Abstract
The possible involvement of PKC in the regulation of heat shock genes expression was investigated with three isoquinolinesulfonamide derivatives (H-7, H-8, and HA1004) in DUT-145, MCF-7, and MCF-7/ADR cells. The drug was added 1 hr before and during heating at 41 degrees C. Northern blots show that the levels of HSP70 and HSP28 mRNA increased rapidly and reached maximal values within 4-8 hr and 8-12 hr, respectively. H-7 and H-8 which are potent PKC inhibitors selectively suppressed the accumulation of HSP70 mRNA as well as the synthesis of HSP70. In contrast, HA1004 which is a potent PKA inhibitor but a weak PKC inhibitor did not affect HSP70 gene expression. These results suggest that PKC rather than PKA plays an important role in the regulation of heat shock gene expression.
Publication types
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Research Support, Non-U.S. Gov't
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Research Support, U.S. Gov't, P.H.S.
MeSH terms
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1-(5-Isoquinolinesulfonyl)-2-Methylpiperazine
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Blotting, Northern
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Breast Neoplasms
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Cyclic AMP-Dependent Protein Kinases / antagonists & inhibitors
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Cyclic AMP-Dependent Protein Kinases / metabolism
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Female
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Gene Expression Regulation, Neoplastic / drug effects*
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Heat-Shock Proteins / biosynthesis*
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Heat-Shock Proteins / isolation & purification
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Hot Temperature
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Humans
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Isoquinolines / pharmacology*
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Kinetics
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Leucine / pharmacology
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Male
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Piperazines / pharmacology*
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Prostatic Neoplasms
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Protein Kinase C / antagonists & inhibitors
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Protein Kinase C / metabolism*
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RNA, Messenger / biosynthesis
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RNA, Messenger / metabolism
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Sulfonamides*
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Tumor Cells, Cultured
Substances
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Heat-Shock Proteins
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Isoquinolines
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Piperazines
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RNA, Messenger
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Sulfonamides
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1-(5-Isoquinolinesulfonyl)-2-Methylpiperazine
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N-(2-(methylamino)ethyl)-5-isoquinolinesulfonamide
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N-(2-guanidinoethyl)-5-isoquinolinesulfonamide
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Cyclic AMP-Dependent Protein Kinases
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Protein Kinase C
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Leucine