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Beta adrenergic receptor activation inhibits oral cancer migration and invasiveness.
Bravo-Calderón, Diego Mauricio; Assao, Agnes; Garcia, Natália Galvão; Coutinho-Camillo, Cláudia Malheiros; Roffé, Martin; Germano, Janaína Naiara; Oliveira, Denise Tostes.
Afiliação
  • Bravo-Calderón DM; Department of Surgery, Stomatology, Pathology and Radiology, Area of Pathology, Bauru School of Dentistry, University of São Paulo, Brazil. Electronic address: diegom.bravoc@ucuenca.edu.ec.
  • Assao A; Department of Surgery, Stomatology, Pathology and Radiology, Area of Pathology, Bauru School of Dentistry, University of São Paulo, Brazil. Electronic address: agnesassao@gmail.com.
  • Garcia NG; Department of Surgery, Stomatology, Pathology and Radiology, Area of Pathology, Bauru School of Dentistry, University of São Paulo, Brazil. Electronic address: natggalvao@hotmail.com.
  • Coutinho-Camillo CM; International Research Center, A.C.Camargo Cancer Center, São Paulo, SP, Brazil. Electronic address: ccamillo@accamargo.org.br.
  • Roffé M; International Research Center, A.C.Camargo Cancer Center, São Paulo, SP, Brazil. Electronic address: mroffe@accamargo.org.br.
  • Germano JN; International Research Center, A.C.Camargo Cancer Center, São Paulo, SP, Brazil. Electronic address: janaina.germano@accamargo.org.br.
  • Oliveira DT; Department of Surgery, Stomatology, Pathology and Radiology, Area of Pathology, Bauru School of Dentistry, University of São Paulo, Brazil. Electronic address: denisetostes@usp.br.
Arch Oral Biol ; 118: 104865, 2020 Oct.
Article em En | MEDLINE | ID: mdl-32801034
ABSTRACT

OBJECTIVE:

The aim of this study was to verify ß2-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 ß2-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 ß2-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 ß2-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 ß2-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.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Bucais / Carcinoma de Células Escamosas / Receptores Adrenérgicos beta / Invasividade Neoplásica Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Bucais / Carcinoma de Células Escamosas / Receptores Adrenérgicos beta / Invasividade Neoplásica Idioma: En Ano de publicação: 2020 Tipo de documento: Article