Abstract |
We studied the effect of isoquinolinesulfonamide derivatives (H-7, H-8, and HA1004) on the expression of two heat shock genes (alpha beta-crystallin and hsp70) in NIH 3T3 and Swiss 3T3 cells after heat shock at 45 degrees for 10 min. Western blots and northern blots showed that H-7 effectively suppressed the accumulation of HSP70 and alpha B-crystallin mRNA as well as the synthesis of their proteins. The degree of suppression was dependent upon the concentration of the drug. Moreover, the expression of the hsp genes was differentially suppressed by H-7. The expression of the alpha B-crystallin gene was more effectively inhibited than that of the hsp70 gene by H-7. Nuclear run-on assay demonstrates that this difference was due to the differential effect of H-7 on the elongation of transcription of different hsp genes.
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Authors | Y J Lee, C M Berns, S Galoforo, G Erdos, J M Cho, P M Corry |
Journal | Biochemical pharmacology
(Biochem Pharmacol)
Vol. 50
Issue 8
Pg. 1149-55
(Oct 12 1995)
ISSN: 0006-2952 [Print] England |
PMID | 7488228
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, P.H.S.)
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Chemical References |
- Crystallins
- Enzyme Inhibitors
- HSP70 Heat-Shock Proteins
- Isoquinolines
- Piperazines
- RNA, Messenger
- Sulfonamides
- 1-(5-Isoquinolinesulfonyl)-2-Methylpiperazine
- N-(2-guanidinoethyl)-5-isoquinolinesulfonamide
- Protein Kinase C
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Topics |
- 1-(5-Isoquinolinesulfonyl)-2-Methylpiperazine
- 3T3 Cells
- Animals
- Base Sequence
- Cell Line
- Crystallins
(biosynthesis, genetics)
- Enzyme Inhibitors
(pharmacology)
- Gene Expression
(drug effects)
- HSP70 Heat-Shock Proteins
(biosynthesis, genetics)
- Isoquinolines
(pharmacology)
- Mice
- Molecular Sequence Data
- Piperazines
(pharmacology)
- Protein Kinase C
(antagonists & inhibitors)
- RNA, Messenger
(biosynthesis)
- Sulfonamides
- Transcription, Genetic
(drug effects)
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