LncRNA TMPO-AS1 promotes proliferation and migration in bladder cancer

Eur Rev Med Pharmacol Sci. 2020 Sep;24(17):8740-8746. doi: 10.26355/eurrev_202009_22812.

Abstract

Objective: This study aims to uncover the in vitro influences of lncRNA TMPO-AS1 on the progression of bladder cancer (BLCA) and the underlying mechanism.

Patients and methods: Expression levels of TMPO-AS1 in BLCA tissues and normal bladder tissues were analyzed in The Cancer Genome Atlas (TCGA) database. Differential expressions of TMPO-AS1 in BLCA tissues and normal bladder epithelial tissues were detected by quantitative Real Time-Polymerase Chain Reaction (qRT-PCR). Potential influence of TMPO-AS1 on prognosis of BLCA patients was assessed. In vitro influences of TMPO-AS1 on proliferative and migratory abilities in T24 and UMUC-3 cells were evaluated by Cell Counting Kit-8 (CCK-8), transwell, and wound healing assay, respectively. Finally, the correlation between TMPO-AS1 and its sense RNA TMPO was assessed by analyzing TCGA database, clinical samples, and BLCA cell lines.

Results: By analyzing TCGA database and clinical samples, it was found that TMPO-AS1 was upregulated in BLCA tissues compared with that in normal bladder tissues. Worse survival was observed in BLCA patients with high expression of TMPO-AS1. TMPO-AS1 level was correlated to muscle invasiveness and TNM stage of BLCA patients. In T24 and UMUC-3 cells, the knockdown of TMPO-AS1 suppressed proliferative and migratory abilities. TMPO-AS1 level was positively correlated to that of its sense RNA TMPO. Moreover, the knockdown of TMPO-AS1 downregulated mRNA and protein levels of TMPO in BLCA cells.

Conclusions: TMPO-AS1 is upregulated in BLCA tissue and closely linked to poor prognosis of BLCA patients.

MeSH terms

  • Cell Line
  • Cell Movement / genetics
  • Cell Proliferation / genetics
  • Epithelium / metabolism
  • Female
  • Humans
  • Male
  • Middle Aged
  • Nuclear Proteins / genetics*
  • Nuclear Proteins / metabolism
  • Prognosis
  • RNA, Long Noncoding*
  • Thymopoietins / genetics*
  • Thymopoietins / metabolism
  • Urinary Bladder / metabolism
  • Urinary Bladder Neoplasms / genetics*
  • Urinary Bladder Neoplasms / metabolism
  • Urinary Bladder Neoplasms / pathology

Substances

  • Nuclear Proteins
  • RNA, Long Noncoding
  • Thymopoietins
  • TMPO protein, human