LncRNA BCRT1 facilitates osteosarcoma progression via regulating miR-1303/FGF7 axis

Aging (Albany NY). 2021 Jun 8;13(11):15501-15510. doi: 10.18632/aging.203106. Epub 2021 Jun 8.

Abstract

Growing studies noted that lncRNA was closely related with the initiation and progression of tumors. However, the role of BCRT1 in the progression of osteosarcoma remains unknown. We noted that BCRT1 is significantly upregulated in osteosarcoma specimens and cells. Elevated expression of BCRT1 promotes cell growth and cell cycle in osteosarcoma cell. Moreover, BCRT1 induces EMT and secretion of inflammatory mediators in osteosarcoma cell. We illustrated that elevated expression of BCRT1 decreases miR-1303 expression in MG-63 cell. The expression of miR-1303 is lower in osteosarcoma specimens than in non-tumor specimens. There is an inverse interrelation between miR-1303 levels and BCRT1 levels in osteosarcoma specimens. Furthermore, we identified FGF7 is one direct target gene of miR-1303 in osteosarcoma cell. Ectopic expression of miR-1303 suppresses FGF7 expression and elevated expression of BCRT1 enhanced FGF7 expression in MG-63 cell. Finally, we illustrated that BCRT1 induces osteosarcoma cell cycle and proliferation and promotes EMT progression and inflammatory mediators secretion via modulating FGF7 expression. Our study suggested that BCRT1 acts as one oncogene in osteosarcoma progression.

Keywords: BCRT1; FGF7; miR-1303; osteosarcoma.

MeSH terms

  • Base Sequence
  • Bone Neoplasms / genetics*
  • Bone Neoplasms / pathology
  • Cell Cycle / genetics
  • Cell Line, Tumor
  • Cell Proliferation / genetics
  • Disease Progression*
  • Down-Regulation / genetics
  • Epithelial-Mesenchymal Transition / genetics
  • Fibroblast Growth Factor 7 / genetics*
  • Fibroblast Growth Factor 7 / metabolism
  • Gene Expression Regulation, Neoplastic*
  • Humans
  • Inflammation Mediators / metabolism
  • MicroRNAs / genetics*
  • MicroRNAs / metabolism
  • Osteosarcoma / genetics*
  • Osteosarcoma / pathology*
  • RNA, Long Noncoding / genetics
  • RNA, Long Noncoding / metabolism*
  • Signal Transduction / genetics
  • Up-Regulation / genetics

Substances

  • Inflammation Mediators
  • MIRN1303 microRNA, human
  • MicroRNAs
  • RNA, Long Noncoding
  • Fibroblast Growth Factor 7