Cell death and growth arrest in response to photodynamic therapy with membrane-bound photosensitizers

被引:117
作者
Piette, J [1 ]
Volanti, C
Vantieghem, A
Matroule, JY
Habraken, Y
Agostinis, P
机构
[1] Univ Liege, Inst Pathol B23, Lab Virol & Immunol, B-4000 Liege, Belgium
[2] Catholic Univ Louvain, Div Biochem, B-3000 Louvain, Belgium
关键词
photodynamic therapy; photosensitizer; apoptosis; mitochondria; Bcl-2;
D O I
10.1016/S0006-2952(03)00539-2
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Photodynamic therapy (PDT) is a treatment for cancer and for certain benign conditions that is based on the use of a photosensitizer and light to produce reactive oxygen species in cells. Many of the photosensitizers currently used in PDT localize in different cell compartments such as mitochondria, lysosomes, endoplasmic reticulum and generate cell death by triggering necrosis and/or apoptosis. Efficient cell death is observed when light, oxygen and the photosensitizer are not limiting ("high dose PDT"). When one of these components is limiting ("low dose PDT"), most of the cells do not immediately undergo apoptosis or necrosis but are growth arrested with several transduction pathways activated. This commentary will review the mechanism of apoptosis and growth arrest mediated by two important PDT agents. i.e. pyropheophorbide and hypericin. (C) 2003 Elsevier Inc. All rights reserved.
引用
收藏
页码:1651 / 1659
页数:9
相关论文
共 44 条
[1]   Hypericin in cancer treatment: more light on the way [J].
Agostinis, P ;
Vantieghem, A ;
Merlevede, W ;
de Witte, PAM .
INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY, 2002, 34 (03) :221-241
[2]   NF-κB activation in cancer:: a challenge for ubiquitination- and proteasome-based therapeutic approach [J].
Amit, S ;
Ben-Neriah, Y .
SEMINARS IN CANCER BIOLOGY, 2003, 13 (01) :15-28
[3]   The activation of the c-Jun N-terminal kinase and p38 mitogen-activated protein kinase signaling pathways protects HeLa cells from apoptosis following photodynamic therapy with hypericin [J].
Assefa, Z ;
Vantieghem, A ;
Declercq, W ;
Vandenabeele, P ;
Vandenheede, JR ;
Merlevede, W ;
de Witte, P ;
Agostinis, P .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (13) :8788-8796
[4]   Unwinding the loop of Bcl-2 phosphorylation [J].
Blagosklonny, MV .
LEUKEMIA, 2001, 15 (06) :869-874
[5]   Mediators of peripheral blood neutrophilia induced by photodynamic therapy of solid tumors [J].
Cecic, I ;
Korbelik, M .
CANCER LETTERS, 2002, 183 (01) :43-51
[6]   Phthalocyanine 4 photodynamic therapy-induced apoptosis of mouse L5178Y-R cells results from a delayed but extensive release of cytochrome c from mitochondria [J].
Chiu, SM ;
Evans, HH ;
Lam, M ;
Nieminen, AL ;
Oleinick, NL .
CANCER LETTERS, 2001, 165 (01) :51-58
[7]   Novel role for JNK as a stress-activated Bcl2 kinase [J].
Deng, XM ;
Xiao, L ;
Lang, WH ;
Gao, FQ ;
Ruvolo, P ;
May, WS .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (26) :23681-23688
[8]   All along the watchtower: on the regulation of apoptosis regulators [J].
Fadeel, B ;
Zhivotovsky, B ;
Orrenius, S .
FASEB JOURNAL, 1999, 13 (13) :1647-1657
[9]   Missing pieces in the NF-κB puzzle [J].
Ghosh, S ;
Karin, M .
CELL, 2002, 109 :S81-S96
[10]  
Girotti AW, 1998, J LIPID RES, V39, P1529