Involvement of DNA-dependent protein kinase in regulation of the mitochondrial heat shock proteins

被引:19
作者
Um, JH
Kang, CD
Hwang, BW
Ha, MY
Hur, JG
Kim, DW
Chung, BS
Kim, SH [1 ]
机构
[1] Pusan Natl Univ, Coll Med, Dept Biochem, Pusan 602739, South Korea
[2] Pusan Natl Univ, Coll Med, Res Ctr Mol Med, Pusan 602739, South Korea
[3] Chang Won Natl Univ, Coll Nat Sci, Dept Microbiol, Chang Won 641773, South Korea
基金
新加坡国家研究基金会;
关键词
mitochondrial heat shock; mitochondrial heat shock protein; multidrug-resistant; anti-apoptotic function;
D O I
10.1016/S0145-2126(02)00264-3
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Since DNA-dependent protein kinase (DNA-PK) has been known to play a protective role against drug-induced apoptosis, the role of DNA-PK in the regulation of mitochondrial heat shock proteins by anticancer drugs was examined. The levels of basal and drug-induced mitochondrial heat shock proteins of drug-sensitive parental cells were higher than those of multidrug-resistant (MDR) cells. We also demonstrated that the development of MDR might be correlated with the increased expression of Ku-subunit of DNA-PK and concurrent down-regulation of mitochondrial heat shock proteins. The basal mtHsp70 and Hsp60 levels of Ku70(-/-) cells, which were known to be sensitive to anticancer drugs, were higher than those of parental MEF cells, but conversely these mitochondrial heat shock proteins of R7080-6 cells over-expressing both Ku70 and Ku80 were lower than those of parental Rat-1 cells. Also, the mtHsp70 and Hsp60 levels of DNA-PKcs-deficient SCID cells were higher than those of parental CB-17 cells. Our results suggest the possibility that mitochondrial heat shock protein may be one of determinants of drug sensitivity and could be regulated by DNA-PK activity. (C) 2003 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:509 / 516
页数:8
相关论文
共 58 条
[1]   THE EFFECT OF CYCLIC-AMP ON THE REGULATION OF C-MYC EXPRESSION IN T-LYMPHOMA-CELLS [J].
ALBERT, DA .
JOURNAL OF CLINICAL INVESTIGATION, 1995, 95 (04) :1490-1496
[2]  
BECK WT, 1979, CANCER RES, V39, P2070
[3]   Heat shock protein 72 modulates pathways of stress-induced apoptosis [J].
Buzzard, KA ;
Giaccia, AJ ;
Killender, M ;
Anderson, RL .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (27) :17147-17153
[4]  
CIOCCA DR, 1992, CANCER RES, V52, P3648
[5]   HEAT-SHOCK PROTEIN-HSP70 IN PATIENTS WITH AXILLARY LYMPH NODE-NEGATIVE BREAST-CANCER - PROGNOSTIC IMPLICATIONS [J].
CIOCCA, DR ;
CLARK, GM ;
TANDON, AK ;
FUQUA, SAW ;
WELCH, WJ ;
MCGUIRE, WL .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1993, 85 (07) :570-574
[6]   BIOLOGICAL AND CLINICAL IMPLICATIONS OF HEAT-SHOCK PROTEIN 27000 (HSP27) - A REVIEW [J].
CIOCCA, DR ;
OESTERREICH, S ;
CHAMNESS, GC ;
MCGUIRE, WL ;
FUQUA, SAW .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1993, 85 (19) :1558-1570
[7]   HEAT-SHOCK PROTEINS AND MOLECULAR CHAPERONES - MEDIATORS OF PROTEIN CONFORMATION AND TURNOVER IN THE CELL [J].
CRAIG, EA ;
WEISSMAN, JS ;
HORWICH, AL .
CELL, 1994, 78 (03) :365-372
[8]  
Creagh EM, 1999, IMMUNOLOGY, V97, P36
[9]  
Cvijic ME, 1997, CELL GROWTH DIFFER, V8, P1243
[10]  
DIX DJ, 1996, P NATL ACAD SCI USA, V93, P3648