Reduced MAGI3 level by HPV18E6 contributes to Wnt/β-catenin signaling activation and cervical cancer progression

FEBS Open Bio. 2021 Nov;11(11):3051-3062. doi: 10.1002/2211-5463.13298. Epub 2021 Oct 1.

Abstract

Human papillomavirus type 18 (HPV18) has high carcinogenic power in invasive cervical cancer (ICC) development. However, the underlying mechanism remains elusive. The carcinogenic properties of HPV18 require the PDZ-binding motif of its E6 oncoprotein (HPV18 E6) to degrade its target PSD95/Dlg/ZO-1 (PDZ) proteins. In this study, we demonstrated that the PDZ protein membrane-associated guanylate kinase, WW and PDZ domain containing 3 (MAGI3) inhibited the Wnt/β-catenin pathway, and subsequently cervical cancer (CC) cell migration and invasion, via decreasing β-catenin levels. By reducing MAGI3 protein levels, HPV18 E6 promoted CC cell migration and invasion through activation of Wnt/β-catenin signaling. Furthermore, HPV18 rather than HPV16 was preferentially associated with the downregulation of MAGI3 and activation of the Wnt/β-catenin pathway in CC. These findings shed light on the mechanism that gives HPV18 its high carcinogenic potential in CC progression.

Keywords: HPV; MAGI3; PDZ; Wnt/β-catenin; cervical cancer; invasion.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptor Proteins, Signal Transducing / metabolism
  • Cell Line, Tumor
  • Cell Movement / genetics
  • China
  • Female
  • Gene Expression Regulation, Neoplastic
  • Human papillomavirus 18 / metabolism
  • Human papillomavirus 18 / pathogenicity
  • Humans
  • Membrane Proteins / genetics
  • Membrane Proteins / metabolism*
  • Neoplasm Invasiveness / genetics
  • Oncogene Proteins, Viral / metabolism
  • Papillomavirus Infections
  • Repressor Proteins / metabolism
  • Transcription Factors / metabolism
  • Uterine Cervical Neoplasms / metabolism*
  • Uterine Cervical Neoplasms / physiopathology
  • Wnt Signaling Pathway / genetics
  • Wnt Signaling Pathway / physiology*
  • beta Catenin / metabolism

Substances

  • Adaptor Proteins, Signal Transducing
  • MAGI3 protein, human
  • Membrane Proteins
  • Oncogene Proteins, Viral
  • Repressor Proteins
  • Transcription Factors
  • beta Catenin