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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

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)...

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Autores principales: Ji, Wen-Tsai, Chuang, Yao-Chi, Chen, Han-Po, Lee, Ching-Chih, Chen, Jeff Yi-Fu, Yang, Sheng-Ru, Chen, Jung-Hua, Wang, Chun-Jen, Chen, Hau-Ren
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5598531/
https://www.ncbi.nlm.nih.gov/pubmed/28962320
http://dx.doi.org/10.1016/j.toxrep.2014.10.018
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author Ji, Wen-Tsai
Chuang, Yao-Chi
Chen, Han-Po
Lee, Ching-Chih
Chen, Jeff Yi-Fu
Yang, Sheng-Ru
Chen, Jung-Hua
Wang, Chun-Jen
Chen, Hau-Ren
author_facet Ji, Wen-Tsai
Chuang, Yao-Chi
Chen, Han-Po
Lee, Ching-Chih
Chen, Jeff Yi-Fu
Yang, Sheng-Ru
Chen, Jung-Hua
Wang, Chun-Jen
Chen, Hau-Ren
author_sort Ji, Wen-Tsai
collection PubMed
description 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.
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spelling pubmed-55985312017-09-28 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 Ji, Wen-Tsai Chuang, Yao-Chi Chen, Han-Po Lee, Ching-Chih Chen, Jeff Yi-Fu Yang, Sheng-Ru Chen, Jung-Hua Wang, Chun-Jen Chen, Hau-Ren Toxicol Rep Article 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. Elsevier 2014-11-04 /pmc/articles/PMC5598531/ /pubmed/28962320 http://dx.doi.org/10.1016/j.toxrep.2014.10.018 Text en © 2014 The Authors http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/3.0/).
spellingShingle Article
Ji, Wen-Tsai
Chuang, Yao-Chi
Chen, Han-Po
Lee, Ching-Chih
Chen, Jeff Yi-Fu
Yang, Sheng-Ru
Chen, Jung-Hua
Wang, Chun-Jen
Chen, Hau-Ren
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
title 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
title_full 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
title_fullStr 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
title_full_unstemmed 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
title_short 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
title_sort 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
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5598531/
https://www.ncbi.nlm.nih.gov/pubmed/28962320
http://dx.doi.org/10.1016/j.toxrep.2014.10.018
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