HSP70 overexpression mediates the escape of a doxorubicin-induced G2 cell cycle arrest

被引:63
作者
Karlseder, J
Wissing, D
Holzer, G
Orel, L
Sliutz, G
Auer, H
Jaattela, M
Simon, MM
机构
[1] UNIV VIENNA,BOKU,CTR APPL GENET,A-1190 VIENNA,AUSTRIA
[2] UNIV VIENNA,AKH,KLIN INNERE MED 4,DEPT OCCUPAT MED,A-1090 VIENNA,AUSTRIA
[3] DANISH CANC SOC,RES CTR,DEPT TUMOR CELL BIOL,DIV CANC BIOL,DK-2100 COPENHAGEN,DENMARK
关键词
D O I
10.1006/bbrc.1996.0373
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
The stress inducible heat shock protein 70 (hsp70) confers resistance to a variety of adverse environmental conditions including certain anticancer drugs. In the present study we explored cellular consequences of hsp70 overexpression with respect to genotoxic stress. Employing an isogenic set of stable transfectant cells, one overexpressing hsp 70 and the other serving as control, we found that a high hsp70 expression level is sufficient to provide protection against the cytotoxicity of doxorubicin. In addition, hsp70-protected cells showed the capability to restart cell proliferation at concentrations where control cells arrested. However, the DNA lesion density was comparable in the lines used. Recording the cell cycle control revealed a dramatic shortening of the doxorubicin-mediated cell cycle arrest in the G2 phase upon hsp70 overexpression. Our data suggest an involvement of hsp70 in the regulation of the cell cycle. (C) 1996 Academic Press, Inc.
引用
收藏
页码:153 / 159
页数:7
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