Effects of multiple-target anti-microRNA antisense oligodeoxyribonucleotides on proliferation and migration of gastric cancer cells

Asian Pac J Cancer Prev. 2012;13(7):3203-7. doi: 10.7314/apjcp.2012.13.7.3203.

Abstract

Backgrounds: To investigate the inhibiting effects of multi-target anti-microRNA antisense oligonucleotide (MTg-AMOs) on proliferation and migration of human gastric cancer cells.

Methods: Single anti-microRNA antisense oligonucleotides (AMOs) and MTg-AMOs for miR-221, 21, and 106a were designed and transfected into SGC7901, a gastric cancer cell line, to target the activity of these miRNAs. Their expression was analyzed using stem-loop RT-PCR and effects of MTg-AMOs on human gastric cancer cells were determined using the following two assay methods: CCK8 for cell proliferation and transwells for migration.

Results: In the CCK-8 cell proliferation assay, 0.6 μmol/L was selected as the preferred concentration of MTg-AMOs and incubation time was 72 hours. Under these experimental conditions, MTg-AMOs demonstrated better suppression of the expression of miR-221, miR-106a, miR-21 in gastric cancer cells than that of single AMOs (P = 0.014, 0.024; 0.038, respectively). Migration activity was also clearly decreased as compared to those in randomized and blank control groups (28 ± 4 Vs 54 ± 3, P <0.01; 28 ± 4 Vs 59 ± 4, P < 0.01).

Conclusions: MTg-AMOs can specifically inhibit the expression of multiple miRNAs, and effectively antagonize proliferation and migration of gastric cancer cells promoted by oncomirs.

Publication types

  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Growth Processes / drug effects
  • Cell Growth Processes / genetics
  • Cell Line, Tumor
  • Cell Movement / drug effects*
  • Cell Movement / genetics
  • Gene Expression Regulation, Neoplastic / drug effects
  • Humans
  • MicroRNAs / antagonists & inhibitors*
  • MicroRNAs / genetics*
  • Oligodeoxyribonucleotides, Antisense / genetics*
  • Oligodeoxyribonucleotides, Antisense / pharmacology*
  • Sincalide / genetics
  • Stomach Neoplasms / genetics*
  • Stomach Neoplasms / therapy*
  • Transfection / methods

Substances

  • MicroRNAs
  • Oligodeoxyribonucleotides, Antisense
  • Sincalide