G protein-coupled estrogen receptor 1 agonist G-1 induces cell cycle arrest in the mitotic phase, leading to apoptosis in endometriosis

Fertil Steril. 2015 May;103(5):1228-35.e1. doi: 10.1016/j.fertnstert.2015.01.026. Epub 2015 Feb 24.

Abstract

Objective: To demonstrate the effects of the selective G protein-coupled estrogen receptor 1 (GPER) agonist G-1 in human ovarian endometriotic stromal cells (ESCs).

Design: Experimental in vitro study.

Setting: University hospital.

Patient(s): A total of 33 patients with ovarian endometrioma.

Intervention(s): Endometriotic stromal cells from ovarian chocolate cysts were treated with the GPER agonist G-1.

Main outcome measure(s): The primary outcomes were cell proliferation, measured using the WST-8 assay; cell cycle, as analyzed using flow cytometry, fluorescent immunocytochemistry, and cytotoxicity; caspase activity, as measured by fluorescent and luminescent enzyme assays; and protein expression levels, as determined by Western blot analysis.

Result(s): G-1 suppressed ESC proliferation in a concentration-dependent manner. The inhibitory effect was not blocked when GPER signaling pathways, including the GPER itself, were inhibited. G-1 induced cell cycle arrest and accumulation in the sub-G1 phase in ESCs. Immunofluorescence analysis demonstrated that G-1 interrupted microtubule assembly at the mitotic phase. G-1 also induced caspase-3-dependent apoptosis without significant cytotoxicity.

Conclusion(s): G-1 suppressed proliferation and induced apoptosis in ESCs, suggesting the potential use of this compound as a therapeutic drug for the treatment of endometriosis.

Keywords: G-1; GPER; apoptosis; cell cycle arrest; endometriosis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Apoptosis / drug effects*
  • Caspase 3 / metabolism
  • Cell Proliferation / drug effects*
  • Cells, Cultured
  • Cyclopentanes / pharmacology*
  • Dose-Response Relationship, Drug
  • Endometriosis / genetics
  • Endometriosis / metabolism*
  • Endometriosis / pathology
  • Female
  • Humans
  • M Phase Cell Cycle Checkpoints / drug effects*
  • Microtubules / drug effects
  • Microtubules / metabolism
  • Middle Aged
  • Ovarian Cysts / genetics
  • Ovarian Cysts / metabolism*
  • Ovarian Cysts / pathology
  • Ovary / drug effects*
  • Ovary / metabolism
  • Ovary / pathology
  • Quinolines / pharmacology*
  • RNA Interference
  • Receptors, Estrogen / genetics
  • Receptors, Estrogen / metabolism
  • Receptors, G-Protein-Coupled / agonists*
  • Receptors, G-Protein-Coupled / genetics
  • Receptors, G-Protein-Coupled / metabolism
  • Signal Transduction / drug effects
  • Stromal Cells / drug effects*
  • Stromal Cells / metabolism
  • Stromal Cells / pathology
  • Transfection

Substances

  • 1-(4-(6-bromobenzo(1,3)dioxol-5-yl)-3a,4,5,9b-tetrahydro-3H-cyclopenta(c)quinolin-8-yl)ethanone
  • Cyclopentanes
  • GPER1 protein, human
  • Quinolines
  • Receptors, Estrogen
  • Receptors, G-Protein-Coupled
  • CASP3 protein, human
  • Caspase 3