TY - JOUR
T1 - Cyclooxygenase (COX)-2 and granulosa cell apoptosis in vitro
AU - Caffrey, Angela S.
AU - Patton, William C.
AU - Corselli, Johannah U.
AU - Swensen, Ron E.
AU - King, Alan
AU - Chan, Philip J.
N1 - 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 microM COX-2 inhibitor, 1 or 50 microM COX-1/COX-2 inhibitor, negative or positive controls Single primer polymerase chain reaction of c-myc exon 1 were performed.
PY - 2002/12/1
Y1 - 2002/12/1
N2 - 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.
AB - 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.
KW - Apoptosis
KW - Comparative genomic hybridization
KW - Cyclooxygenase COX-2
KW - Granulosa cells
KW - Prostaglandins
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U2 - 10.1023/A:1021215216246
DO - 10.1023/A:1021215216246
M3 - Article
C2 - 12503890
SN - 1058-0468
VL - 19
SP - 577
EP - 581
JO - Journal of Assisted Reproduction and Genetics
JF - Journal of Assisted Reproduction and Genetics
IS - 12
ER -