Heat shock protein 27 expression in areca quid chewing-associated oral squamous cell carcinomas.

doi:10.1111/j.1601-0825.2012.01933.x

中山醫學大學機構典藏 CSMUIR > 口腔醫學院 > 牙醫學系暨碩士班 > 期刊論文 > Item 310902500/11288

Please use this identifier to cite or link to this item: https://ir.csmu.edu.tw:8080/ir/handle/310902500/11288

Title:	Heat shock protein 27 expression in areca quid chewing-associated oral squamous cell carcinomas.
Authors:	Lee, SS Tsai, CH Ho, YC Yu, CC Chang, YC
Contributors:	中山醫學大學
Date:	2012
Issue Date:	2015-07-15T08:05:16Z (UTC)
ISSN:	1354-523X
Abstract:	OBJECTIVES: Heat shock protein (HSP) 27 is a low-molecular-weight protein that functions as a molecular chaperone and plays a cytoprotective role through its antioxidant activity during cell stress. Areca quid chewing is associated with the high incidence of oral squamous cell carcinomas (OSCCs) in Taiwan. The aim of this study was to compare heat shock protein 27 (HSP27) expression in OSCCs and the normal oral tissues. METHODS: Forty-eight OSCCs from areca quid chewers and ten normal oral tissue biopsy samples without areca quid chewing were analyzed by immunohistochemistry for HSP27. The normal human oral keratinocytes (HOKs) were challenged with arecoline, the major alkaloid of areca nut, by Western blot for HSP27. Furthermore, epigallocatechin-3 gallate (EGCG), glutathione precursor N-acetyl-L-cysteine (NAC), cyclooxygenase-2 inhibitor NS-398, HSP inhibitor quercetin, extracellular signal-regulated protein kinase (ERK) inhibitor PD98059, and p38 inhibitor SB203580 were added to find the possible regulatory mechanisms. RESULTS: Heat shock protein 27 exhibited higher expression in OSCCs than normal specimens (P < 0.05). Arecoline was found to elevate HSP27 expression in a dose- and time-dependent manner (P < 0.05). The additions of pharmacological agents were found to inhibit arecoline-induced HSP27 expression (P < 0.05). CONCLUSIONS: Heat shock protein 27 expression is significantly elevated in areca quid chewing-associated OSCCs. Arecoline-induced HSP27 expression was downregulated by EGCG, NS398, NAC, quercetin, PD98059, and SB203580. © 2012 John Wiley & Sons A/S.
URI:	https://ir.csmu.edu.tw:8080/ir/handle/310902500/11288 http://dx.doi.org/10.1111/j.1601-0825.2012.01933.x
Relation:	Oral Dis. 2012 Oct;18(7):713-9.
Appears in Collections:	[牙醫學系暨碩士班] 期刊論文

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