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Cyclooxygenase (COX)-2 and granulosa cell apoptosis in vitro

  • Angela S. Caffrey
  • , William C. Patton
  • , Johannah U. Corselli
  • , Ron E. Swensen
  • , Alan King
  • , Philip J. Chan

Research output: Contribution to journalArticlepeer-review

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 languageEnglish
Pages (from-to)577-581
Number of pages5
JournalJournal of Assisted Reproduction and Genetics
Volume19
Issue number12
DOIs
StatePublished - 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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