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

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dc.contributor.authorKwon, Soon Young-
dc.contributor.authorChun, Kyung Ju-
dc.contributor.authorKil, Hong Kwon-
dc.contributor.authorJung, Narae-
dc.contributor.authorShin, Hyun-Ah-
dc.contributor.authorJang, Jeon Yeob-
dc.contributor.authorChoi, Hyo Geun-
dc.contributor.authorOh, Kyoung-Ho-
dc.contributor.authorKim, Min-Su-
dc.date.accessioned2022-02-15T13:41:55Z-
dc.date.available2022-02-15T13:41:55Z-
dc.date.created2022-02-08-
dc.date.issued2021-11-
dc.identifier.issn1792-1074-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/135867-
dc.description.abstractThe 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.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherSPANDIDOS PUBL LTD-
dc.subjectBETA-BLOCKERS-
dc.subjectVEGF-C-
dc.subjectRECURRENCE-
dc.titlebeta 2-adrenergic receptor expression and the effects of norepinephrine and propranolol on various head and neck cancer subtypes-
dc.typeArticle-
dc.contributor.affiliatedAuthorOh, Kyoung-Ho-
dc.identifier.doi10.3892/ol.2021.13065-
dc.identifier.scopusid2-s2.0-85115981382-
dc.identifier.wosid000700872300001-
dc.identifier.bibliographicCitationONCOLOGY LETTERS, v.22, no.5-
dc.relation.isPartOfONCOLOGY LETTERS-
dc.citation.titleONCOLOGY LETTERS-
dc.citation.volume22-
dc.citation.number5-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaOncology-
dc.relation.journalWebOfScienceCategoryOncology-
dc.subject.keywordPlusBETA-BLOCKERS-
dc.subject.keywordPlusRECURRENCE-
dc.subject.keywordPlusVEGF-C-
dc.subject.keywordAuthoradrenergic beta-antagonists-
dc.subject.keywordAuthoradrenergic receptor-
dc.subject.keywordAuthorhead and neck neoplasms-
dc.subject.keywordAuthornorepinephrine-
dc.subject.keywordAuthorstress-
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