Involvement of c-Jun NH2-terminal kinase pathway in differential regulation of heat shock proteins by anticancer drugs Journal Article


Authors: Kim, S. H.; Kim, D.; Jung, G. S.; Um, J. H.; Chung, B. S.; Kang, C. D.
Article Title: Involvement of c-Jun NH2-terminal kinase pathway in differential regulation of heat shock proteins by anticancer drugs
Abstract: In the present study, we examined the modulation of heat shock factor 1 (HSF1) activity and expression of heat shock proteins (HSPs) after exposure to anticancer drugs. Anticancer drugs induced HSF1 DNA-binding activity, and this was followed by an increase of mitochondrial HSP75 and HSP60 levels and concurrent decrease of cytoplasmic HSP70 levels. Unlike heat shock-induced full phosphorylation, HSF1 was partially phosphorylated after exposure to vincristine, and this result was tightly correlated with the kinetics of JNK/SAPK activation, and up-regulation of mitochondrial HSP75 level and concurrent down-regulation of HSP70. Furthermore, the dominant-negative mutant of SEK1 blocked the phosphorylation of HSF1 and up-regulation of mitochondrial HSP75 in response to vincristine or vinblastine. These data suggest that anticancer drugs regulate the HSF1 transcriptional activity differently from heat shock, and JNK/SAPK pathway appears to be involved in anticancer drug-induced HSF1 phosphorylation and consequently differential regulation of mitochondrial HSP75 and HSP60 and cytoplasmic HSP70.
Keywords: controlled study; protein expression; protein phosphorylation; human cell; nonhuman; antineoplastic agent; animal cell; mouse; stress activated protein kinase; vincristine; vinblastine; animalia; transcription regulation; cytoplasm; dna binding; mitochondrion; heat shock protein; human; priority journal; article
Journal Title: Biochemical and Biophysical Research Communications
Volume: 262
Issue: 2
ISSN: 0006-291X
Publisher: Elsevier Science, Inc.  
Date Published: 1999-08-27
Start Page: 516
End Page: 522
Language: English
DOI: 10.1006/bbrc.1999.1229
PUBMED: 10462506
PROVIDER: scopus
DOI/URL:
Notes: Article -- Export Date: 16 August 2016 -- Source: Scopus
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  1. Dooha Kim
    21 Kim