Inhibition of nucleolar function and morphological change by adriamycin associated with heat shock protein 70 accumulation

被引:15
作者
Abe, T
Fukamachi, Y
Kanazawa, Y
Furukawa, H
Shimizu, K
Hirano, T
Kasai, H
Kashimura, M
Higashi, K
机构
[1] UNIV OCCUPAT & ENVIRONM HLTH,SCH MED,DEPT BIOCHEM,YAHATANISHI KU,KITAKYUSHU,FUKUOKA 807,JAPAN
[2] UNIV OCCUPAT & ENVIRONM HLTH,SCH MED,DEPT ANAT,YAHATANISHI KU,KITAKYUSHU,FUKUOKA 807,JAPAN
[3] UNIV OCCUPAT & ENVIRONM HLTH,SCH MED,DEPT OBSTET & GYNECOL,YAHATANISHI KU,KITAKYUSHU,FUKUOKA 807,JAPAN
[4] UNIV OCCUPAT & ENVIRONM HLTH,DEPT ENVIRONM ONCOL,INST IND ECOL,YAHATANISHI KU,KITAKYUSHU,FUKUOKA 807,JAPAN
来源
JAPANESE JOURNAL OF CANCER RESEARCH | 1996年 / 87卷 / 09期
关键词
adriamycin; HSP70; nucleolus; DNA damage; HeLa cells;
D O I
10.1111/j.1349-7006.1996.tb02124.x
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Adriamycin (ADR) has been considered to target mainly DNA metabolism in the nucleus. Recently, we observed the nuclear translocation of heat shock protein 70 (HSP70) after ADR treatment. We examined which intranuclear changes might be related to this alteration of HSP70 localization. We found considerable alternations in the nucleolar morphology and function in ADR-treated tumor cells, i.e., a ring-shaped segregation of granular components of almost all nucleoli and a dramatic reduction of nucleolar 45S ribosomal precursor RNA biosynthesis in HeLa cells exposed to 100 mu M ADR for 2 h. Concomitantly with these changes, HSP70 was concentrated into the nucleoli, as in the case of heat shock treatment. These results indicate a novel anticancer effect of ADR via the suppression of cellular protein biosynthesis, in addition to its effect on DNA.
引用
收藏
页码:945 / 951
页数:7
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