EXPRESSION OF MARKERS OF DIFFERENTIATION IN NORMAL BRONCHIAL EPITHELIUM AND BRONCHIAL DYSPLASIA

Citation
N. Pendleton et al., EXPRESSION OF MARKERS OF DIFFERENTIATION IN NORMAL BRONCHIAL EPITHELIUM AND BRONCHIAL DYSPLASIA, Journal of pathology, 178(2), 1996, pp. 146-150
Citations number
26
Categorie Soggetti
Pathology
Journal title
ISSN journal
00223417
Volume
178
Issue
2
Year of publication
1996
Pages
146 - 150
Database
ISI
SICI code
0022-3417(1996)178:2<146:EOMODI>2.0.ZU;2-C
Abstract
Bronchial epithelial dysplasia is a non-invasive cellular change often associated with physical or chemical injury and considered a pre-neop lastic lesion in the formation of lung cancer. A series of 39 bronchia l dysplasias associated with both neoplastic and non-neoplastic lesion s mere assessed for expression of markers of differentiation by immuno cytochemistry and compared with samples of normal bronchial epithelium . The normal bronchial epithelium studied expressed cytokeratins (CKs) 4, 6, 7, 8, 18, and 19 in all cases; CK 13 in 13 cases; and peanut ag glutinin (PNA) in seven cases. Involucrin, CK 10, and CK 14 were not o bserved in the normal bronchial samples. In the dysplastic bronchial b iopsies, epithelial staining was observed with epithelial CKs 7, 8, 18 , and 19 in all cases; CK 13 was seen in 26 cases; CK 14 in 13 cases; CK 6 in 11 cases; and CK 10 in five cases. In 13 cases of dysplasia, o nly simple epithelial antigens were identified. Involucrin expression was observed in 17 dysplastic biopsies and PNA in 12. By Fisher's exac t test, a significant association between non-severe histological grad e of dysplasia and CK 6 expression (P=0.018) was found. Comparison of the results using the same analysis showed significant correlations be tween the loss of CK 6 expression (P<0.001) and the expression of CK 1 4 (P=0.008) and involucrin (P=0.0018) with bronchial dysplasia. These data show that the pattern of differentiation antigen expression in br onchial dysplasia is significantly different from that of the normal b ronchial epithelium, but the phenotypic heterogeneity of these lesions is similar to that of bronchial carcinomas.