Effect of mifepristone on COX-2 both in eutopic and ectopic endometrium in mouse endometriotic model
Mifepristone reduced COX-2 mRNA and protein in a mouse endometriosis model but did not alter ectopic lesion size or serum PGE2 levels.
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This paper studied the effect of the antiprogesterone mifepristone on cyclooxygenase-2 (COX-2) mRNA and protein expression in both eutopic and ectopic endometrium in a mouse endometriosis model, using 30 mice allocated to mifepristone or control groups evaluated at 1, 4, and 6 weeks. Ectopic lesion size was monitored by small animal optical imaging, while COX-2 mRNA and protein were measured by RT-PCR and western blot, and serum PGE2 was assessed by ELISA. Mifepristone did not significantly change fluorescent intensity (ectopic lesion size) at any time point, but it decreased COX-2 mRNA transcription at 1 and 4 weeks and decreased COX-2 protein at 4 and 6 weeks, with a non-significant trend toward lower serum PGE2. This paper is centrally about endometriosis—specifically, mifepristone’s impact on COX-2 and its prostaglandin product in eutopic versus ectopic endometrial tissue in a mouse endometriotic model.
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References (23)
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- Aromatase and other steroidogenic genes in endometriosis: translational aspects via openalex
- Deficient 17 -Hydroxysteroid Dehydrogenase Type 2 Expression in Endometriosis: Failure to Metabolize 17 -Estradiol via openalex
- Deficient 17β-Hydroxysteroid Dehydrogenase Type 2 Expression in Endometriosis: Failure to Metabolize 17β-Estradiol<sup>1</sup> via openalex
- Development of an experimental model of endometriosis using mice that ubiquitously express green fluorescent protein via openalex
- Distribution of cyclooxygenase-2 in eutopic and ectopic endometrium in endometriosis and adenomyosis via openalex
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Cited by (4)
- Investigation of the 12-month efficacy and safety of low-dose mifepristone in the treatment of painful adenomyosis 2022
- Gestagens in the treatment of endometriosis 2018
- A high level of TGF-B1 promotes endometriosis development via cell migration, adhesiveness, colonization, and invasiveness† 2018
- Gestagens in the treatment of endometriosis 2018
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