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Influence of Tea Consumption on the Development of Second Esophageal Neoplasm in Patients with Head and Neck Cancer
Alcohol is an important risk factor for the development of second esophageal squamous-cell carcinoma (ESCC) in head and neck squamous-cell carcinoma (HNSCC) patients. However, the influence of tea consumption is uncertain. We prospectively performed endoscopic screening in incident HNSCC patients to...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6468666/ https://www.ncbi.nlm.nih.gov/pubmed/30893904 http://dx.doi.org/10.3390/cancers11030387 |
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author | Wang, Yao-Kuang Chen, Wei-Chung Lai, Ying-Ho Chen, Yi-Hsun Wu, Ming-Tsang Kuo, Chie-Tong Wang, Yen-Yun Yuan, Shyng-Shiou F. Liu, Yu-Peng Wu, I-Chen |
author_facet | Wang, Yao-Kuang Chen, Wei-Chung Lai, Ying-Ho Chen, Yi-Hsun Wu, Ming-Tsang Kuo, Chie-Tong Wang, Yen-Yun Yuan, Shyng-Shiou F. Liu, Yu-Peng Wu, I-Chen |
author_sort | Wang, Yao-Kuang |
collection | PubMed |
description | Alcohol is an important risk factor for the development of second esophageal squamous-cell carcinoma (ESCC) in head and neck squamous-cell carcinoma (HNSCC) patients. However, the influence of tea consumption is uncertain. We prospectively performed endoscopic screening in incident HNSCC patients to identify synchronous esophageal neoplasm. In total, 987 patients enrolled between October 2008 and December 2017 and were analyzed. In vitro studies were conducted to investigate the effect of epigallocatechin gallate (EGCG) on the betel alkaloid, arecoline-stimulated carcinogenesis in two ESCC cell lines. There were 151 patients (15.3%) diagnosed to have synchronous esophageal neoplasm, including 88 low-grade dysplasia, 30 high-grade dysplasia and 33 squamous-cell carcinoma (SCC). Tea consumption was associated with a significantly lower risk of having esophageal high-grade dysplasia or SCC in HNSCC patients, especially those who were betel nut chewers, alcohol drinkers or cigarette smokers (all adjusted odds ratio were 0.5; p-values: 0.045, 0.045 and 0.049 respectively). In vitro studies indicated that EGCG suppressed arecoline-induced ESCC cell proliferation and colony formation through the inhibition of the Akt and ERK1/2 pathway in a reactive oxygen species-independent manner. In conclusion, tea consumption may protect against the development of second esophageal neoplasms among HNSCC patients, especially those who regularly consume betel nuts, alcohol and cigarettes. |
format | Online Article Text |
id | pubmed-6468666 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-64686662019-04-24 Influence of Tea Consumption on the Development of Second Esophageal Neoplasm in Patients with Head and Neck Cancer Wang, Yao-Kuang Chen, Wei-Chung Lai, Ying-Ho Chen, Yi-Hsun Wu, Ming-Tsang Kuo, Chie-Tong Wang, Yen-Yun Yuan, Shyng-Shiou F. Liu, Yu-Peng Wu, I-Chen Cancers (Basel) Article Alcohol is an important risk factor for the development of second esophageal squamous-cell carcinoma (ESCC) in head and neck squamous-cell carcinoma (HNSCC) patients. However, the influence of tea consumption is uncertain. We prospectively performed endoscopic screening in incident HNSCC patients to identify synchronous esophageal neoplasm. In total, 987 patients enrolled between October 2008 and December 2017 and were analyzed. In vitro studies were conducted to investigate the effect of epigallocatechin gallate (EGCG) on the betel alkaloid, arecoline-stimulated carcinogenesis in two ESCC cell lines. There were 151 patients (15.3%) diagnosed to have synchronous esophageal neoplasm, including 88 low-grade dysplasia, 30 high-grade dysplasia and 33 squamous-cell carcinoma (SCC). Tea consumption was associated with a significantly lower risk of having esophageal high-grade dysplasia or SCC in HNSCC patients, especially those who were betel nut chewers, alcohol drinkers or cigarette smokers (all adjusted odds ratio were 0.5; p-values: 0.045, 0.045 and 0.049 respectively). In vitro studies indicated that EGCG suppressed arecoline-induced ESCC cell proliferation and colony formation through the inhibition of the Akt and ERK1/2 pathway in a reactive oxygen species-independent manner. In conclusion, tea consumption may protect against the development of second esophageal neoplasms among HNSCC patients, especially those who regularly consume betel nuts, alcohol and cigarettes. MDPI 2019-03-19 /pmc/articles/PMC6468666/ /pubmed/30893904 http://dx.doi.org/10.3390/cancers11030387 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Wang, Yao-Kuang Chen, Wei-Chung Lai, Ying-Ho Chen, Yi-Hsun Wu, Ming-Tsang Kuo, Chie-Tong Wang, Yen-Yun Yuan, Shyng-Shiou F. Liu, Yu-Peng Wu, I-Chen Influence of Tea Consumption on the Development of Second Esophageal Neoplasm in Patients with Head and Neck Cancer |
title | Influence of Tea Consumption on the Development of Second Esophageal Neoplasm in Patients with Head and Neck Cancer |
title_full | Influence of Tea Consumption on the Development of Second Esophageal Neoplasm in Patients with Head and Neck Cancer |
title_fullStr | Influence of Tea Consumption on the Development of Second Esophageal Neoplasm in Patients with Head and Neck Cancer |
title_full_unstemmed | Influence of Tea Consumption on the Development of Second Esophageal Neoplasm in Patients with Head and Neck Cancer |
title_short | Influence of Tea Consumption on the Development of Second Esophageal Neoplasm in Patients with Head and Neck Cancer |
title_sort | influence of tea consumption on the development of second esophageal neoplasm in patients with head and neck cancer |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6468666/ https://www.ncbi.nlm.nih.gov/pubmed/30893904 http://dx.doi.org/10.3390/cancers11030387 |
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