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Betel nut chewing, oral premalignant lesions, and the oral microbiome

Oral cancers are attributed to a number of causal agents including tobacco, alcohol, human papillomavirus (HPV), and areca (betel) nut. Although betel nut chewing has been established as an independent cause of oral cancer, the mechanisms of carcinogenesis are poorly understood. An investigation was...

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Autores principales: Hernandez, Brenda Y., Zhu, Xuemei, Goodman, Marc T., Gatewood, Robert, Mendiola, Paul, Quinata, Katrina, Paulino, Yvette C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5321455/
https://www.ncbi.nlm.nih.gov/pubmed/28225785
http://dx.doi.org/10.1371/journal.pone.0172196
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author Hernandez, Brenda Y.
Zhu, Xuemei
Goodman, Marc T.
Gatewood, Robert
Mendiola, Paul
Quinata, Katrina
Paulino, Yvette C.
author_facet Hernandez, Brenda Y.
Zhu, Xuemei
Goodman, Marc T.
Gatewood, Robert
Mendiola, Paul
Quinata, Katrina
Paulino, Yvette C.
author_sort Hernandez, Brenda Y.
collection PubMed
description Oral cancers are attributed to a number of causal agents including tobacco, alcohol, human papillomavirus (HPV), and areca (betel) nut. Although betel nut chewing has been established as an independent cause of oral cancer, the mechanisms of carcinogenesis are poorly understood. An investigation was undertaken to evaluate the influence of betel nut chewing on the oral microbiome and oral premalignant lesions. Study participants were recruited from a dental clinic in Guam. Structured interviews and oral examinations were performed. Oral swabbing and saliva samples were evaluated by 454 pyrosequencing of the V3- V5 region of the 16S rRNA bacterial gene and genotyped for HPV. One hundred twenty-two adults were enrolled including 64 current betel nut chewers, 37 former chewers, and 21 with no history of betel nut use. Oral premalignant lesions, including leukoplakia and submucous fibrosis, were observed in 10 chewers. Within-sample bacterial diversity was significantly lower in long-term (≥10 years) chewers vs. never chewers and in current chewers with oral lesions vs. individuals without lesions. Between-sample bacterial diversity based on Unifrac distances significantly differed by chewing status and oral lesion status. Current chewers had significantly elevated levels of Streptococcus infantis and higher and lower levels of distinct taxa of the Actinomyces and Streptococcus genera. Long-term chewers had reduced levels of Parascardovia and Streptococcus. Chewers with oral lesions had significantly elevated levels of Oribacterium, Actinomyces, and Streptococcus, including Streptococcus anginosus. In multivariate analyses, controlling for smoking, oral HPV, S.anginosus, and S. infantis levels, current betel nut chewing remained the only predictor of oral premalignant lesions. Our study provides evidence that betel nut chewing alters the oral bacterial microbiome including that of chewers who develop oral premalignant lesions. Nonetheless, whether microbial changes are involved in betel nut-induced oral carcinogenesis is only speculative. Further research is needed to discern the clinical significance of an altered oral microbiome and the mechanisms of oral cancer development in betel nut chewers.
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spelling pubmed-53214552017-03-09 Betel nut chewing, oral premalignant lesions, and the oral microbiome Hernandez, Brenda Y. Zhu, Xuemei Goodman, Marc T. Gatewood, Robert Mendiola, Paul Quinata, Katrina Paulino, Yvette C. PLoS One Research Article Oral cancers are attributed to a number of causal agents including tobacco, alcohol, human papillomavirus (HPV), and areca (betel) nut. Although betel nut chewing has been established as an independent cause of oral cancer, the mechanisms of carcinogenesis are poorly understood. An investigation was undertaken to evaluate the influence of betel nut chewing on the oral microbiome and oral premalignant lesions. Study participants were recruited from a dental clinic in Guam. Structured interviews and oral examinations were performed. Oral swabbing and saliva samples were evaluated by 454 pyrosequencing of the V3- V5 region of the 16S rRNA bacterial gene and genotyped for HPV. One hundred twenty-two adults were enrolled including 64 current betel nut chewers, 37 former chewers, and 21 with no history of betel nut use. Oral premalignant lesions, including leukoplakia and submucous fibrosis, were observed in 10 chewers. Within-sample bacterial diversity was significantly lower in long-term (≥10 years) chewers vs. never chewers and in current chewers with oral lesions vs. individuals without lesions. Between-sample bacterial diversity based on Unifrac distances significantly differed by chewing status and oral lesion status. Current chewers had significantly elevated levels of Streptococcus infantis and higher and lower levels of distinct taxa of the Actinomyces and Streptococcus genera. Long-term chewers had reduced levels of Parascardovia and Streptococcus. Chewers with oral lesions had significantly elevated levels of Oribacterium, Actinomyces, and Streptococcus, including Streptococcus anginosus. In multivariate analyses, controlling for smoking, oral HPV, S.anginosus, and S. infantis levels, current betel nut chewing remained the only predictor of oral premalignant lesions. Our study provides evidence that betel nut chewing alters the oral bacterial microbiome including that of chewers who develop oral premalignant lesions. Nonetheless, whether microbial changes are involved in betel nut-induced oral carcinogenesis is only speculative. Further research is needed to discern the clinical significance of an altered oral microbiome and the mechanisms of oral cancer development in betel nut chewers. Public Library of Science 2017-02-22 /pmc/articles/PMC5321455/ /pubmed/28225785 http://dx.doi.org/10.1371/journal.pone.0172196 Text en © 2017 Hernandez et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Hernandez, Brenda Y.
Zhu, Xuemei
Goodman, Marc T.
Gatewood, Robert
Mendiola, Paul
Quinata, Katrina
Paulino, Yvette C.
Betel nut chewing, oral premalignant lesions, and the oral microbiome
title Betel nut chewing, oral premalignant lesions, and the oral microbiome
title_full Betel nut chewing, oral premalignant lesions, and the oral microbiome
title_fullStr Betel nut chewing, oral premalignant lesions, and the oral microbiome
title_full_unstemmed Betel nut chewing, oral premalignant lesions, and the oral microbiome
title_short Betel nut chewing, oral premalignant lesions, and the oral microbiome
title_sort betel nut chewing, oral premalignant lesions, and the oral microbiome
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5321455/
https://www.ncbi.nlm.nih.gov/pubmed/28225785
http://dx.doi.org/10.1371/journal.pone.0172196
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