A 3'-tRNA-derived fragment enhances cell proliferation, migration and invasion in gastric cancer by targeting FBXO47

Arch Biochem Biophys. 2020 Sep 15:690:108467. doi: 10.1016/j.abb.2020.108467. Epub 2020 Jun 24.

Abstract

Increasing evidence demonstrates that tRNA-derived fragments (tRFs) exert important effects and are dysregulated in various human cancer types. However, their roles in gastric cancer (GC) remain unknown. Here we identified the functional effects of tRF-3019a (derived from tRNA-Ala-AGC-1-1) in GC. We demonstrated that tRF-3019a was upregulated in GC tissues and cell lines. Phenotypic studies revealed that tRF-3019a overexpression enhances GC cell proliferation, migration and invasion. Conversely, tRF-3019a knockdown inhibits GC cell malignant activities. Mechanistic investigation implies that tRF-3019a directly regulates tumor suppressor gene FBXO47. Furthermore, tRF-3019a levels may discriminate GC tissues from nontumorous tissues. Taken together, our results reveal that tRF-3019a modulates GC cell proliferation, migration and invasion by targeting FBXO47, and it may serve as a potential diagnostic biomarker for GC.

Keywords: Biomarker; FBXO47; Gastric cancer; tRNA-derived fragment.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Base Sequence
  • Biomarkers, Tumor / metabolism
  • Cell Line, Tumor
  • Cell Movement
  • Cell Proliferation
  • Gene Expression Regulation, Neoplastic
  • Gene Knockdown Techniques
  • Humans
  • Nucleic Acid Conformation
  • RNA, Transfer / metabolism*
  • RNA, Transfer, Amino Acid-Specific / genetics*
  • Stomach Neoplasms / metabolism*
  • Transcription Factors / genetics*
  • Transcription Factors / metabolism*
  • Transfection

Substances

  • Biomarkers, Tumor
  • FBXO47 protein, human
  • RNA, Transfer, Amino Acid-Specific
  • Transcription Factors
  • RNA, Transfer