COMPARISON OF IMMUNOSTAININGS FOR PROLIFERATING CELL NUCLEAR ANTIGEN AND KI-67 IN HUMAN EXTRAOCULAR LESIONS
Citation
T. Kodama et al., COMPARISON OF IMMUNOSTAININGS FOR PROLIFERATING CELL NUCLEAR ANTIGEN AND KI-67 IN HUMAN EXTRAOCULAR LESIONS, Graefe's archive for clinical and experimental ophthalmology, 235(12), 1997, pp. 767-772
Categorie Soggetti
Ophthalmology
SICI code
0721-832X(1997)235:12<767:COIFPC>2.0.ZU;2-E
Abstract
Background: Cell kinetic information is helpful to understand disease
progression, treatment response, and prognosis of the neoplasms. To co
mpare the usefulness and limitations of antibodies that recognize the
cell cycle-associated molecules, proliferating cell nuclear antigen (P
CNA) and Ki-67, we performed immunostaining in formalin-fixed, paraffi
n-embedded tissue sections of extraocular lesions. Methods: Specimens
were obtained from patients undergoing routine surgical procedures. Fo
rmalin-fixed, paraffin-embedded sections were stained for PCNA and Ki-
67 using the monoclonal antibodies PC10 and MIB-1, respectively. Micro
wave oven heating for antigen retrieval was performed before immunosta
ining. Results: In squamous cell carcinomas and basal cell carcinomas,
PCNA immunostaining varied greatly. Basal cells of benign epithelial
lesions showed moderate to weak PCNA staining. Strong PCNA immunoreact
ivity was demonstrated in foci of inflammation and germinal centers. M
icrowave processing en hanced the intensity of those PCNA immunostaini
ngs. As the PCNA immunostaining intensity had a great variability, the
absolute numbers of PCNA-positive cells were hard to count in some ti
ssues. High Ki-67 counts were observed in squamous cell carcinomas, fo
ci of inflammatory cells, and germinal center cells. Basal cell carcin
omas and benign lesions showed low Ki-67 counts. Every section showed
clear nuclear staining in Ki-67 immunostaining. Conclusion: Careful co
nsideration is required in the assessment of cell proliferation using
PCNA. The immunostaining of Ki-67 may be more accurate than that of PC
NA for evaluating cell proliferation in formalin-fixed, paraffin-embed
ded tissues.