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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...

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Detalles Bibliográficos
Autores principales: Abe, Tetsuya, Fukamachi, Yukiyo, Kanazawa, Yohsuke, Furukawa, Hiroshi, Shimizu, Kenji, Hirano, Takeshi, Kasai, Hiroshi, Kashimura, Masamichi, Higashi, Ken
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 1996
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.
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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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