Heparin is a promising agent for the treatment of endometriosis-associated fibrosis
Lab / animal
OA: bronze
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⤵ 13 in-corpus citations
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This study investigated heparin as a potential treatment for endometriosis-associated fibrosis, finding it to be a promising agent.
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Abstract
OBJECTIVE: To assess the use of heparin for the medical treatment of endometriosis-associated fibrosis.
DESIGN: The effects of heparin on the endometriotic stromal cells (ECSCs)-mediated contractility were investigated.
SETTING: Research laboratory at a medical school.
PATIENT(S): Endometriotic tissues from nine patients were used.
INTERVENTION(S): Endometriotic stromal cells were cultured three dimensionally in the presence of heparin.
MAIN OUTCOME MEASURE(S): The contractility of ECSCs was assessed by collagen gel contraction assay. Heparin-induced morphological changes of ECSCs were evaluated by laser scanning microscopy. The expression of contractility-related molecules in ECSCs was examined by Western blot analysis.
RESULT(S): In the presence of 10% fetal bovine serum, treated ECSCs showed significant collagen gel contractility (75.9% decrease in surface area after 48 hour vs. 0 hour controls). Endometriotic stromal cell-mediated gel contraction was significantly attenuated in the presence of heparin in a dose-dependent manner (55.7% reduction of the gel contraction at a concentration of 100 microg/mL of heparin sodium versus untreated controls after 48 hours). Heparin suppressed the ECSC attachment to collagen fibers. The expression of alpha-smooth muscle actin, Ras homology (Rho) A, Rho-associated coiled-coil-forming protein kinase (ROCK)-I, and ROCK-II was down-regulated by heparin administration.
CONCLUSION(S): The present study suggests that heparin is a promising agent for the treatment of endometriosis-associated fibrosis. The inhibition of myofibroblastic differentiation, the attenuation of attachment to collagen fibers, and the suppression of Rho-ROCK-mediated pathway activation in ECSCs are involved in the action mechanisms of heparin.
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References (36)
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Cited by (14)
- Endometriosis-associated Pain: Mechanism, Neuroimmune Signature, and Translational Precision Strategies 2026
- The role of fibrosis in endometriosis: a systematic review 2024
- Endometriosis, the Silent Disease: Molecular Targets, Active Principles, and Drug Delivery Systems 2022
- New Therapeutics in Endometriosis: A Review of Hormonal, Non-Hormonal, and Non-Coding RNA Treatments 2021
- Pharmaceuticals targeting signaling pathways of endometriosis as potential new medical treatment: A review 2021
- Chemokine expression profiles of ovarian endometriotic stromal cells in three-dimensional culture 2020
- Revealing the enigma of coagulation in endometriosis: the risk of thrombosis and the role of antithrombotic treatment 2020
- Biological characteristics of endometriotic mesenchymal stem cells isolated from ectopic lesions of patients with endometriosis 2020
- β-catenin signaling inhibitors ICG-001 and C-82 improve fibrosis in preclinical models of endometriosis 2019
- Platelets drive smooth muscle metaplasia and fibrogenesis in endometriosis through epithelial-mesenchymal transition and fibroblast-to-myofibroblast transdifferentiation 2016
- Dysregulated cell mechanical properties of endometrial stromal cells from endometriosis patients 2014
- Potential New Drugs for Endometriosis: Experimental Evidence 2014
- Fasudil inhibits the proliferation and contractility and induces cell cycle arrest and apoptosis of human endometriotic stromal cells: a promising agent for the treatment of endometriosis 2011
- Mevalonate-Ras Homology (Rho)/Rho-Associated Coiled-Coil-Forming Protein Kinase (ROCK)-Mediated Signaling Pathway as a Therapeutic Target for the Treatment of Endometriosis-Associated Fibrosis 2010
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- europepmc
- last seen: 2026-10-14T06:08:39.101224+00:00
- openalex
- last seen: 2026-06-10T17:14:06.276822+00:00
- pubmed
- last seen: 2026-10-08T21:06:23.467768+00:00
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