E2F4-induced AGAP2-AS1 up-regulation accelerates the progression of colorectal cancer via miR-182-5p/CFL1 axis

Dig Liver Dis. 2022 Jul;54(7):878-889. doi: 10.1016/j.dld.2021.08.002. Epub 2021 Nov 24.

Abstract

Background: Long non-coding RNAs (lncRNAs) are closely associated with the pathogenesis of numerous diseases including cancers. LncRNA AGAP2 Antisense RNA 1 (AGAP2-AS1) has been found to participate in the tumorigenesis of several kinds of human cancers. Nonetheless, its potential function in colorectal cancer (CRC) was still poorly investigated.

Methods: The expression level of RNAs or proteins was assessed by RT-qPCR or western blot analysis. Functional experiments were performed to analyze the role of AGAP2-AS1 in CRC in vitro and in vivo. Mechanism investigations were fulfilled to determine the potential mechanism of the molecules.

Results: AGAP2-AS1 expression was significantly elevated in CRC cells and could be transcriptionally activated by E2F Transcription Factor 4 (E2F4). Down-regulated AGAP2-AS1 could weaken CRC cell growth, migration, invasion, and epithelial-mesenchymal transition (EMT). MicroRNA-182-5p (miR-182-5p) was the target downstream molecule of AGAP2-AS1. Furthermore, Cofilin 1 (CFL1) was proved as the target of miR-182-5p. Mechanically, AGAP2-AS1 could boost the CFL1 expression via competitively binding to miR-182-5p in CRC. Importantly, CFL1 restoration could counteract the in vitro and in vivo suppression of depleted AGAP2-AS1 on CRC progression.

Conclusion: E2F4-stimulated AGAP2-AS1 aggravated CRC development through regulating miR-182-5p/CFL1 axis, implying that AGAP2-AS1 might become a potent new target for future therapies for CRC.

Keywords: AGAP2-AS1; CFL1; Colorectal cancer; E2F4; miR-182-5p.

MeSH terms

  • Cell Line, Tumor
  • Cell Movement
  • Cell Proliferation
  • Cofilin 1 / genetics
  • Cofilin 1 / metabolism
  • Colorectal Neoplasms* / genetics
  • Colorectal Neoplasms* / pathology
  • E2F4 Transcription Factor / genetics
  • E2F4 Transcription Factor / metabolism
  • GTP-Binding Proteins / genetics*
  • GTPase-Activating Proteins / genetics*
  • Gene Expression Regulation, Neoplastic
  • Humans
  • MicroRNAs* / genetics
  • MicroRNAs* / metabolism
  • RNA, Long Noncoding* / genetics
  • RNA, Long Noncoding* / metabolism
  • Up-Regulation

Substances

  • CFL1 protein, human
  • Cofilin 1
  • E2F4 Transcription Factor
  • E2F4 protein, human
  • GTPase-Activating Proteins
  • MicroRNAs
  • Mirn182 microRNA, human
  • RNA, Long Noncoding
  • AGAP2 protein, human
  • GTP-Binding Proteins