JeHoon Lee, M.S.a, Sakhila K. Banu, Ph.D.a, Royce Rodriguez, B.S.a, Anna Starzinski-Powitz, Ph.D.b, Joe A. Arosh, Ph.D.a
a Reproductive Endocrinology and Cell Signaling Laboratory, Department of Integrative Biosciences, College of Veterinary Medicine and Biomedical Sciences, Texas A&M University, College Station, Texas
b Molekulare Zellbiologie und Humangenetik, Institut fur Zellbiologie und Neurowissenschaft, Johann Wolfgang Goethe-Universitat, Frankfurt am Main, Germany
Reprint requests: Joe A. Arosh., Ph.D., Department of Integrative Biosciences, College of Veterinary Medicine & Biomedical Sciences, Mail Stop: TAMU 4458, Texas A&M University, College Station, TX 77843
Objective
To determine interactions between prostaglandin (PG) E2 signaling and proliferation of endometriotic cells to increase our knowledge about PGE2 signaling in the pathogenesis of endometriosis in humans.
Design
Immortalized human endometriotic epithelial and stromal cells were used as an in vitro model. Effects of inhibition of PGE2 receptors on proliferation of endometriotic cells and associated cell cycle regulation were determined.
Setting
College Veterinary Medicine and Biomedical Sciences, Texas A&M University.
Patient(s)
Not available.
Intervention(s)
None.
Main Outcome Measure(s)
Cell proliferation, cell viability, cell cycle, regulation of cyclins, cyclin-dependent kinases, and cyclin-dependent kinase inhibitors.
Result(s)
Selective blockade of EP2/EP4 inhibited proliferation of human endometriotic cells by inducing cell cycle arrest at the G1-S and G2-M checkpoints in epithelial cells and at the G2-M checkpoint in stromal cells. This cell cycle arrest during specific checkpoints was associated with distinct regulation of respective cyclins and cyclin-dependent kinases. Inhibition of EP1 did not decrease endometriotic cell proliferation.
Conclusion(s)
For the first time data from the present study provide a direct molecular link between PGE2 signaling and proliferation of endometriotic cells and suggest that inhibition of EP2/EP4 could be a potential nonestrogen (E) treatment option for endometriosis in women.
Key Words : PGE2 signaling; EP receptors; cell proliferation; cell cycle; immortalized endometriotic cells; endometriosis; humans