Abstract
Purpose: C-myc was studied in cyclooxygenase (COX)-2 associated granulosa cell apoptosis. Methods: Granulosa cells (N = 5 cases) were incubated for 24 h in either 1 or 50 μM COX-2 inhibitor, 1 or 50 μM COX-1/COX-2 inhibitor, negative or positive controls. Single primer polymerase chain reaction of c-myc exon 1 were performed. Bisbenzimide-stained control single-stranded (ssDNA) were hybridized to SYBR Gold-stained ssDNA and fluorescent images analyzed. Results: C-myc was disrupted by the high-dose COX-2 inhibitor. Cell viability decreased with COX-1 and COX-2 inhibition. However, cell viability was similar for the positive control and at low-dose COX-2 inhibition. Conclustion: Inhibition of both COX-1 and COX-2 initiated apoptosis without disrupting c-myc suggesting a protective effect on c-myc. The low dosage of the COX-2 inhibitor did not disrupt c-myc and cell viability. C-myc sensitization was not part of apoptosis.
| Original language | English |
|---|---|
| Pages (from-to) | 577-581 |
| Number of pages | 5 |
| Journal | Journal of Assisted Reproduction and Genetics |
| Volume | 19 |
| Issue number | 12 |
| DOIs | |
| State | Published - Dec 1 2002 |
ASJC Scopus Subject Areas
- Reproductive Medicine
- Genetics
- Obstetrics and Gynecology
- Developmental Biology
- Genetics(clinical)
Keywords
- Apoptosis
- Comparative genomic hybridization
- Cyclooxygenase COX-2
- Granulosa cells
- Prostaglandins
- Cyclooxygenase Inhibitors/pharmacology
- Exons
- Cyclooxygenase 2
- Humans
- Cyclooxygenase 1
- Cell Survival/drug effects
- Genes, myc
- Dose-Response Relationship, Drug
- Female
- Isoenzymes/antagonists & inhibitors
- Oxidants/pharmacology
- Pyrazoles
- Apoptosis/drug effects
- Cells, Cultured
- Celecoxib
- Prostaglandin-Endoperoxide Synthases/drug effects
- Membrane Proteins
- Granulosa Cells/cytology
- Cyclooxygenase 2 Inhibitors
- Sulfonamides/pharmacology
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