TY - JOUR
T1 - A novel dietary-related model of esophagitis and Barrett's esophagus, a premalignant lesion
AU - Guy, Naihsuan C.
AU - Garewal, Harinder
AU - Holubec, Hana
AU - Bernstein, Harris
AU - Payne, Claire M.
AU - Bernstein, Carol
AU - Bhattacharyya, Achyut K.
AU - Dvorak, Katerina
N1 - Funding Information:
This work was supported by grants from the Arizona Biomedical Research Commission Contract ID#0012 and from National Institute of Health and National Cancer Institute Grant 1 P50 CA95060 Specialized Program of Research Excellence (SPORE). Address correspondence to Katerina Dvorak, Department of Cell Biology and Anatomy, College of Medicine, University of Arizona, Tucson, AZ 85724. Phone: 520-626-3934. FAX: 520-626-2097. E-mail: [email protected].
PY - 2007
Y1 - 2007
N2 - Barrett's esophagus (BE) is a premalignant lesion in which columnar epithelium (containing goblet cells) replaces esophageal squamous cells. Previous evidence suggested that hydrophobic bile acids and zinc deficiency each play a role in BE development. We fed wild-type C57BL/6 mice a zinc-deficient diet containing the hydrophobic bile acid, deoxycholic acid for various times up to 152 days. All mice fed this diet developed esophagitis by 69 days on the diet and 63% of the mice on this diet for 88 to 152 days also developed a BE-like lesion. Esophageal tissues showed thickened mucosa, increased proliferation, and increased expression of markers associated with oxidative and nitrosative stress. The newly formed BE-like lesions expressed Mucin-2, a marker of columnar differentiation. They also showed translocation of the p65 subunit of nuclear factor-κB and β-catenin to the nucleus and typical histological changes associated with BE lesions. This mouse model of esophagitis and BE is expected to contribute to a deeper understanding of BE pathogenesis and to strategies for prevention of BE progression to cancer.
AB - Barrett's esophagus (BE) is a premalignant lesion in which columnar epithelium (containing goblet cells) replaces esophageal squamous cells. Previous evidence suggested that hydrophobic bile acids and zinc deficiency each play a role in BE development. We fed wild-type C57BL/6 mice a zinc-deficient diet containing the hydrophobic bile acid, deoxycholic acid for various times up to 152 days. All mice fed this diet developed esophagitis by 69 days on the diet and 63% of the mice on this diet for 88 to 152 days also developed a BE-like lesion. Esophageal tissues showed thickened mucosa, increased proliferation, and increased expression of markers associated with oxidative and nitrosative stress. The newly formed BE-like lesions expressed Mucin-2, a marker of columnar differentiation. They also showed translocation of the p65 subunit of nuclear factor-κB and β-catenin to the nucleus and typical histological changes associated with BE lesions. This mouse model of esophagitis and BE is expected to contribute to a deeper understanding of BE pathogenesis and to strategies for prevention of BE progression to cancer.
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U2 - 10.1080/01635580701499529
DO - 10.1080/01635580701499529
M3 - Article
C2 - 18001217
AN - SCOPUS:36849089128
SN - 0163-5581
VL - 59
SP - 217
EP - 227
JO - Nutrition and cancer
JF - Nutrition and cancer
IS - 2
ER -