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:
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Authors | Diego Mauricio Bravo-Calderón, Agnes Assao, Natália Galvão Garcia, Cláudia Malheiros Coutinho-Camillo, Martin Roffé, Janaína Naiara Germano, Denise Tostes Oliveira |
Journal | Archives of oral biology
(Arch Oral Biol)
Vol. 118
Pg. 104865
(Oct 2020)
ISSN: 1879-1506 [Electronic] England |
PMID | 32801034
(Publication Type: Journal Article)
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Copyright | Copyright © 2020 Elsevier Ltd. All rights reserved. |
Chemical References |
- Adrenergic beta-Antagonists
- Receptors, Adrenergic, beta
- Propranolol
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Topics |
- Adrenergic beta-Antagonists
(pharmacology)
- Carcinoma, Squamous Cell
(drug therapy, pathology)
- Cell Line, Tumor
- Humans
- Mouth Neoplasms
(drug therapy, pathology)
- Neoplasm Invasiveness
- Propranolol
(pharmacology)
- Receptors, Adrenergic, beta
(metabolism)
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