Areca nut-induced buccal mucosa fibroblast contraction and its signaling: A potential role in oral submucous fibrosis-a precancer condition

Mei Chi Chang, Li Deh Lin, Hui Lin Wu, Yuan Soon Ho, Hsiang Chi Hsien, Tong Mei Wang, Po Yuan Jeng, Ru Hsiu Cheng, Liang Jiunn Hahn, Jiiang Huei Jeng

研究成果: 雜誌貢獻文章

24 引文 (Scopus)

摘要

Betel quid (BQ) chewing is an oral habit that increases the risk of oral cancer and oral submucous fibrosis (OSF), a precancerous condition showing epithelial atrophy and tissue fibrosis. Persistent fibroblast contraction may induce the fibrotic contracture of tissue. In this study, we found that areca nut extract (ANE) (200-1200 μg/ ml) stimulated buccal mucosa fibroblast (OMF)-populated collagen gel contraction. Arecoline but not arecaidine-two areca alkaloids, slightly induced the OMF contraction. Exogenous addition of carboxylesterase (2 U/ml) prevented the arecoline- but not ANEinduced OMF contraction. OMF expressed inositol triphosphate (IP3) receptors. ANE-induced OMF (800 μg/ml) contraction was inhibited by U73122 [phospholipase C (PLC) inhibitor] and 2-aminoethoxydiphenyl borate (IP3 receptor antagonist), respectively. Ethylene glycol tetraacetic acid and verapamil, two calcium mobilization modulators, also suppressed the ANE-induced OMF contraction. ANE induced calcium/calmodulin kinase II and myosin light chain (MLC) phosphorylation in OMF. Moreover, W7 (a Ca2+/ calmodulin inhibitor), HA1077 (Rho kinase inhibitor), ML-7 (MLC kinase inhibitor) and cytochalasin B (actin filament polymerization inhibitor) inhibited the ANE-induced OMF contraction. Although ANE elevated reactive oxygen species (ROS) level in OMF, catalase, superoxide dismutase and N-acetyl-l-cysteine showed no obvious effect on ANE-elicited OMF contraction. These results indicate that BQ chewing may affect the wound healing and fibrotic processes in OSF via inducing OMF contraction by ANE and areca alkaloids. AN components-induced OMF contraction was related to PLC/ IP3/Ca2+/calmodulin and Rho signaling pathway as well as actin filament polymerization, but not solely due to ROS production.

原文英語
頁(從 - 到)1096-1104
頁數9
期刊Carcinogenesis
34
發行號5
DOIs
出版狀態已發佈 - 五月 2013

指紋

Oral Submucous Fibrosis
Areca
Nuts
Mouth Mucosa
Fibroblasts
Inositol 1,4,5-Trisphosphate Receptors
Arecoline
Mouth Neoplasms
Mastication
Type C Phospholipases
Calmodulin
Actin Cytoskeleton
Alkaloids
Polymerization
Reactive Oxygen Species
Precancerous Conditions
Calcium
Myosin-Light-Chain Kinase
rho-Associated Kinases
Carboxylesterase

ASJC Scopus subject areas

  • Cancer Research

引用此文

Areca nut-induced buccal mucosa fibroblast contraction and its signaling : A potential role in oral submucous fibrosis-a precancer condition. / Chang, Mei Chi; Lin, Li Deh; Wu, Hui Lin; Ho, Yuan Soon; Hsien, Hsiang Chi; Wang, Tong Mei; Jeng, Po Yuan; Cheng, Ru Hsiu; Hahn, Liang Jiunn; Jeng, Jiiang Huei.

於: Carcinogenesis, 卷 34, 編號 5, 05.2013, p. 1096-1104.

