33]   Genotoxic potential of porphyrin type photosensitizers with particular emphasis on 5-aminolevulinic acid: Implications for clinical photodynamic therapy [J].
Fuchs, J ;
Weber, S ;
Kaufmann, R .
FREE RADICAL BIOLOGY AND MEDICINE, 2000, 28 (04) :537-548
[34]   Binding of the Mn(III) complex of meso-tetrakis(4-N-methyl-pyridiniumyl)porphyrin to DNA.: Effect of ionic strength [J].
Gandini, SCM ;
Yushmanov, VE ;
Perussi, JR ;
Tabak, M ;
Borissevitch, IE .
JOURNAL OF INORGANIC BIOCHEMISTRY, 1999, 73 (1-2) :35-40
[35]   MEASUREMENT OF THE RATE OF UPTAKE AND SUBCELLULAR-LOCALIZATION OF PORPHYRINS IN CELLS USING FLUORESCENCE DIGITAL IMAGING MICROSCOPY [J].
GEORGIOU, GN ;
AHMET, MT ;
HOULTON, A ;
SILVER, J ;
CHERRY, RJ .
PHOTOCHEMISTRY AND PHOTOBIOLOGY, 1994, 59 (04) :419-422
[36]  
GOLLNICK S, 2003, CRC HDB ORGANIC PHOT, P1
[37]   Redox metabolism and malignancy [J].
Grek, Christina L. ;
Tew, Kenneth D. .
CURRENT OPINION IN PHARMACOLOGY, 2010, 10 (04) :362-368
[38]  
Halliwell B, 1996, ANNU REV NUTR, V16, P33, DOI 10.1146/annurev.nu.16.070196.000341
[39]   Photodynamic therapy: a new antimicrobial approach to infectious disease? [J].
Hamblin, MR ;
Hasan, T .
PHOTOCHEMICAL & PHOTOBIOLOGICAL SCIENCES, 2004, 3 (05) :436-450
[40]   HOW DOES PHOTODYNAMIC THERAPY WORK [J].
HENDERSON, BW ;
DOUGHERTY, TJ .
PHOTOCHEMISTRY AND PHOTOBIOLOGY, 1992, 55 (01) :145-157