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Areca nut extracts exert different effects in oral cancer cells depending on serum concentration: A clue to the various oral alterations in betel quid chewers.

Authors :
Ji WT
Chuang YC
Chen HP
Lee CC
Chen JY
Yang SR
Chen JH
Wang CJ
Chen HR
Source :
Toxicology reports [Toxicol Rep] 2014 Nov 04; Vol. 1, pp. 1087-1095. Date of Electronic Publication: 2014 Nov 04 (Print Publication: 2014).
Publication Year :
2014

Abstract

Betel quid chewing is associated with various pathologic alterations in oral mucosa. However, the molecular mechanism behind so many contradictory alterations remains unclear. Here we aimed to build a model to facilitate the related studies in cultured cells. In our results, areca nut extract (ANE) was found to exert different effects in oral cells depending on the supplemented serum level. ANE strongly induced DNA damage, necrotic ballooning, and inflammatory cytokines under lower serum concentration while might convert to facilitate deregulated growth of serum-supplemented cells via modulating the activity/expression of factors such as E-cadherin and Snail. Despite ANE significantly activated NF-κB, a mediator critical for inflammation, inhibition of NF-κB did not prevent the activation of IL8 promoter. We further discovered Y705-dephosphorylated STAT3 might enhance IL8 transcription. Since necrosis and the inflammatory cytokines could cause massive inflammation, infiltration of interstitial fluid might potentiate cellular resistance against the acute cytotoxicity of ANE and further support the proliferation of transforming cells. Induction of VEGF and angiogenesis under lower serum condition also paved the way for cell growth and subsequent metastasis. Accordingly, we concluded that in correlation with serum infiltration ANE caused particular effects in oral cells and possibly the various clinicopathological alterations in vivo.

Details

Language :
English
ISSN :
2214-7500
Volume :
1
Database :
MEDLINE
Journal :
Toxicology reports
Publication Type :
Academic Journal
Accession number :
28962320
Full Text :
https://doi.org/10.1016/j.toxrep.2014.10.018