Peroxisome proliferator-activated receptor-γ ligand reduced tumor necrosis factor-α-induced interleukin-8 production and growth in endometriotic stromal cells
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PPAR-γ ligands decreased TNF-α-induced IL-8 production and growth in endometriotic stromal cells.
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Abstract
ObjectiveTo evaluate the influence of peroxisome proliferator-activated receptor-gamma (PPAR gamma) ligand (pioglitazone) on tumor necrosis factor-alpha (TNF-alpha)-induced interleukin-8 (IL-8) expression in endometriotic stromal cells (ESCs) and on proliferation of ESCs.DesignProspective study.SettingDepartment of Obstetrics and Gynecology, Tottori University Hospital, Yonago, Japan.Patient(s)Twenty-seven patients who underwent laparoscopic surgery.Intervention(s)The ESCs were obtained from the chocolate cyst linings of ovaries.Main outcome measure(s)The expression of PPAR gamma gene and protein was determined by reverse transcriptase-polymerase chain reaction (RT-PCR) and immunocytochemistry. We determined the effect of pioglitazone on the production of TNF-alpha-induced IL-8 protein in culture supernatant of ESCs using ELISA. The effect of pioglitazone on TNF-alpha-induced proliferation of ESCs was evaluated by 5-bromo-2'-deoxyuridine proliferation assay. The activation of nuclear factor (NF)-kappaB in ESCs was evaluated by Western blot analyses and NF-kappaB transcription factor assays.Result(s)Immunocytochemistry and RT-PCR revealed the expression of PPAR gamma gene and protein in ESCs. The PPAR gamma protein was predominantly located in the cell nucleus. Measurement of IL-8 protein by ELISA showed that adding TNF-alpha (100 pg/mL) significantly increased IL-8 protein. Treating ESCs with 0.1-10 microM of pioglitazone significantly reduced the TNF-alpha-induced IL-8 production. The presence of 0.1-10 microM of pioglitazone significantly suppressed growth of ESCs. The TNF-alpha increased the expression of phosphorylation of inhibitor kappaB (I kappaB). Adding pioglitazone (10 microM) did not influence the expression of phosphorylated inhibitor kappaB (I kappaB). The TNF-alpha markedly increased the intranuclear concentration of p65, and adding pioglitazone (10 microM) significantly reduced the concentration of p65.Conclusion(s)The present study demonstrates for the first time that PPAR gamma is expressed in ESCs, and that pioglitazone reduced IL-8 secretion and the proliferation of ESCs. The PPAR gamma ligand may be an attractive therapeutic agent for endometriosis.
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- Identification of potential differentially methylated gene-related biomarkers in endometriosis 2022
- An Update on the Multifaceted Role of NF-kappaB in Endometriosis 2022
- Peroxisome Proliferator-Activated Receptor Alpha (PPAR-α) as a Regulator of the Angiogenic Profile of Endometriotic Lesions 2022
- Role of inflammation in benign gynecologic disorders: from pathogenesis to novel therapies† 2021
- The Pathogenesis of Endometriosis: Molecular and Cell Biology Insights 2019
- From pathogenesis to clinical practice: Emerging medical treatments for endometriosis 2018
- Low-dose SKA Progesterone and Interleukin-10 modulate the inflammatory pathway in endometriotic cell lines 2017
- Kinase signalling pathways in endometriosis: potential targets for non-hormonal therapeutics 2016
- An Update on Pathophysiology and Medical Management of Endometriosis 2016
- Pathogenesis of Endometriosis: Roles of Retinoids and Inflammatory Pathways 2015
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- Physiologic activation of nuclear factor kappa-B in the endometrium during the menstrual cycle is altered in endometriosis patients 2011
- Peroxisome proliferating activating receptor gamma–independent attenuation of interleukin 6 and interleukin 8 secretion from primary endometrial stromal cells by thiazolidinediones 2011
- Pathogenesis: Epigenetics 2011
- Involvement of the nuclear factor-κB pathway in the pathogenesis of endometriosis 2010
- Involvement of the nuclear factor-kB pathway in the pathogenesis of endometriosis 2010
- Constitutive and Tumor Necrosis Factor-Alpha-Stimulated Activation of Nuclear Factor-KappaB in Immortalized Endometriotic Cells and Their Suppression by Trichostatin A 2010
- Thiazolidinediones as Therapy for Endometriosis: A Case Series 2009
- PPAR-γ expression in peritoneal endometriotic lesions correlates with pain experienced by patients 2009
- A Botanical Extract from Channel Flow Inhibits Cell Proliferation, Induces Apoptosis, and Suppresses CCL5 in Human Endometriotic Stromal Cells1 2009
- Endometriosis 2009
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