JARID2 regulates epithelial mesenchymal transition through the PTEN/AKT signalling pathways in ovarian endometriosis

Reprod Biol. 2023 Mar;23(1):100729. doi: 10.1016/j.repbio.2023.100729. Epub 2023 Jan 12.

Abstract

Recently, it has been proposed that epithelial-mesenchymal transition (EMT) plays a key role in the development of endometriosis (EMs). Although EMs is a benign disease, it has the characteristics of malignant tumors, such as invasion and migration. JARID2 (Jumonji, AT rich interaction domain) can induce EMT in cancer cells to increase their invasion and migration abilities. However, whether JARID2 has the same function in EMs is not yet known. In this study, A retrospective immunohistochemistry(IHC) was used to measure the expression of JARID2, E-cadherin, PTEN, and p-AKT in ovarian endometriosis (OE) tissues. JARID2, EMT and PTEN/AKT signaling pathway related indicators were assessed by RT-PCR and western blotting in vitro. Furthermore, functional assays were applied to evaluate the involvement of JARID2 in the invasion and migration of Ishikawa cells. Here,we conclude that JARID2 could be involved in the PTEN/AKT signalling pathway and contribute to the development of ovarian endometriosis. The expression of JARID2 was negatively correlated with PTEN, but positively correlated with p-AKT in the ectopic endometrial tissues of OE cases. JARID2 overexpression increased the expression of N-cadherin, vimentin and AKT, but inhibited the expression of E-cadherin and PTEN. Accordingly, the opposite results were obtainedwhen JARID2 was downregulated. Furthermore, JARID2 promoted the invasion and migration ability of Ishikawa cells.

Keywords: Epithelial-mesenchymal transition; JARID2; Ovarian endometriosis.

MeSH terms

  • Cadherins / metabolism
  • Cell Line, Tumor
  • Cell Movement
  • Cell Proliferation
  • Endometriosis* / metabolism
  • Epithelial-Mesenchymal Transition
  • Female
  • Humans
  • Ovarian Neoplasms* / pathology
  • PTEN Phosphohydrolase / metabolism
  • Polycomb Repressive Complex 2 / metabolism
  • Proto-Oncogene Proteins c-akt / metabolism
  • Retrospective Studies
  • Signal Transduction / physiology

Substances

  • Proto-Oncogene Proteins c-akt
  • Cadherins
  • PTEN protein, human
  • PTEN Phosphohydrolase
  • JARID2 protein, human
  • Polycomb Repressive Complex 2