SNHG22 promotes migration and invasion of trophoblasts via miR-128-3p/PCDH11X axis and activates PI3K/Akt signaling pathway

Clinics (Sao Paulo). 2022 Jun 6:77:100055. doi: 10.1016/j.clinsp.2022.100055. eCollection 2022.

Abstract

Objectives: Long non-coding RNAs (LncRNAs) act as an indispensable role in the Preeclampsia (PE)-related trophoblast function, while its relationship with Small Nucleolar RNA Host Gene 22 (SNHG22) remains unknown. Hence, this study aimed to investigate the roles of lncRNA SNHG22 in the Preeclampsia (PE)-related trophoblasts function and the underlying mechanism.

Method: Normal placentas and placentas from PE patients were collected to detect the expression of lncRNA SNHG22. Then, trophoblasts HTR-8/Svneo and JEG-3 were purchased, cultured, and treated to investigate the roles of lncRNA SNHG22 on cell migration and invasion as well as its underlying regulatory mechanism.

Results: The SNHG22 was downregulated in PE patients, and it was found that SNHG22 overexpression could drive migration and invasion of trophoblasts, while SNHG22 depletion exerted a suppressive effect. Mechanistically, SNHG22 was validated to regulate microRNA-128-3p (miR-128-3p), and Protocadherin 11 X-Linked (PCDH11X) was identified as the target gene of miR-128-3p. Furthermore, it was found that SNHG22 acted as a promoter in the migration and invasion of trophoblast cells in a miR-128-3p/PCDH11X dependent manner, and SNHG22 silencing weakened the activation of PCDH11X-mediated PI3K/Akt signaling pathways through inhibiting miR-128-3p, thereby preventing migration and invasion of trophoblasts.

Conclusion: SNHG22 acted as a driver in the migration and invasion of trophoblasts and may be considered a candidate for the amelioration of PE.

Keywords: Migration; PCDH11X; Preeclampsia; SNHG22; Trophoblast; miR-128-3p.

MeSH terms

  • Cell Line, Tumor
  • Cell Movement / genetics
  • Cell Proliferation
  • Female
  • Humans
  • MicroRNAs* / genetics
  • Phosphatidylinositol 3-Kinases / metabolism
  • Placenta
  • Pre-Eclampsia* / genetics
  • Pregnancy
  • Proto-Oncogene Proteins c-akt / metabolism
  • Protocadherins / metabolism
  • RNA, Long Noncoding / genetics*
  • RNA, Long Noncoding / metabolism
  • Signal Transduction / physiology
  • Trophoblasts

Substances

  • MIRN128 microRNA, human
  • MicroRNAs
  • PCDH11X protein, human
  • Protocadherins
  • RNA, Long Noncoding
  • SNHG32 lncRNA, human
  • Proto-Oncogene Proteins c-akt