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
  • [41] Wright A, 2002, PHOTOCHEM PHOTOBIOL, V76, P35, DOI 10.1562/0031-8655(2002)076<0035:SOMPOE>2.0.CO
  • [42] 2
  • [43] Photochemical destruction of the Bcl-2 oncoprotein during photodynamic therapy with the phthalocyanine photosensitizer Pc 4
    Xue, LY
    Chiu, SM
    Oleinick, NL
    [J]. ONCOGENE, 2001, 20 (26) : 3420 - 3427
  • [44] Yamamoto K, 1999, MOL CELL BIOL, V19, P8469