Literature DB >> 17070098

Areca nut extract treatment down-regulates involucrin in normal human oral keratinocyte through P13K/AKT activation.

Yu-Hsin Tseng1, Che-Shoa Chang, Tsung-Yun Liu, Shou-Yen Kao, Kuo-Wei Chang, Shu-Chun Lin.   

Abstract

Areca (betel) is an important etiological factor linked to the high prevalence of oral carcinoma and other oral diseases in South Asians. Involucrin is a key component of the cornified envelop and a differentiation marker of keratinocyte. In this study, we found that 5 microg/ml non-toxic areca nut extract (ANE) treatment resulted in the 0.5-fold down-regulation of involucrin and disruption in involucrin distribution in normal human oral keratinocyte (NHOK). Progressive down-regulation of involucrin during oral carcinogenesis was noted. Activation of AKT by 1.7-fold and up-regulation of COX-2 by 2-fold were elicited following ANE treatment in NHOK. Treatment with PI3K/AKT blockers reverted the down-regulation of involucrin. ANE also down-regulated involucrin by 0.6-fold and disturbed both cornified envelope and cell aggregation in calcium-induced differentiated NHOK. However, such phenomena seemed to be independent from the ANE-associated COX-2 activation. The ANE-associated down-regulation of involucrin through AKT pathway could underlie the areca-associated epithelial pathogenesis.

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Year:  2006        PMID: 17070098     DOI: 10.1016/j.oraloncology.2006.08.003

Source DB:  PubMed          Journal:  Oral Oncol        ISSN: 1368-8375            Impact factor:   5.337


  7 in total

1.  Stress activated p38 MAPK regulates cell cycle via AP-1 factors in areca extract exposed human lung epithelial cells.

Authors:  Rashmi Nagesh; K M Kiran Kumar; M Naveen Kumar; Rajeshwari H Patil; S Chidananda Sharma
Journal:  Cytotechnology       Date:  2019-02-02       Impact factor: 2.058

2.  Areca nut components stimulate ADAM17, IL-1α, PGE2 and 8-isoprostane production in oral keratinocyte: role of reactive oxygen species, EGF and JAK signaling.

Authors:  Mei-Chi Chang; Chiu-Po Chan; Yi-Jane Chen; Hsiang-Chi Hsien; Ya-Ching Chang; Sin-Yuet Yeung; Po-Yuan Jeng; Ru-Hsiu Cheng; Liang-Jiunn Hahn; Jiiang-Huei Jeng
Journal:  Oncotarget       Date:  2016-03-29

3.  Inhibition of Tanshinone IIA, salvianolic acid A and salvianolic acid B on Areca nut extract-induced oral submucous fibrosis in vitro.

Authors:  Jian-Ping Dai; Dan-Xia Zhu; Jiang-Tao Sheng; Xiao-Xuan Chen; Wei-Zhong Li; Ge-Fei Wang; Kang-Sheng Li; Yun Su
Journal:  Molecules       Date:  2015-04-15       Impact factor: 4.411

Review 4.  Multifaceted Mechanisms of Areca Nuts in Oral Carcinogenesis: the Molecular Pathology from Precancerous Condition to Malignant Transformation.

Authors:  Yi-Chen Li; Ann-Joy Cheng; Li-Yu Lee; Yu-Chen Huang; Joseph Tung-Chieh Chang
Journal:  J Cancer       Date:  2019-07-08       Impact factor: 4.207

Review 5.  Association of betel nut with carcinogenesis: revisit with a clinical perspective.

Authors:  Rajeshwar N Sharan; Ravi Mehrotra; Yashmin Choudhury; Kamlesh Asotra
Journal:  PLoS One       Date:  2012-08-13       Impact factor: 3.240

6.  Areca nut components affect COX-2, cyclin B1/cdc25C and keratin expression, PGE2 production in keratinocyte is related to reactive oxygen species, CYP1A1, Src, EGFR and Ras signaling.

Authors:  Mei-Chi Chang; Yi-Jane Chen; Hsiao-Hua Chang; Chiu-Po Chan; Chien-Yang Yeh; Yin-Lin Wang; Ru-Hsiu Cheng; Liang-Jiunn Hahn; Jiiang-Huei Jeng
Journal:  PLoS One       Date:  2014-07-22       Impact factor: 3.240

7.  Stimulation of MMP-9 of oral epithelial cells by areca nut extract is related to TGF-β/Smad2-dependent and -independent pathways and prevented by betel leaf extract, hydroxychavicol and melatonin.

Authors:  Mei-Chi Chang; Yu-Hwa Pan; Hsyueh-Liang Wu; Yi-Jie Lu; Wan-Chuen Liao; Chien-Yang Yeh; Jang-Jaer Lee; Jiiang-Huei Jeng
Journal:  Aging (Albany NY)       Date:  2019-12-12       Impact factor: 5.682

  7 in total

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