PROLIFERATIVE ACTIVITY IN SPITZ NEVI COMPARED WITH OTHER MELANOCYTIC SKIN-LESIONS

被引:7
作者
HOFMANNWELLENHOF, R
RIEGER, E
SMOLLE, J
KERL, H
机构
[1] Department of Dermatology, University of Graz Auenbruggerplatz
关键词
IMAGE ANALYSIS; PCNA; SPITZ NEVI;
D O I
10.1097/00008390-199310000-00002
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Proliferative activity has been shown to correlate with the degree of malignancy in various human neoplasms Immunostaining with the monoclonal antibody PC10 binding to proliferating cell nuclear antigen (PCNA) facilitates the assessment of proliferation in routinely fixed, paraffin-embedded tissue sections. In this study we investigated the expression of PCNA in 29 Spitz's naevi In comparison with 43 primary malignant melanomas (MM), 18 cutaneous metastases of malignant melanoma (MMM) and 16 benign melanocytic naevl (BMN). After selection al the microscopic field with the highest number of PCNA-positive nuclei, the nuclear density (ND(max)) of PCNA-stained nuclei in this field was assessed using interactive image analysis. The mean value of ND(max) (given as 1000 nuclei/mm3 tissue) of SN was 27.9 (+/-16.7) and differed significantly from that of MM (48.1 +/- 40.5; U-test: p<0.05) and that of MMM (114.4 +/- 56.3; p<0.01). Comparing ND(max) of the subgroups of MM according to their maximal vertical tumour thickness with ND(max) of SN we found significant differences only between SN and MM > 1.5 mm thick (n = 14; ND(max) = 67.8 +/- 36.1) but not between SN and MM less-than-or-equal-to 1.5 mm thick (n = 29; ND(max) = 38.8 +/- 39.3). PCNA expression in SN did not differ from that of BMN (ND(max) 23.8 +/- 28.5). Proliferative activity as assessed by measurement of PCNA expression therefore showed significant differences between BMN, SN and thin primary melanomas on one hand and thick primary melanomas and cutaneous metastases of malignant melanomas on the other hand.
引用
收藏
页码:313 / 317
页数:5
相关论文
共 35 条
[11]  
Takahashi H., Strutton G.M., Parson P.G., Determination of proliferating fraction in malignant melanomas by anti-PCNA/cyclin monoclonal antibody, Histopathology, 18, pp. 221-227, (1991)
[12]  
Ackerman A.B., Niven J., Grant-Kels J.M., Differential Diagnosis in Dermatopathology, Lea and Febiger, Philadelphia, (1982)
[13]  
Hofmann-Wellenhof R., Smolle J., Kerl H., The influence of staining procedures on the assessment of cell proliferation as defined by monoclonal antibody Ki-67, Am J Dermatopathol, 12, pp. 458-461, (1990)
[14]  
Weibel E.R., Stereological methods, 1, (1979)
[15]  
Weibel E.R., Stereological methods, 2, (1980)
[16]  
Stone C.H., Ma C.K., Lynch E.J., Expression of proliferating cell nuclear antigen (PCNA) in adult Spitz nevi: Comparison with deep malignant melanoma, Mod Pathol, 36 A, (1993)
[17]  
Hall P.A., Levison D.A., Woods A.L., Proliferating cell nuclear antigen (PCNA) immunolocalization in paraffin sections: An index of cell proliferation with evidence of deregulated expression in some neoplasms, J Pathol, 162, pp. 285-294, (1990)
[18]  
Kamel O.W., Lebrun D.P., Davis R.E., Growth fraction estimation of malignant lymphomas in formalin-fixed paraffin-embedded tissue using anti-PCNA/cyclin 19A2. Correlation with Ki-67 labelling, Am J Pathol, 138, pp. 1471-1477, (1991)
[19]  
Van Dierendonck J.H., Wisjman J.H., Keizer R., Cell-cycle-related staining patterns of anti-proliferating cell nuclear antigen monoclonal antibodies. Comparison with BrdUrd labeling and Ki-67 staining, Am J Pathol, 138, pp. 1165-1172, (1991)
[20]  
Miyagawa S., Okada N., Takahashi Y., Expression of proliferating cell nuclear antigen/cyclin in human keratin-ocytes, J Invest Dermatol, 93, pp. 678-681, (1989)