Abstract |
Delta12-prostaglandin (PG)J2, which has been reported to have potent growth inhibitory activity in various tumor cells, induced apoptosis at 5 microg/ml culture medium in transformed mouse endothelial (F2) cells. Immunoblot analysis using anti-p53 or anti-WAF1 antibodies demonstrated that these two proteins had increased following delta12-PGJ2 treatment in F2 cells. Western blotting analysis using anti-heme oxygenase-1 (heat shock protein (HSP)32) antibody also revealed that delta12-PGJ2 induced HSP32 formation in F2 cells. HSP32 was also induced by heat shock treatment at 43 degrees C for 90 min. In contrast, HSP72 was not induced by heat shock or by delta12-PGJ2 treatment. In agreement with these findings, HSP32 immunofluorescence in the cytoplasm of F2 cells was intensified by delta12-PGJ2 treatment. More intense HSP32 immunoreactivity was similarly observed after heat shock treatment. These results suggest that delta12-PGJ2 caused the apoptotic cell death of F2 cells, which involved a certain process required for p53 or HSP32 induction.
|
Authors | K Ikai, H Kudo, K Toda, M Fukushima |
Journal | Prostaglandins, leukotrienes, and essential fatty acids
(Prostaglandins Leukot Essent Fatty Acids)
Vol. 58
Issue 4
Pg. 295-300
(Apr 1998)
ISSN: 0952-3278 [Print] Scotland |
PMID | 9654403
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
|
Chemical References |
- Antineoplastic Agents
- Heat-Shock Proteins
- Tumor Suppressor Protein p53
- 9-deoxy-delta-9-prostaglandin D2
- Oxygenases
- Heme Oxygenase (Decyclizing)
- Heme Oxygenase-1
- Hmox1 protein, rat
- Prostaglandin D2
|
Topics |
- Animals
- Antineoplastic Agents
(pharmacology)
- Apoptosis
(drug effects)
- Blotting, Western
- Cell Line
- Cell Line, Transformed
(cytology, drug effects, metabolism)
- DNA Fragmentation
(drug effects)
- Endothelium, Vascular
(cytology, drug effects, metabolism)
- Fluorescent Antibody Technique, Direct
- Heat-Shock Proteins
(drug effects, immunology, metabolism)
- Heme Oxygenase (Decyclizing)
(drug effects, metabolism)
- Heme Oxygenase-1
- Oxygenases
- Prostaglandin D2
(analogs & derivatives, pharmacology)
- Tumor Suppressor Protein p53
(drug effects, metabolism)
|