CircTHBS1 targeting miR-211/CCND2 pathway to promote cell proliferation and migration potential in primary cystitis glandularis cells

Biosci Rep. 2021 Aug 27;41(8):BSR20201164. doi: 10.1042/BSR20201164.

Abstract

The pathogenesis of cystitis glandular (CG) is unclear, but it is generally considered to be a neoplastic lesion of urothelial hyperplasia formed by long-term chronic stimulation. There is growing evidence that circRNAs play important roles in a variety of cellular processes. However, there are few reports on the role and molecular mechanism of circRNA in CG. In the present study, we first isolated primary cells from CG tissues and adjacent normal tissues. Further experiments showed that CircTHBS1 was up-regulated in primary CG cells (pCGs). The results of CCK-8 showed that the overexpression of CircTHBS1 promoted the viability of pCGs, while the deletion of CircTHBS1 reduced the cell viability. Knocking out CircTHBS1 also inhibited the migration of pCGs. In addition, we demonstrated that CircTHBS1 played a role in the adsorption of miR-211 by "sponge" in pCG. In turn, miR-211 can directly target CYCLIN D2 (CCND2) 3'UTR to perform its function. Finally, we confirmed the role and mechanism of CircTHBS1/miR-211/CCND2 regulation axis in pCGs. In summary, our study is the first to reveal the role and underlying mechanism of CircTHBS1 in CG, providing a potential biomarker and therapeutic target for human CG.

Keywords: CCND2; CircTHBS1; Cystitis glandularis; ceRNA; miR-211.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Case-Control Studies
  • Cell Movement*
  • Cell Proliferation*
  • Cells, Cultured
  • Cyclin D2 / genetics
  • Cyclin D2 / metabolism*
  • Cystitis / genetics
  • Cystitis / metabolism*
  • Cystitis / pathology
  • Gene Expression Regulation
  • Humans
  • MicroRNAs / genetics
  • MicroRNAs / metabolism*
  • Mucous Membrane / metabolism*
  • Mucous Membrane / pathology
  • RNA, Circular / genetics
  • RNA, Circular / metabolism*
  • Signal Transduction
  • Urinary Bladder / metabolism*
  • Urinary Bladder / pathology

Substances

  • CCND2 protein, human
  • Cyclin D2
  • MIRN211 microRNA, human
  • MicroRNAs
  • RNA, Circular