DUOX2 Expression Is Increased in Barrett Esophagus and Cancerous Tissues of Stomach and Colon

Aim. To detect the expression of dual oxidase (DUOX) 2 in Barrett esophagus, gastric cancer, and colorectal cancer (CRC). Materials and Methods. The endoscopic biopsies were collected from patients with Barrett esophagus, while the curative resection tissues were obtained from patients with gastric...

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Main Authors: Ran Qi, Yunfeng Zhou, Xiaozhen Li, Hong Guo, Lei Gao, Lijuan Wu, Yufeng Wang, Qiang Gao
Format: Article
Language:English
Published: Hindawi Limited 2016-01-01
Series:Gastroenterology Research and Practice
Online Access:http://dx.doi.org/10.1155/2016/1835684
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spelling doaj-b77613fe72184992af53ce22379a91412020-11-24T23:20:21ZengHindawi LimitedGastroenterology Research and Practice1687-61211687-630X2016-01-01201610.1155/2016/18356841835684DUOX2 Expression Is Increased in Barrett Esophagus and Cancerous Tissues of Stomach and ColonRan Qi0Yunfeng Zhou1Xiaozhen Li2Hong Guo3Lei Gao4Lijuan Wu5Yufeng Wang6Qiang Gao7Department of Gastroenterology and Hepatology, The First Affiliated Hospital, Henan University of Science and Technology, Luoyang, Henan 471000, ChinaShenzhen University Health Science Center, Shenzhen, Guangdong, ChinaDepartment of Gastroenterology and Hepatology, The First Affiliated Hospital, Henan University of Science and Technology, Luoyang, Henan 471000, ChinaDepartment of Gastroenterology and Hepatology, The First Affiliated Hospital, Henan University of Science and Technology, Luoyang, Henan 471000, ChinaDepartment of Gastroenterology and Hepatology, The First Affiliated Hospital, Henan University of Science and Technology, Luoyang, Henan 471000, ChinaDepartment of Gastroenterology and Hepatology, The First Affiliated Hospital, Henan University of Science and Technology, Luoyang, Henan 471000, ChinaDepartment of Gastroenterology and Hepatology, The First Affiliated Hospital, Henan University of Science and Technology, Luoyang, Henan 471000, ChinaDepartment of Gastroenterology and Hepatology, The First Affiliated Hospital, Henan University of Science and Technology, Luoyang, Henan 471000, ChinaAim. To detect the expression of dual oxidase (DUOX) 2 in Barrett esophagus, gastric cancer, and colorectal cancer (CRC). Materials and Methods. The endoscopic biopsies were collected from patients with Barrett esophagus, while the curative resection tissues were obtained from patients with gastric cancer, CRC, or hepatic carcinoma. The DUOX2 protein and mRNA levels were detected with immunohistochemistry (IHC) and real-time quantitative PCR (qPCR). The correlation of DUOX2 expression with clinicopathological parameters of tumors was identified. Results. Low levels of DUOX2 mRNA were detected in Barrett esophagus and the adjacent normal tissues, and there was no difference between these two groups. DUOX2 protein was found in Barrett esophagus and undetectable in the normal epithelium. The DUOX2 mRNA and protein levels in the gastric cancer and CRC were increased compared to the adjacent nonmalignant tissues. The elevated DUOX2 in the gastric cancer was significantly associated with smoking history. In CRC tissues, the DUOX2 protein expression level in stages II–IV was significantly higher than that in stage I. In both hepatic carcinoma and the adjacent nonmalignant tissue, the DUOX2 was virtually undetectable. Conclusion. DUOX2 in Barrett esophagus, gastric cancer, and CRC may be involved in the tumorigenesis of these tissues.http://dx.doi.org/10.1155/2016/1835684
collection DOAJ
language English
format Article
sources DOAJ
author Ran Qi
Yunfeng Zhou
Xiaozhen Li
Hong Guo
Lei Gao
Lijuan Wu
Yufeng Wang
Qiang Gao
spellingShingle Ran Qi
Yunfeng Zhou
Xiaozhen Li
Hong Guo
Lei Gao
Lijuan Wu
Yufeng Wang
Qiang Gao
DUOX2 Expression Is Increased in Barrett Esophagus and Cancerous Tissues of Stomach and Colon
Gastroenterology Research and Practice
author_facet Ran Qi
Yunfeng Zhou
Xiaozhen Li
Hong Guo
Lei Gao
Lijuan Wu
Yufeng Wang
Qiang Gao
author_sort Ran Qi
title DUOX2 Expression Is Increased in Barrett Esophagus and Cancerous Tissues of Stomach and Colon
title_short DUOX2 Expression Is Increased in Barrett Esophagus and Cancerous Tissues of Stomach and Colon
title_full DUOX2 Expression Is Increased in Barrett Esophagus and Cancerous Tissues of Stomach and Colon
title_fullStr DUOX2 Expression Is Increased in Barrett Esophagus and Cancerous Tissues of Stomach and Colon
title_full_unstemmed DUOX2 Expression Is Increased in Barrett Esophagus and Cancerous Tissues of Stomach and Colon
title_sort duox2 expression is increased in barrett esophagus and cancerous tissues of stomach and colon
publisher Hindawi Limited
series Gastroenterology Research and Practice
issn 1687-6121
1687-630X
publishDate 2016-01-01
description Aim. To detect the expression of dual oxidase (DUOX) 2 in Barrett esophagus, gastric cancer, and colorectal cancer (CRC). Materials and Methods. The endoscopic biopsies were collected from patients with Barrett esophagus, while the curative resection tissues were obtained from patients with gastric cancer, CRC, or hepatic carcinoma. The DUOX2 protein and mRNA levels were detected with immunohistochemistry (IHC) and real-time quantitative PCR (qPCR). The correlation of DUOX2 expression with clinicopathological parameters of tumors was identified. Results. Low levels of DUOX2 mRNA were detected in Barrett esophagus and the adjacent normal tissues, and there was no difference between these two groups. DUOX2 protein was found in Barrett esophagus and undetectable in the normal epithelium. The DUOX2 mRNA and protein levels in the gastric cancer and CRC were increased compared to the adjacent nonmalignant tissues. The elevated DUOX2 in the gastric cancer was significantly associated with smoking history. In CRC tissues, the DUOX2 protein expression level in stages II–IV was significantly higher than that in stage I. In both hepatic carcinoma and the adjacent nonmalignant tissue, the DUOX2 was virtually undetectable. Conclusion. DUOX2 in Barrett esophagus, gastric cancer, and CRC may be involved in the tumorigenesis of these tissues.
url http://dx.doi.org/10.1155/2016/1835684
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