Beta adrenergic receptor activation inhibits oral cancer migration and invasiveness

Arch Oral Biol. 2020 Oct:118:104865. doi: 10.1016/j.archoralbio.2020.104865. Epub 2020 Aug 7.

Abstract

Objective: The aim of this study was to verify β2-AR expression in oral squamous cell carcinoma cell lines (SCC-9 and SCC-25), and to investigate the role of this receptor in migration and invasion of these neoplastic cells.

Design: SCC-9 and SCC-25 cells were investigated for gene and protein expression of β2-AR. Cell migration and invasion were analyzed by wound healing assay and transwell invasion camera system. Different concentrations (0.1, 1 and 10 μM) of norepinephrine were used to stimulate, and 1 μM propranolol was used to block the beta-adrenergic receptors on cancer cells. Differences in median values of SCC-9 and SCC-25 and β2-AR protein expression were analyzed by Friedman test and in case of significant differences; pairwise comparisons were performed using Bonferroni correction.

Results: The results showed that the β2-AR gene and protein expression were observed in both oral cancer cell lines. The concentration of 10 μM of norepinephrine significantly inhibited (p ≤ 0.05) migration of SCC-9 and SCC-25 cell lines. Furthermore, there was a significant reduction (p ≤ 0.05) in the effect of norepinephrine on cell migration when the β2-AR was inhibited by propranolol. The blockade by propranolol showed a tendency to reverse the effect of norepinephrine on the invasiveness of SCC-9 and SCC-25.

Conclusions: The use of beta-adrenergic receptor agonists could become an adjuvant therapeutic target in the treatment of this malignancy.

Keywords: Oral cancer; beta(2)-adrenergic receptor; stress.

MeSH terms

  • Adrenergic beta-Antagonists / pharmacology
  • Carcinoma, Squamous Cell / drug therapy
  • Carcinoma, Squamous Cell / pathology*
  • Cell Line, Tumor
  • Humans
  • Mouth Neoplasms / drug therapy
  • Mouth Neoplasms / pathology*
  • Neoplasm Invasiveness*
  • Propranolol / pharmacology
  • Receptors, Adrenergic, beta / metabolism*

Substances

  • Adrenergic beta-Antagonists
  • Receptors, Adrenergic, beta
  • Propranolol