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Inhibition of Nucleolar Function and Morphological Change by Adriamycin Associated with Heat Shock Protein 70 Accumulation
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 consid...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Blackwell Publishing Ltd
1996
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5921194/ https://www.ncbi.nlm.nih.gov/pubmed/8878457 http://dx.doi.org/10.1111/j.1349-7006.1996.tb02124.x |
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author | Abe, Tetsuya Fukamachi, Yukiyo Kanazawa, Yohsuke Furukawa, Hiroshi Shimizu, Kenji Hirano, Takeshi Kasai, Hiroshi Kashimura, Masamichi Higashi, Ken |
author_facet | Abe, Tetsuya Fukamachi, Yukiyo Kanazawa, Yohsuke Furukawa, Hiroshi Shimizu, Kenji Hirano, Takeshi Kasai, Hiroshi Kashimura, Masamichi Higashi, Ken |
author_sort | Abe, Tetsuya |
collection | PubMed |
description | 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 μM 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. |
format | Online Article Text |
id | pubmed-5921194 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1996 |
publisher | Blackwell Publishing Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-59211942018-05-11 Inhibition of Nucleolar Function and Morphological Change by Adriamycin Associated with Heat Shock Protein 70 Accumulation Abe, Tetsuya Fukamachi, Yukiyo Kanazawa, Yohsuke Furukawa, Hiroshi Shimizu, Kenji Hirano, Takeshi Kasai, Hiroshi Kashimura, Masamichi Higashi, Ken Jpn J Cancer Res Article 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 μM 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. Blackwell Publishing Ltd 1996-09 /pmc/articles/PMC5921194/ /pubmed/8878457 http://dx.doi.org/10.1111/j.1349-7006.1996.tb02124.x Text en |
spellingShingle | Article Abe, Tetsuya Fukamachi, Yukiyo Kanazawa, Yohsuke Furukawa, Hiroshi Shimizu, Kenji Hirano, Takeshi Kasai, Hiroshi Kashimura, Masamichi Higashi, Ken Inhibition of Nucleolar Function and Morphological Change by Adriamycin Associated with Heat Shock Protein 70 Accumulation |
title | Inhibition of Nucleolar Function and Morphological Change by Adriamycin Associated with Heat Shock Protein 70 Accumulation |
title_full | Inhibition of Nucleolar Function and Morphological Change by Adriamycin Associated with Heat Shock Protein 70 Accumulation |
title_fullStr | Inhibition of Nucleolar Function and Morphological Change by Adriamycin Associated with Heat Shock Protein 70 Accumulation |
title_full_unstemmed | Inhibition of Nucleolar Function and Morphological Change by Adriamycin Associated with Heat Shock Protein 70 Accumulation |
title_short | Inhibition of Nucleolar Function and Morphological Change by Adriamycin Associated with Heat Shock Protein 70 Accumulation |
title_sort | inhibition of nucleolar function and morphological change by adriamycin associated with heat shock protein 70 accumulation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5921194/ https://www.ncbi.nlm.nih.gov/pubmed/8878457 http://dx.doi.org/10.1111/j.1349-7006.1996.tb02124.x |
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