LncRNA MNX1-AS1 sustains inactivation of Hippo pathway through a positive feedback loop with USP16/IGF2BP3 axis in gallbladder cancer

Cancer Lett. 2022 Oct 28:547:215862. doi: 10.1016/j.canlet.2022.215862. Epub 2022 Aug 8.

Abstract

The long non-coding RNAs (lncRNAs) have been implicated in multiple human cancers, which may offer great potential as putative targets for cancer diagnosis and treatment. However, the roles of most lncRNAs in gallbladder cancer (GBC) remain poorly understood. The objective of this research involves investigating the clinical implications and underlying mechanism of lncRNA motor neuron and pancreas homeobo×1 antisense RNA 1 (MNX1-AS1) in GBC. This study shows that MNX1-AS1 expression is elevated in the tissues of GBC patients, and is strongly associated with reduced patient survival. Functionally, MNX1-AS1 significantly stimulates the proliferation and metastasis of GBC cells in vitro and in vivo. Mechanistically, MNX1-AS1 is transcriptionally activated by TEA domain family member 4 (TEAD4), and suppresses insulin-like growing factor 2 mRNA-binding protein 3 (IGF2BP3) degradation by recruiting ubiquitin specific peptidase 16 (USP16). Furthermore, MNX1-AS1/IGF2BP3 axis inhibits the Hippo signaling pathway and subsequently activates TEAD4, thereby forming a positive feedback loop. According to our results, MNX1-AS1 facilitates tumorigenesis, progression and metastasis of GBC through a MNX1-AS1/IGF2BP3/Hippo pathway positive feedback loop, which could be both diagnostically and therapeutically helpful in GBC.

Keywords: Cancer progression; Deubiquitinase; GBC; Scaffold; TEAD4.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Line, Tumor
  • Cell Movement / genetics
  • Cell Proliferation / genetics
  • Feedback
  • Gallbladder Neoplasms* / genetics
  • Gene Expression Regulation, Neoplastic
  • Hippo Signaling Pathway
  • Homeodomain Proteins / genetics
  • Humans
  • Insulin / metabolism
  • MicroRNAs* / genetics
  • RNA, Long Noncoding* / genetics
  • RNA, Messenger
  • RNA-Binding Proteins / genetics
  • TEA Domain Transcription Factors
  • Transcription Factors / genetics
  • Transcription Factors / metabolism
  • Ubiquitin Thiolesterase

Substances

  • Homeodomain Proteins
  • IGF2BP3 protein, human
  • Insulin
  • MNX1 protein, human
  • MicroRNAs
  • RNA, Long Noncoding
  • RNA, Messenger
  • RNA-Binding Proteins
  • TEA Domain Transcription Factors
  • TEAD4 protein, human
  • Transcription Factors
  • USP16 protein, human
  • Ubiquitin Thiolesterase