Circular RNA ARHGAP26 is over-expressed and its downregulation inhibits cell proliferation and promotes cell apoptosis in gastric cancer cells

Saudi J Gastroenterol. 2019 Mar-Apr;25(2):119-125. doi: 10.4103/sjg.SJG_283_18.

Abstract

Background/aims: This study aimed to explore the effect of circular RNA ARHGAP26 (circ-ARHGAP26) on cell proliferation and apoptosis in gastric cancer (GC) cell lines.

Materials and methods: Human GC cell lines including HGC-27, AGS, SGC-7901, BGC-823, NCI-N87 and human normal gastric mucosal cells GSE-1 were cultured. The circ-ARHGAP26 expression was determined by quantitative polymerase chain reaction assay. Blank inhibitor and circ-ARHGAP26 inhibitor plasmids were transfected into HGC-27 or AGS cells as NC (-) and circ-ARHGAP26(-) groups. Counting Kit-8 (CCK-8) and Annexin V (AV)/propidium iodide (PI) were conducted to evaluate cell proliferation and cell apoptosis, respectively. Western blot was performed to determine the expressions of apoptotic markers (C-Caspase3 and Bcl-2).

Results: The circ-ARHGAP26 expression was elevated in HGC-27 (P < 0.001), AGS (P < 0.001), SGC-7901 (P < 0.01), BGC-823 (P < 0.05) and NCI-N87 (P < 0.05) GC cell lines compared to GSE-1 cells. In HGC-27 cells, CCK8 assay revealed that cell proliferation was decreased at 48 h (P < 0.05) and 72 h (P < 0.01), while AV/PI assay disclosed that cell apoptosis rate was increased at 72 h in circ-ARHGAP26 (-) group compared to NC (-) group (P < 0.01). Western blot assay also illuminated that apoptotic marker C-Caspase 3 was raised, while anti-apoptotic marker Bcl-2 was reduced at 72 h in circ-ARHGAP26 (-) group compared to NC (-) group. In addition, further validation in AGS cells also exhibited that cells proliferation was repressed, while apoptosis was enhanced in circ-ARHGAP26 (-) group compared to NC (-) group.

Conclusion: The circ-ARHGAP26 is over-expressed and its downregulation inhibits cell proliferation and promotes cells apoptosis in GC cells.

Keywords: ARHGAP26; Apoptosis; circular RNA; gastric cancer; proliferation.

Publication types

  • Comparative Study

MeSH terms

  • Apoptosis / genetics*
  • Cell Line, Tumor / metabolism
  • Cell Proliferation / genetics*
  • Down-Regulation
  • GTPase-Activating Proteins / metabolism
  • Gastric Mucosa / metabolism
  • Gene Expression Regulation, Neoplastic / genetics
  • Humans
  • RNA / genetics*
  • RNA, Circular
  • Stomach Neoplasms / genetics*
  • Stomach Neoplasms / pathology

Substances

  • ARHGAP26 protein, human
  • GTPase-Activating Proteins
  • RNA, Circular
  • RNA