研究成果: 雜誌貢獻文章

Chang, MC, Lin, LD, Wu, HL, Ho, YS, Hsien, HC, Wang, TM, Jeng, PY, Cheng, RH, Hahn, LJ & Jeng, JH 2013, 'Areca nut-induced buccal mucosa fibroblast contraction and its signaling: A potential role in oral submucous fibrosis-a precancer condition', Carcinogenesis, 卷 34, 編號 5, 頁 1096-1104. https://doi.org/10.1093/carcin/bgt012
Chang, Mei Chi ; Lin, Li Deh ; Wu, Hui Lin ; Ho, Yuan Soon ; Hsien, Hsiang Chi ; Wang, Tong Mei ; Jeng, Po Yuan ; Cheng, Ru Hsiu ; Hahn, Liang Jiunn ; Jeng, Jiiang Huei. / Areca nut-induced buccal mucosa fibroblast contraction and its signaling : A potential role in oral submucous fibrosis-a precancer condition. 於: Carcinogenesis. 2013 ; 卷 34, 編號 5. 頁 1096-1104.
@article{e5876e8e8f804dd0b6b0ca8047d3f5b9,
title = "Areca nut-induced buccal mucosa fibroblast contraction and its signaling: A potential role in oral submucous fibrosis-a precancer condition",
abstract = "Betel quid (BQ) chewing is an oral habit that increases the risk of oral cancer and oral submucous fibrosis (OSF), a precancerous condition showing epithelial atrophy and tissue fibrosis. Persistent fibroblast contraction may induce the fibrotic contracture of tissue. In this study, we found that areca nut extract (ANE) (200-1200 μg/ ml) stimulated buccal mucosa fibroblast (OMF)-populated collagen gel contraction. Arecoline but not arecaidine-two areca alkaloids, slightly induced the OMF contraction. Exogenous addition of carboxylesterase (2 U/ml) prevented the arecoline- but not ANEinduced OMF contraction. OMF expressed inositol triphosphate (IP3) receptors. ANE-induced OMF (800 μg/ml) contraction was inhibited by U73122 [phospholipase C (PLC) inhibitor] and 2-aminoethoxydiphenyl borate (IP3 receptor antagonist), respectively. Ethylene glycol tetraacetic acid and verapamil, two calcium mobilization modulators, also suppressed the ANE-induced OMF contraction. ANE induced calcium/calmodulin kinase II and myosin light chain (MLC) phosphorylation in OMF. Moreover, W7 (a Ca2+/ calmodulin inhibitor), HA1077 (Rho kinase inhibitor), ML-7 (MLC kinase inhibitor) and cytochalasin B (actin filament polymerization inhibitor) inhibited the ANE-induced OMF contraction. Although ANE elevated reactive oxygen species (ROS) level in OMF, catalase, superoxide dismutase and N-acetyl-l-cysteine showed no obvious effect on ANE-elicited OMF contraction. These results indicate that BQ chewing may affect the wound healing and fibrotic processes in OSF via inducing OMF contraction by ANE and areca alkaloids. AN components-induced OMF contraction was related to PLC/ IP3/Ca2+/calmodulin and Rho signaling pathway as well as actin filament polymerization, but not solely due to ROS production.",
author = "Chang, {Mei Chi} and Lin, {Li Deh} and Wu, {Hui Lin} and Ho, {Yuan Soon} and Hsien, {Hsiang Chi} and Wang, {Tong Mei} and Jeng, {Po Yuan} and Cheng, {Ru Hsiu} and Hahn, {Liang Jiunn} and Jeng, {Jiiang Huei}",
year = "2013",
month = "5",
doi = "10.1093/carcin/bgt012",
language = "English",
volume = "34",
pages = "1096--1104",
journal = "Carcinogenesis",
issn = "0143-3334",
publisher = "Oxford University Press",
number = "5",

