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beta 2-adrenergic receptor expression and the effects of norepinephrine and propranolol on various head and neck cancer subtypes

Authors
Kwon, Soon YoungChun, Kyung JuKil, Hong KwonJung, NaraeShin, Hyun-AhJang, Jeon YeobChoi, Hyo GeunOh, Kyoung-HoKim, Min-Su
Issue Date
11월-2021
Publisher
SPANDIDOS PUBL LTD
Keywords
adrenergic beta-antagonists; adrenergic receptor; head and neck neoplasms; norepinephrine; stress
Citation
ONCOLOGY LETTERS, v.22, no.5
Indexed
SCIE
SCOPUS
Journal Title
ONCOLOGY LETTERS
Volume
22
Number
5
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/135867
DOI
10.3892/ol.2021.13065
ISSN
1792-1074
Abstract
The present study aimed to investigate expression of beta 2-adrenergic receptor (AR), the effect of the stress-related neurotransmitter norepinephrine (NE) on cell viability, proliferation and the therapeutic effect of propranolol, which is a typical beta-blocker in various type of head and neck cancers for the first time. The beta 2-AR expression was investigated using immunohistochemistry and an immunoreactive scoring (IRS) system in 57 different head and neck cancer specimens, and reverse transcriptase-polymerase chain reaction and western blotting in four head and neck cancer cell lines (HNCCLs). Cell viability and proliferation assays were performed using 0, 1, 5 and 10 mu M of NE and 1 mu M of propranolol in four HNCCLs. The expression of beta 2-AR was positive in the majority of head and neck cancer tissues (55/57, 96.5%); however, it was significantly higher in oral cavity cancer than in pharyngeal cancer (median IRS: 9 vs. 3; P<0.001). All HNCCLs exhibited beta 2-AR expression, with a higher expression level detected in the oral cavity cancer cell line than in the others. NE stimulated viability (oral cavity, 206%; larynx, 156%; pharynx, 130%; nasal cavity, 137%; 10 mu M NE) and proliferation (124, 176, 131 and 127%, respectively) in a dose-dependent manner in all HNCCLs. Conversely, propranolol attenuated such viability (55, 42, 18 and 22%, respectively) and proliferation (22, 40, 61 and 48%, respectively). In conclusion, the viability and proliferation of various head and neck cancers may be directly stimulated by stress and this may be attenuated by beta-blockers.
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