Long Noncoding RNA LINC01207 Promotes Colon Cancer Cell Proliferation and Invasion by Regulating miR-3125/TRIM22 Axis

Biomed Res Int. 2020 Nov 22:2020:1216325. doi: 10.1155/2020/1216325. eCollection 2020.

Abstract

Increasing study has validated that long noncoding RNAs (lncRNAs) are involved in the growth and metastasis of colon cancer. LINC01207 has been reported to play vital roles in certain types of cancer, while the precise function of LINC01207 in the progression of colon cancer remains unclear. The objective of this study was to investigate the effect of LINC01207 on the growth and metastasis of colon cancer cells and to explore the underlying mechanism. We found that the expression of LINC01207 was significantly upregulated in colon adenocarcinoma tissues compared with normal tissues by the GEPIA database. Notably, silencing of LINC01207 significantly suppressed the proliferation, migration, and invasion abilities of SW480 and HT-29 cells. Mechanistically, our data demonstrated that LINC01207 could sponge miR-3125 in colon cancer cells. Moreover, miR-3125 could directly target TRIM22 and negatively regulate its expression. Rescue assays revealed that miR-3125 inhibitor or TRIM22 overexpression significantly reversed the repressive role of LINC01207 knockdown in colon cancer cell proliferation and invasion. In conclusion, LINC01207 exerts an oncogenic role in the progression of colon cancer by absorbing miR-3125 to modulating TRIM22 expression.

MeSH terms

  • Apoptosis / genetics
  • Carcinogenesis / genetics
  • Cell Line, Tumor
  • Cell Movement
  • Cell Proliferation
  • Colonic Neoplasms / genetics*
  • Colonic Neoplasms / metabolism
  • Disease Progression
  • Gene Expression Regulation, Neoplastic
  • Gene Silencing*
  • HT29 Cells
  • Humans
  • MicroRNAs / metabolism*
  • Minor Histocompatibility Antigens / genetics*
  • Minor Histocompatibility Antigens / metabolism
  • Neoplasm Invasiveness
  • RNA, Long Noncoding*
  • Repressor Proteins / genetics*
  • Repressor Proteins / metabolism
  • Tripartite Motif Proteins / genetics*
  • Tripartite Motif Proteins / metabolism
  • Up-Regulation

Substances

  • MIRN3125 microRNA, human
  • MicroRNAs
  • Minor Histocompatibility Antigens
  • RNA, Long Noncoding
  • Repressor Proteins
  • TRIM22 protein, human
  • Tripartite Motif Proteins