Expression of E-cadherin in human epidermal non-melanoma cutaneous tumours

被引:44
作者
Fuller, LC [1 ]
Allen, MH [1 ]
Montesu, M [1 ]
Barker, JNWN [1 ]
Macdonald, DM [1 ]
机构
[1] UNITED MED & DENT SCH,GUYS & ST THOMAS HOSP,ST JOHNS INST DERMATOL,DUNHILL LAB,LONDON SE1 9RT,ENGLAND
关键词
D O I
10.1046/j.1365-2133.1996.d01-739.x
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
E-cadherin is a calcium-sensitive, cell-to-cell, adhesion molecule that is expressed widely in normal human epithelial tissue. abnormal expression has been described in colorectal, breast and nasopharyngeal squamous cell carcinomas, where loss of E-cadherin is associated with an increased metastatic potential. We have examined, by standard immunohistochemical techniques using the monoclonal antibody HECD-1 (E-cadherin monoclonal antibody), the distribution of E-cadherin in normal human skin and in non-melanoma neoplastic lesions. In the normal epidermis, E-cadherin was strongly expressed on the surface of keratinocytes and specialized epithelial structures. Staining was absent from the lower pole of basal keratinocytes in contact with the basement membrane. Weak cytoplasmic staining was also noted in basal keratinocytes. No reactivity was demonstrated in dermal structures. The assessment of cutaneous tumours demonstrated an altered pattern of staining in most cases. Cell surface expression was reduced in 28 of 30 cases of basal cell carcinomas (BCC). Twenty showed an additional feature of positive staining on the dermal aspect of peripheral cells of tumour lobules. In squamous cell carcinomas (SCC) (n = 16), surface expression was attenuated in eight and absent in a further four. Strong surface expression, similar to normal skin was seen in all examples of Bowen's disease (n = 6), viral wart (n = 3), seborrhoeic keratosis (n = 3) and actinic keratosis (n = 4). This study demonstrates that, in BCC and SCC, but not in premalignant lesions, cell-surface expression of E-cadherin is reduced, consistent with the observation that the loss of E-cadherin is associated with tumour invasion.
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页码:28 / 32
页数:5
相关论文
共 16 条
[1]   THE DEVELOPMENT OF A REPRODUCIBLE IMMUNOCYTOCHEMICAL TECHNIQUE FOR DEMONSTRATING COLOCALIZED CUTANEOUS ANTIGENS [J].
ALLEN, MH ;
MARKEY, AC ;
MACDONALD, DM .
AMERICAN JOURNAL OF DERMATOPATHOLOGY, 1991, 13 (03) :221-227
[2]   LOSS OF EPITHELIAL DIFFERENTIATION AND GAIN OF INVASIVENESS CORRELATES WITH TYROSINE PHOSPHORYLATION OF THE E-CADHERIN BETA-CATENIN COMPLEX IN CELLS TRANSFORMED WITH A TEMPERATURE-SENSITIVE V-SRC GENE [J].
BEHRENS, J ;
VAKAET, L ;
FRIIS, R ;
WINTERHAGER, E ;
VANROY, F ;
MAREEL, MM ;
BIRCHMEIER, W .
JOURNAL OF CELL BIOLOGY, 1993, 120 (03) :757-766
[3]   DISSOCIATION OF MADIN-DARBY CANINE KIDNEY EPITHELIAL-CELLS BY THE MONOCLONAL-ANTIBODY ANTI-ARC-1 - MECHANISTIC ASPECTS AND IDENTIFICATION OF THE ANTIGEN AS A COMPONENT RELATED TO UVOMORULIN [J].
BEHRENS, J ;
BIRCHMEIER, W ;
GOODMAN, SL ;
IMHOF, BA .
JOURNAL OF CELL BIOLOGY, 1985, 101 (04) :1307-1315
[4]   HUMAN CELL-ADHESION MOLECULE UVOMORULIN IS DIFFERENTIALLY EXPRESSED IN VARIOUS SKIN TUMORS [J].
CZECH, W ;
KRUTMANN, J ;
HERRENKNECHT, K ;
SCHOPF, E ;
KAPP, A .
JOURNAL OF CUTANEOUS PATHOLOGY, 1993, 20 (02) :168-172
[5]   IDENTIFICATION AND PURIFICATION OF A CELL-SURFACE GLYCOPROTEIN MEDIATING INTERCELLULAR-ADHESION IN EMBRYONIC AND ADULT TISSUE [J].
DAMSKY, CH ;
RICHA, J ;
SOLTER, D ;
KNUDSEN, K ;
BUCK, CA .
CELL, 1983, 34 (02) :455-466
[6]  
DORUDI S, 1993, AM J PATHOL, V142, P981
[7]   E-CADHERIN-MEDIATED CELL CELL-ADHESION PREVENTS INVASIVENESS OF HUMAN CARCINOMA-CELLS [J].
FRIXEN, UH ;
BEHRENS, J ;
SACHS, M ;
EBERLE, G ;
VOSS, B ;
WARDA, A ;
LOCHNER, D ;
BIRCHMEIER, W .
JOURNAL OF CELL BIOLOGY, 1991, 113 (01) :173-185
[8]   BIOLOGY OF TUMOR-METASTASIS [J].
HART, IR ;
SAINI, A .
LANCET, 1992, 339 (8807) :1453-1457
[9]   THE ROLE OF THE CELL-CELL ADHESION MOLECULE E-CADHERIN IN LARGE-BOWEL TUMOR-CELL INVASION AND METASTASIS [J].
KINSELLA, AR ;
GREEN, B ;
LEPTS, GC ;
HILL, CL ;
BOWIE, G ;
TAYLOR, BA .
BRITISH JOURNAL OF CANCER, 1993, 67 (05) :904-909
[10]  
MOLL R, 1993, AM J PATHOL, V143, P1731