EXPRESSION OF EPIDERMAL GROWTH-FACTOR, TRANSFORMING GROWTH FACTOR-ALPHA AND THEIR RECEPTOR IN GASTROESOPHAGEAL DISEASES

被引:34
作者
JANKOWSKI, J
HOPWOOD, D
WORMSLEY, KG
机构
[1] Gastrointestinal Unit, Department of Medicine, London, Lincoln’s Inn Fields
[2] Department of Pathology, University of Dundee, London, Lincoln’s Inn Fields
[3] Histopathology Unit, Imperial Cancer Research Fund, London, Lincoln’s Inn Fields
关键词
BARRETTS ESOPHAGUS; EPIDERMAL GROWTH FACTOR; EPIDERMAL GROWTH FACTOR RECEPTOR; ESOPHAGITIS; ESOPHAGEAL CANCER; GASTRITIS; GASTRIC CANCER; TRANSFORMING GROWTH-FACTOR-ALPHA;
D O I
10.1159/000171396
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
This article is a review of aspects of the expression of the regulatory peptides; epidermal growth factor (EGF), transforming growth factor alpha (TGF-alpha), and their receptor (EGF-R) in the epithelium of the human oesophagus and stomach in health and disease. It has become clear that TGF-alpha has increased expression in metaplastic, dysplastic and neoplastic tissue of the oesophagus compared with normal mucosa. The degree of abnormal expression becomes more marked as dysplasia increases. TGF-alpha expression is also increased in gastric neoplasias. EGF has a different pattern of expression, being decreased in oesophagitis and increased in gastritis. Although EGF is present in Barrett's oesophagitis, the expression of EGF does not discriminate between dysplastic and neoplastic epithelium. EGF-R is normally expressed on all gastro-intestinal epithelia, but its expression is increased in Barrett's epithelium, as well as in adenocarcinomas of the oesophagus and the stomach. The two peptides bind to their receptors on the mucosal cell membranes, and the co-expression of peptide and receptor is positively associated with varying degrees of cellular proliferation. The density of receptor expression may modulate the proliferative stimulus, leading to either mitogenic (regulated) or oncogenic (unregulated) growth.
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页码:1 / 11
页数:11
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共 80 条
[71]  
Hui W.M., Chen B.W., Cho C.H., Luk C.T., Lam S.K., The effect of epidermal growth factor (EGF) on gastric mucosal blood flow (abstract), Gastroenterology, 100, (1991)
[72]  
Chen M.C., Olson C., Tanner M, Soil AH: Apical EGF/TGF alpha receptors mediate enhanced resistance of gastric mucosal cell monolayers to apical acidification (abstract), Gastroenterology, 100, (1991)
[73]  
Hansson H.A., Hong L., Helander H.F., Changes in gastric EGF, EGF receptors and acidity during healing of gastric ulcer in the rat, Acta Physiol Scand, 138, (1990)
[74]  
Chernoff E.A., Robertson S., Epidermal growth factor and the onset of epithelial wound healing, Tissue Cell, 22, pp. 123-135, (1990)
[75]  
Di Marco E., Pierce J.H., Aaronson S.A., Di Fore P.P., Mechanisms by which EGF receptor and theTGFa contribute to malignant transformation, Nat Imniun Cell Growth Regul, 9, pp. 209-221, (1990)
[76]  
Anklesaria P., Teixido J., Laiho M., Pierce J.H., Greenberger J.S., Massa-Que J., Cell-cell adhesion mediated by binding of membrane-anchored transforming growth factor alpha to epidermal growth factor receptors promotes cell proliferation, Proc Natl Acad Sci USA, 87, pp. 3289-3293, (1990)
[77]  
West M.A., Bretscher M.S., Watts C., Distinct endocytotic pathways in epidermal growth factor-stimulated human carcinoma A341 cells, J Cell Biol, 109, pp. 2731-2739, (1989)
[78]  
Lai W.H., Cameron P.H., Wda I., Doherty J.J., Kay D.G., Posner B.I., Bergeron J.J.M., Ligand-mediated internalisation, recycling, and downregulation of the epidermal growth factor receptor in vivo, J Cell Biol, 109, pp. 2741-2749, (1989)
[79]  
Lott M., Wright N.A., Epithelial kinetics, control and consequences of alterations in disease, Gastrointestinal and Oesophageal Pathology, pp. 230-467, (1989)
[80]  
Tsoni P.A., Tsoni A.A., Chaos: Principles and implications in biology, Comput Appl Biosci, 5, pp. 27-32, (1989)