Induction of Hsp60 by photofrin-mediated photodynamic therapy

被引:50
作者
Hanlon, JG
Adams, K
Rainbow, AJ
Gupta, RS
Singh, G
机构
[1] Hamilton Reg Canc Ctr, Hamilton, ON L8V 5C2, Canada
[2] McMaster Univ, Dept Biol, Hamilton, ON L8V 2C5, Canada
[3] McMaster Univ, Dept Biochem, Hamilton, ON L8V 2C5, Canada
[4] McMaster Univ, Dept Pathol & Mol Med, Hamilton, ON L8V 2C5, Canada
关键词
PDT; Photofrin II (R); heat shock proteins; Hsp60;
D O I
10.1016/S1011-1344(01)00189-0
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
Photodynamic therapy (PDT) invokes a number of cellular responses. Other studies have shown that PDT induces transcription and translation of heat shock proteins (Hsps). The expression of mitochondrial heat shock protein, Hsp60, was measured following in vitro Photofrin-mediated PDT in the colon cancer cell line HT29 and its PDT-induced resistant variant HT29-P14 as well as the radiation-induced fibrosarcoma cells RIF-I and its PDT-induced resistant variant, RIF-8A. Basal levels of Hsp60 were found to be similar in the two murine cell lines. In the human model, the resistant HT29-P14 cell line showed a small increase in basal levels relative to its parental population. Incubation with Photofrin (R) (PH) alone or photosensitization caused a significant increase in Hsp60 levels in all cell lines as determined by flow cytometry. A dose-dependent and temporal relationship for PDT response was observed, maximum levels were detected 6-8 h post PDT, at which time, Hsp60 induction was found to be significantly greater in the two resistant variants. Induction in the RIF cells was also found to be greater after incubation with PH alone at the highest doses tested. These results indicate that the presence of PH and the subsequent oxidative stress of PDT can induce Hsp60 and implicated it as a common factor that may contribute to the resistance observed in the induced resistant cells. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:55 / 61
页数:7
相关论文
共 34 条
[1]   Folding and unfolding of delta-aminolevulinic acid dehydratase and porphobilinogen deaminase induced by Uro- and protoporphyrin [J].
Afonso, SG ;
DeSalamanca, RE ;
Batlle, A .
INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY, 1997, 29 (03) :493-503
[2]   The photodynamic and non-photodynamic actions of porphyrins [J].
Afonso, SG ;
de Salamanca, RE ;
Batlle, AMD .
BRAZILIAN JOURNAL OF MEDICAL AND BIOLOGICAL RESEARCH, 1999, 32 (03) :255-266
[3]   ANALYSIS OF HEAT-SHOCK PROTEIN EXPRESSION IN MYELOID-LEUKEMIA CELLS BY FLOW-CYTOMETRY [J].
CHANT, ID ;
ROSE, PE ;
MORRIS, AG .
BRITISH JOURNAL OF HAEMATOLOGY, 1995, 90 (01) :163-168
[4]   STRESS PROTEIN EXPRESSION IN MURINE TUMOR-CELLS FOLLOWING PHOTODYNAMIC THERAPY WITH BENZOPORPHYRIN DERIVATIVE [J].
CURRY, PM ;
LEVY, JG .
PHOTOCHEMISTRY AND PHOTOBIOLOGY, 1993, 58 (03) :374-379
[5]  
DOUGHERTY TJ, 1976, CANCER RES, V36, P2330
[6]   THE GENERAL CONCEPT OF MOLECULAR CHAPERONES [J].
ELLIS, RJ .
PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY OF LONDON SERIES B-BIOLOGICAL SCIENCES, 1993, 339 (1289) :257-261
[7]   ADRIAMYCIN RESISTANCE IN CHINESE-HAMSTER FIBROBLASTS FOLLOWING OXIDATIVE STRESS-INDUCED BY PHOTODYNAMIC THERAPY [J].
FISHER, AMR ;
FERRARIO, A ;
GOMER, CJ .
PHOTOCHEMISTRY AND PHOTOBIOLOGY, 1993, 58 (04) :581-588
[8]  
GOMER CJ, 1991, CANCER RES, V51, P6574
[9]  
Gomer CJ, 1996, CANCER RES, V56, P2355
[10]   INCREASED TRANSCRIPTION AND TRANSLATION OF HEME OXYGENASE IN CHINESE-HAMSTER FIBROBLASTS FOLLOWING PHOTODYNAMIC STRESS OR PHOTOFRIN-II INCUBATION [J].
GOMER, CJ ;
LUNA, M ;
FERRARIO, A ;
RUCKER, N .
PHOTOCHEMISTRY AND PHOTOBIOLOGY, 1991, 53 (02) :275-279