Acta Neuropathologica

, Volume 81, Issue 6, pp 675–679

Proliferating cell nuclear antigen and Ki-67 immunohistochemistry in brain tumors: A comparative study

Authors

  • D. N. Louis
    • Department of Pathology (Neuropathology)Massachusetts General Hospital
  • S. Edgerton
    • Department of Pathology (Neuropathology)Massachusetts General Hospital
  • A. D. Thor
    • Department of Pathology (Neuropathology)Massachusetts General Hospital
  • E. T. Hedley-Whyte
    • Department of Pathology (Neuropathology)Massachusetts General Hospital
Regular Papers

DOI: 10.1007/BF00296379

Cite this article as:
Louis, D.N., Edgerton, S., Thor, A.D. et al. Acta Neuropathol (1991) 81: 675. doi:10.1007/BF00296379

Summary

Proliferating cell nuclear antigen (PCNA) is a 36-kDa DNA polymerase-σ auxiliary protein which accumulates in the nucleus during S phase of the cell cycle. Immunohistochemical labeling indices (LI) of PCNA and Ki-67 were compared using an avidin-biotin complex method on frozen sections of 27 nervous system tumors, 3 normal cerebral cortices, and 3 peripheral nerves. In glial tumors, PCNA and Ki-67 LI increased with increasing tumor grade (Daumas-Duport system). In 5 low-grade glial tumors, PCNA and Ki-67 LI were ≤1%, except for one optic nerve glioma (Ki-67 LI=6%). In 7 grade 3 astrocytomas, and 1 mixed glioma, PCNA LI were ≤1–1.5%, while Ki-67 LI were 2%–10%. In 7 grade 4 astrocytomas and 1 metastatic carcinoma, PCNA LI ranged from 6%–15% while Ki-67 LI ranged from 17%–30%. In 5 of 6 schwannomas, focally high PCNA LI (4%–65%) were noted, despite low LI with Ki-67 (≤1.6%). Scattered normal schwann cell nuclei also stained with PCNA, but normal cerebral cortex did not. These data suggest that: (1) in higher-grade gliomas, PCNA may be a more specific S-phase marker, although a less sensitive proliferation marker, than Ki-67; (2) PCNA LI do not distinguish low-grade gliomas from grade 3 astrocytomas; (3) in schwannomas, PCNA may not reflect proliferative activity since it seems to react with an epitope present in normal schwann cells; and (4) the variable PCNA staining pattern introduces greater difficulties in cell counting than with Ki-67. These factors may limit the use of this anti-PCNA antibody in evaluating nervous system tumors.

Key words

Proliferating cell nuclear antigen (PCNA) Ki-67 Immunohistochemistry Nervous system tumors

Copyright information

© Springer-Verlag 1991