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Matrix metalloproteinases and endometriosis
Kevin G Osteen1, Grant R Yeaman, Kaylon L Bruner-Tran
1Women's Reproductive Health Research Center, Department of Obstetrics Gynecology, Vanderbilt University School of Medicine, B-1100 Medical Center North, Nashville, TN 37232, USA.
Seminars in Reproductive Medicine
|August 15, 2003
Summary
Endometriosis affects 10-20% of women, likely due to factors beyond retrograde menstruation. Matrix metalloproteinases (MMPs) and steroid sensitivity may play key roles in disease development.
Area of Science:
- Reproductive biology
- Molecular endocrinology
- Gynecologic pathology
Background:
- Retrograde menstruation is a leading theory for endometriosis.
- However, only 10-20% of women with retrograde menstruation develop endometriosis.
- This suggests additional contributing factors are involved.
Purpose of the Study:
- To explore the factors differentiating women who develop endometriosis from those who do not.
- To investigate the role of matrix metalloproteinases (MMPs) and steroid sensitivity in endometriosis pathogenesis.
Main Methods:
- The study reviews existing literature on endometriosis development.
- It focuses on the potential roles of steroid exposure, immune factors, genetics, environmental toxins, and MMPs.
- Progesterone sensitivity and MMP expression in the endometrium are examined.
Main Results:
- Matrix metalloproteinases (MMPs) are implicated in the invasive establishment of endometriosis.
- Women with endometriosis exhibit altered MMP expression and reduced progesterone sensitivity.
- These alterations may link refluxed endometrium to disease development in susceptible individuals.
Conclusions:
- Factors beyond retrograde menstruation, including steroid exposure, immunology, genetics, and environmental toxins, are crucial for endometriosis development.
- Altered endometrial matrix metalloproteinase (MMP) expression and progesterone resistance are key mechanisms.
- These factors explain why only a subset of women with retrograde menstruation develop endometriosis.