An immunohistochemical study of keratin expression in ameloblastoma from a Kenyan population

被引:0
作者
Ong'uti, MN [1 ]
Howells, GL [1 ]
Williams, DM [1 ]
机构
[1] St Bartholomews & Royal London Sch Med & Dent, Oral Dis Res Ctr, London E1 2AD, England
关键词
ameloblastoma; differentiation; immunohistochemistry; keratin proliferation;
D O I
暂无
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
OBJECTIVES: Ameloblastomas appear to exhibit biological heterogeneity and, except in the case of malignancy, histological appearances that do not always allow their behaviour to be predicted. The aim of this study was to assess keratin expression in African ameloblastomas and to correlate this with their clinical and histological features. MATERIALS AND METHODS: Expression of simple keratins 7, 8, 18 and 19; cornification keratins 1 and 10; basal and differentiation keratins 5 and 14 and hyperproliferation-related keratins 6 and 16 in 14-39 cases of ameloblastoma was assessed by immunohistochemical methods. RESULTS: There was patchy expression of keratin 7 in the suprabasal and stellate reticulum-like cells in some cases. All cases showed similar weak expression for keratins 8 and 18 in suprabasal and stellate reticulum-like cells but none showed keratin 1 or 10 expression, There was intense expression of keratins 5, 14 and 19 by all tumour cells suggesting that they may retain basal cell characteristics with a potential for proliferation. No consistent relationship was seen between histological types and keratin expression pattern. However, keratins 6 and 16, expressed by suprabasal and stellate reticulum-like cells, showed a marked variation within and between cases, with the highest levels of expression in squamous strands. CONCLUSIONS: We propose that squamous strands may represent the sites of most active growth within individual tumours and expression of keratins 6, 16 and 19 may be predictors of rapid growth. There is a need for further investigation of this in longitudinal clinical studies.
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页码:111 / 116
页数:6
相关论文
共 25 条
[1]  
ADEMOLA AO, 1993, J CRANIOMAXILLOFAC S, V21, P351
[2]   PATTERNS OF EXPRESSION OF INTERMEDIATE FILAMENTS IN AMELOBLASTOMA AND HUMAN-FETAL TOOTH GERM [J].
HEIKINHEIMO, K ;
HORMIA, M ;
STENMAN, G ;
VIRTANEN, I ;
HAPPONEN, RP .
JOURNAL OF ORAL PATHOLOGY & MEDICINE, 1989, 18 (05) :264-273
[3]  
HEIKINHEIMO K, 1991, LAB INVEST, V65, P688
[4]   DISTRIBUTION OF INTERMEDIATE-FILAMENT PROTEINS IN THE HUMAN-ENAMEL ORGAN - UNUSUALLY COMPLEX PATTERN OF COEXPRESSION OF CYTOKERATIN POLYPEPTIDES AND VIMENTIN [J].
KASPER, M ;
KARSTEN, U ;
STOSIEK, P ;
MOLL, R .
DIFFERENTIATION, 1989, 40 (03) :207-214
[5]   MONOCLONAL-ANTIBODIES PROVIDE SPECIFIC INTRAMOLECULAR MARKERS FOR THE STUDY OF EPITHELIAL TONOFILAMENT ORGANIZATION [J].
LANE, EB .
JOURNAL OF CELL BIOLOGY, 1982, 92 (03) :665-673
[6]   KERATIN ANTIGENS IN DIFFERENTIATING SKIN [J].
LANE, EB ;
BARTEK, J ;
PURKIS, PE ;
LEIGH, IM .
ANNALS OF THE NEW YORK ACADEMY OF SCIENCES, 1985, 455 :241-258
[7]  
LANE EB, 1990, CANCER BIOL, V1, P165
[8]  
LINDBERG K, 1989, AM J PATHOL, V134, P89
[9]   INSITU HYBRIDIZATION ANALYSIS OF KERATIN GENE-EXPRESSION IN HUMAN AMELOBLASTOMAS [J].
LUO, W ;
ROOP, DR ;
LAU, EC ;
MELROSE, RJ ;
MOSTOFI, R ;
STENMAN, G ;
SNEAD, ML .
JOURNAL OF ORAL PATHOLOGY & MEDICINE, 1988, 17 (9-10) :534-540
[10]   KERATIN EXPRESSION IN BASAL-CELL CARCINOMAS [J].
MARKEY, AC ;
LANE, EB ;
MACDONALD, DM ;
LEIGH, IM .
BRITISH JOURNAL OF DERMATOLOGY, 1992, 126 (02) :154-160