}

TY - JOUR

T1 - Areca nut-induced buccal mucosa fibroblast contraction and its signaling

T2 - A potential role in oral submucous fibrosis-a precancer condition

AU - Chang, Mei Chi

AU - Lin, Li Deh

AU - Wu, Hui Lin

AU - Ho, Yuan Soon

AU - Hsien, Hsiang Chi

AU - Wang, Tong Mei

AU - Jeng, Po Yuan

AU - Cheng, Ru Hsiu

AU - Hahn, Liang Jiunn

AU - Jeng, Jiiang Huei

PY - 2013/5

Y1 - 2013/5

N2 - Betel quid (BQ) chewing is an oral habit that increases the risk of oral cancer and oral submucous fibrosis (OSF), a precancerous condition showing epithelial atrophy and tissue fibrosis. Persistent fibroblast contraction may induce the fibrotic contracture of tissue. In this study, we found that areca nut extract (ANE) (200-1200 μg/ ml) stimulated buccal mucosa fibroblast (OMF)-populated collagen gel contraction. Arecoline but not arecaidine-two areca alkaloids, slightly induced the OMF contraction. Exogenous addition of carboxylesterase (2 U/ml) prevented the arecoline- but not ANEinduced OMF contraction. OMF expressed inositol triphosphate (IP3) receptors. ANE-induced OMF (800 μg/ml) contraction was inhibited by U73122 [phospholipase C (PLC) inhibitor] and 2-aminoethoxydiphenyl borate (IP3 receptor antagonist), respectively. Ethylene glycol tetraacetic acid and verapamil, two calcium mobilization modulators, also suppressed the ANE-induced OMF contraction. ANE induced calcium/calmodulin kinase II and myosin light chain (MLC) phosphorylation in OMF. Moreover, W7 (a Ca2+/ calmodulin inhibitor), HA1077 (Rho kinase inhibitor), ML-7 (MLC kinase inhibitor) and cytochalasin B (actin filament polymerization inhibitor) inhibited the ANE-induced OMF contraction. Although ANE elevated reactive oxygen species (ROS) level in OMF, catalase, superoxide dismutase and N-acetyl-l-cysteine showed no obvious effect on ANE-elicited OMF contraction. These results indicate that BQ chewing may affect the wound healing and fibrotic processes in OSF via inducing OMF contraction by ANE and areca alkaloids. AN components-induced OMF contraction was related to PLC/ IP3/Ca2+/calmodulin and Rho signaling pathway as well as actin filament polymerization, but not solely due to ROS production.

AB - Betel quid (BQ) chewing is an oral habit that increases the risk of oral cancer and oral submucous fibrosis (OSF), a precancerous condition showing epithelial atrophy and tissue fibrosis. Persistent fibroblast contraction may induce the fibrotic contracture of tissue. In this study, we found that areca nut extract (ANE) (200-1200 μg/ ml) stimulated buccal mucosa fibroblast (OMF)-populated collagen gel contraction. Arecoline but not arecaidine-two areca alkaloids, slightly induced the OMF contraction. Exogenous addition of carboxylesterase (2 U/ml) prevented the arecoline- but not ANEinduced OMF contraction. OMF expressed inositol triphosphate (IP3) receptors. ANE-induced OMF (800 μg/ml) contraction was inhibited by U73122 [phospholipase C (PLC) inhibitor] and 2-aminoethoxydiphenyl borate (IP3 receptor antagonist), respectively. Ethylene glycol tetraacetic acid and verapamil, two calcium mobilization modulators, also suppressed the ANE-induced OMF contraction. ANE induced calcium/calmodulin kinase II and myosin light chain (MLC) phosphorylation in OMF. Moreover, W7 (a Ca2+/ calmodulin inhibitor), HA1077 (Rho kinase inhibitor), ML-7 (MLC kinase inhibitor) and cytochalasin B (actin filament polymerization inhibitor) inhibited the ANE-induced OMF contraction. Although ANE elevated reactive oxygen species (ROS) level in OMF, catalase, superoxide dismutase and N-acetyl-l-cysteine showed no obvious effect on ANE-elicited OMF contraction. These results indicate that BQ chewing may affect the wound healing and fibrotic processes in OSF via inducing OMF contraction by ANE and areca alkaloids. AN components-induced OMF contraction was related to PLC/ IP3/Ca2+/calmodulin and Rho signaling pathway as well as actin filament polymerization, but not solely due to ROS production.

UR - http://www.scopus.com/inward/record.url?scp=84877592734&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=84877592734&partnerID=8YFLogxK

U2 - 10.1093/carcin/bgt012

DO - 10.1093/carcin/bgt012

M3 - Article

C2 - 23349021

AN - SCOPUS:84877592734

VL - 34

SP - 1096

EP - 1104

JO - Carcinogenesis

JF - Carcinogenesis

SN - 0143-3334

IS - 5

ER -