1.Expression of MUC3, MUC5AC, MUC6 and Epidermal Growth Factor Receptor in Gallbladder Epithelium according to Gallstone Composition.
Hyo Jung KIM ; Jae Seon KIM ; Kyoung Oh KIM ; Ki Ho PARK ; Hyung Joon YIM ; Jin Yong KIM ; Jong Eun YEON ; Jong Jae PARK ; Jae Jeong SHIM ; Kwan Soo BYUN ; Young Tae BAK ; Chang Hong LEE
The Korean Journal of Gastroenterology 2003;42(4):330-336
BACKGROUND/AIMS: Gallbladder (GB) mucin is one of the key factors in the gallstone formation. However, there is little information about the diversity of mucin secretion according to the stone composition. Epidermal growth factor receptor (EGFR) functions in proliferation including mucin secreting goblet cell hyperplasia. We compared the expressions of MUC3, MUC5AC, MUC6 and EGFR in the GB epithelium with cholesterol gallstones (GB-chol) group and pigment gallstones (GB-pig group). METHODS: GBs from elective laparoscopic cholecystectomy for the gallstone disease were studied. Stone composition was analyzed by the spectrophotometer. Immunohistochemical stain was performed using each monoclonal antibody. The percentage of stained proportion was scored by the NIH image program and the results were compared between both groups. RESULTS: Total 20 patients were enrolled (10 patients with cholesterol gallstones, 10 patients with pigment gallstones). The percentages of stained proportion for MUC3, MUC5AC, and MUC6 were 42+/-27%, 31+/-15%, and 17+/-9%, respectively in GB-chol group and 32+/-22%, 33+/-23%, and 15+/-10%, respectively in GB-pig group (p>0.05). The expression of EGFR was 50% (5/10) in the GB-chol group and 80% (8/10) in the GB-pig group respectively. CONCLUSIONS: There was no difference in the expressions of MUC3, MUC5AC, and MUC6 between the two groups. Further studies are needed to elucidate the role of EGFR in the gallstore formation.
Bile Pigments/analysis
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Cholelithiasis/chemistry/*metabolism
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Cholesterol/analysis
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Epithelium/metabolism
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Gallbladder/*metabolism
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Humans
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Immunohistochemistry
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Mucin 5AC
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Mucin-3
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Mucin-6
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Mucins/*analysis
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Receptor, Epidermal Growth Factor/*analysis
2.Mucin profile of the pancreatic mucinous cystic neoplasms.
Yuan JI ; Jian-fang XU ; Tian-tao KUANG ; Yan-nan ZHOU ; Shao-hua LU ; Yun-shan TAN
Chinese Medical Journal 2006;119(4):328-330
Adult
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Aged
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Female
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Humans
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Immunohistochemistry
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Male
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Middle Aged
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Mucin-2
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Mucin-6
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Mucins
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analysis
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Neoplasms, Cystic, Mucinous, and Serous
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chemistry
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Pancreatic Neoplasms
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chemistry
3.An Inverse Relationship between the Expression of the Gastric Tumor Suppressor RUNX3 and Infection with Helicobacter pylori in Gastric Epithelial Dysplasia.
Woo Chul CHUNG ; Sung Hoon JUNG ; Kyu Re JOO ; Min Ji KIM ; Gun Jung YOUN ; Yaeni KIM ; Joune Seup LEE ; Hyewon LEE ; Ji Han JUNG ; Yun Kyung LEE
Gut and Liver 2013;7(6):688-695
BACKGROUND/AIMS: This study was performed to determine the association between RUNX3 expression and Helicobacter pylori infection in premalignant gastric lesions. METHODS: We examined 107 patients with gastric epithelial dysplasia who had undergone endoscopic mucosal resection or submucosal dissection. All tissue samples were evaluated by RUNX3 staining and subclassified by immunophenotype. H. pylori infection in dysplastic lesions and the normal surrounding tissue was examined by silver staining, and cagA status was assessed by polymerase chain reaction. RESULTS: The loss of RUNX3 expression was observed in 62 cases (57.9%), and an association with H. pylori infection was found in 54 cases (50.5%). The infection rate with the cagA-positive H. pylori strain was 63.0%. In RUNX3-negative lesions, the rate of H. pylori infection (p=0.03) and the frequency of category 4 lesions (according to the revised Vienna classification) were high (p=0.02). In addition, the gastric mucin phenotype was predominant. In RUNX3-negative category 4 lesions, the rate of cagA-positive H. pylori infection rate was high but not significantly increased (p=0.08). CONCLUSIONS: Infection with H. pylori is associated with inactivation of RUNX3 in early gastric carcinogenesis. This mechanism was prominent in gastric cancer with a gastric mucin phenotype.
Adenoma/*chemistry
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Aged
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Antigens, Bacterial/genetics
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Bacterial Proteins/genetics
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Carcinoma/*chemistry
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Cell Transformation, Neoplastic
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Core Binding Factor Alpha 3 Subunit/*analysis
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Female
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Gastric Mucosa/*chemistry/pathology
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Helicobacter Infections/*metabolism
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Helicobacter pylori/*genetics
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Humans
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Male
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Middle Aged
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Mucin 5AC/analysis
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Mucin-2/analysis
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Mucin-6/analysis
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Neprilysin/analysis
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Phenotype
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Precancerous Conditions/*chemistry/pathology
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Stomach Neoplasms/*chemistry