Abstract | OBJECTIVE: STUDY DESIGN: RESULTS: MMP-3 was secreted in high concentrations, moderate concentrations were seen for MMP-1 and MMP-2, and very low concentrations for MMP-9. Substantially more TIMP-1 than TIMP-2 was secreted. MMP-1 and MMP-3 were uniformly attenuated by R5020, while MMP-2 was not influenced by hormone treatment. MMP-3 was upregulated by TNF-alpha in all samples while IL-1 only increased secretion in cells from endometriosis patients. CONCLUSION: The upregulation of MMP-3 by IL-1 may contribute to an increased invasiveness of uterine endometrial fragments in endometriosis patients.
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Authors | M Sillem, S Prifti, A Koch, M Neher, J Jauckus, B Runnebaum |
Journal | European journal of obstetrics, gynecology, and reproductive biology
(Eur J Obstet Gynecol Reprod Biol)
Vol. 95
Issue 2
Pg. 167-74
(Apr 2001)
ISSN: 0301-2115 [Print] Ireland |
PMID | 11301163
(Publication Type: Journal Article)
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Chemical References |
- Interleukin-1
- Tissue Inhibitor of Metalloproteinase-1
- Tissue Inhibitor of Metalloproteinases
- Tumor Necrosis Factor-alpha
- Tissue Inhibitor of Metalloproteinase-2
- Diethylstilbestrol
- Promegestone
- Matrix Metalloproteinases
- Matrix Metalloproteinase 3
- Matrix Metalloproteinase 2
- Matrix Metalloproteinase 9
- Matrix Metalloproteinase 1
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Topics |
- Adult
- Cells, Cultured
- Diethylstilbestrol
(pharmacology)
- Endometriosis
(enzymology)
- Endometrium
(enzymology)
- Female
- Humans
- Interleukin-1
(pharmacology)
- Matrix Metalloproteinase 1
(metabolism)
- Matrix Metalloproteinase 2
(metabolism)
- Matrix Metalloproteinase 3
(metabolism)
- Matrix Metalloproteinase 9
(metabolism)
- Matrix Metalloproteinases
(metabolism)
- Promegestone
(pharmacology)
- Tissue Inhibitor of Metalloproteinase-1
(metabolism)
- Tissue Inhibitor of Metalloproteinase-2
(metabolism)
- Tissue Inhibitor of Metalloproteinases
(metabolism)
- Tumor Necrosis Factor-alpha
(pharmacology)
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