MICAL2 contributes to gastric cancer cell migration via Cdc42-dependent activation of E-cadherin/β-catenin signaling pathway

Cell Commun Signal. 2022 Sep 5;20(1):136. doi: 10.1186/s12964-022-00952-x.

Abstract

Background: Gastric cancer is a common and lethal human malignancy worldwide and cancer cell metastasis is the leading cause of cancer-related mortality. MICAL2, a flavoprotein monooxygenase, is an important regulator of epithelial-to-mesenchymal transition. The aim of this study was to explore the effects of MICAL2 on gastric cancer cell migration and determine the underlying molecular mechanisms.

Methods: Cell migration was examined by wound healing and transwell assays. Changes in E-cadherin/β-catenin signaling were determined by qPCR and analysis of cytoplasmic and nuclear protein fractions. E-cadherin/β-catenin binding was determined by co-immunoprecipitation assays. Cdc42 activity was examined by pulldown assay.

Results: MICAL2 was highly expressed in gastric cancer tissues. The knockdown of MICAL2 significantly attenuated migratory ability and β-catenin nuclear translocation in gastric cancer cells while LiCl treatment, an inhibitor of GSK3β, reversed these MICAL2 knockdown-induced effects. Meanwhile, E-cadherin expression was markedly enhanced in MICAL2-depleted cells. MICAL2 knockdown led to a significant attenuation of E-cadherin ubiquitination and degradation in a Cdc42-dependent manner, then enhanced E-cadherin/β-catenin binding, and reduced β-catenin nuclear translocation.

Conclusions: Together, our results indicated that MICAL2 promotes E-cadherin ubiquitination and degradation, leading to enhanced β-catenin signaling via the disruption of the E-cadherin/β-catenin complex and, consequently, the promotion of gastric cell migration. Video Abstract.

Keywords: E-cadherin/β-catenin complex; Gastric cancer; MICAL2; Migration.

Publication types

  • Video-Audio Media
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antigens, CD* / genetics
  • Antigens, CD* / metabolism
  • Cadherins* / genetics
  • Cadherins* / metabolism
  • Cell Line, Tumor
  • Cell Movement / genetics
  • Cell Movement / physiology
  • Cell Proliferation
  • Epithelial-Mesenchymal Transition
  • Humans
  • Microfilament Proteins* / genetics
  • Microfilament Proteins* / metabolism
  • Oxidoreductases* / genetics
  • Oxidoreductases* / metabolism
  • Signal Transduction
  • Stomach Neoplasms* / genetics
  • Stomach Neoplasms* / metabolism
  • Stomach Neoplasms* / pathology
  • Wnt Signaling Pathway
  • beta Catenin* / genetics
  • beta Catenin* / metabolism
  • cdc42 GTP-Binding Protein* / genetics
  • cdc42 GTP-Binding Protein* / metabolism

Substances

  • Antigens, CD
  • CDH1 protein, human
  • Cadherins
  • Microfilament Proteins
  • beta Catenin
  • MICAL2 protein, human
  • Oxidoreductases
  • CDC42 protein, human
  • cdc42 GTP-Binding Protein