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Differential expression of laminin-5 subunits and integrin receptors in human colorectal neoplasia
被引:0
|作者:
Sordat, I
Bosman, FT
Dorta, G
Rousselle, P
Aberdam, D
Blum, AL
Sordat, B
[1
]
机构:
[1] Swiss Inst Expt Canc Res, CH-1066 Epalinges, Switzerland
[2] CHU Vaudois, Univ Hosp, Inst Pathol, CH-1011 Lausanne, Switzerland
[3] CHU Vaudois, Univ Hosp, Div Gastroenterol, CH-1011 Lausanne, Switzerland
[4] Inst Biol & Chim Prot, CNRS, UPR 412, F-69367 Lyon 07, France
[5] Univ Nice, INSERM, U385, F-06034 Nice, France
来源:
关键词:
laminin-5;
integrins;
colorectal;
carcinogenesis;
D O I:
10.1002/(SICI)1096-9896(199805)185:1<44::AID-PATH46>3.0.CO;2-A
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
Cell-matrix interactions contribute to regulating the adhesion, growth, migration, and differentiation of epithelial intestinal cells. Alterations in matrix components and their cellular receptors have been found in tumours but their specific roles remain unclear. The tissue patterns of laminin-5 and alpha 3, beta 3 and gamma 2 subunits, as well as those of the alpha 3, alpha 6, beta 1, and beta 4 integrin chains, were determined by immunofluorescence on frozen sections of 12 colorectal mucosal samples from four patients, 15 adenomas, 29 adenocarcinomas, and eight metastases. Distinct patterns of laminin-5 and integrin expression were found along the mucosa-adenoma and adenoma-carcinoma transitions. Expression of basement membrane laminin-5 and submits was continuous and gradient-like in normal mucosa, enhanced at the periphery of adenomas, and discontinuous in places in carcinomas and metastases. Decrease of the alpha 3 integrin chain was found in adenomas, together with that of alpha 6 and beta 4 chains in carcinomas. A subpopulation of carcinoma cells dissociating (budding) from neoplastic tubules was found to accumulate the laminin-5 beta 3 gamma 2 heterodimer in the cytoplasm, with progressive loss of surface integrin expression. These results suggest that in colorectal cancer, an abnormal expression of laminin-5 subunits and integrin chains may identify a subset of carcinoma cells prone to invade focally and to contribute to disease aggressiveness. (C) 1998 John Wiley & Sons, Ltd.
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页码:44 / 52
页数:9
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