Down-regulation of topoisomerase IIα is caused by up-regulation of GRP78

被引:23
作者
Gosky, D [1 ]
Chatterjee, S [1 ]
机构
[1] Case Western Reserve Univ, Canc Res Ctr, Dept Med, Div Hematol Oncol, Cleveland, OH 44106 USA
关键词
GRP78; topo II alpha; PARP1; 6-atninonicotinamide; 2-deoxyglucose; VP-16; resistance;
D O I
10.1016/S0006-291X(02)02857-7
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
Glucose-regulated protein of M-r 78 kDa (GRP78) is a resident protein of endoplasmic reticulum (ER). We have previously shown that the cells become resistant to topoisomerase IIalpha (topo IIalpha) targeted cancer chemotherapeutic drug such as etoposide (VP-16) when GRP78 is up-regulated by various means. Up-regulation of GRP78 in V79 Chinese hamster cell lines was achieved by treating the cells with NAD antagonist 6-aminonicotinamide (6AN), inhibitor of glucose metabolism such as 2-deoxyglucose (2dG). Further, up-regulation of GRP78 was also observed in V79-derived cell lines which are deficient in poly(ADP-ribose) polymerase (PARP1) metabolism. However, mechanisms of association of GRP78 up-regulation and resistance to VP-16 remained obscured under the conditions outlined above. In the manuscript. using various methods, we demonstrate, for the first time, that up-regulation of GRP78, using approaches depicted above. causes down-regulation of topo IIa and its activity. We have also discussed the clinical implications of our findings. (C) 2002 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:327 / 332
页数:6
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