Aldo-keto reductases AKR1C1, AKR1C2 and AKR1C3 may enhance progesterone metabolism in ovarian endometriosis
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This study investigated how aldo-keto reductases AKR1C1, AKR1C2, and AKR1C3 might influence progesterone metabolism within ovarian endometriosis.
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Cited by (16)
- The effect of androgens on the risk of endometriosis sub-phenotypes and ovarian neoplasms: A Mendelian randomization study 2024
- Applying a computational transcriptomics-based drug repositioning pipeline to identify therapeutic candidates for endometriosis 2022
- Is intracrinology of endometriosis relevant in clinical practice? A systematic review on estrogen metabolism 2022
- Emerging hallmarks of endometriosis metabolism: A promising target for the treatment of endometriosis 2022
- Aldo-keto reductase 1C3—Assessment as a new target for the treatment of endometriosis 2019
- Is it time for a paradigm shift in drug research and development in endometriosis/adenomyosis? 2018
- SULFATION PATHWAYS: Contribution of intracrine oestrogens to the aetiology of endometriosis 2018
- Phospholipase A2 group IIA is elevated in endometriomas but not in peritoneal fluid and serum of ovarian endometriosis patients 2014
- Expression of AKR1B1, AKR1C3 and other genes of prostaglandin F2α biosynthesis and action in ovarian endometriosis tissue and in model cell lines 2014
- Identification of multiple and distinct defects in prostaglandin biosynthetic pathways in eutopic and ectopic endometrium of women with endometriosis 2013
- Disturbed balance between phase I and II metabolizing enzymes in ovarian endometriosis: A source of excessive hydroxy-estrogens and ROS? 2012
- Effects of progestins on local estradiol biosynthesis and action in the Z-12 endometriotic epithelial cell line 2012
- Progestin effects on expression of AKR1C1–AKR1C3, SRD5A1 and PGR in the Z-12 endometriotic epithelial cell line 2012
- Enzymes of the AKR1B and AKR1C Subfamilies and Uterine Diseases 2012
- Medical Treatment in Endometriosis 2012
- Expression of human aldo-keto reductase 1C2 in cell lines of peritoneal endometriosis: Potential implications in metabolism of progesterone and dydrogesterone and inhibition by progestins 2012
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