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Journal of Neurology, Neurosurgery, and Psychiatry 2003;74:779-783; doi:10.1136/jnnp.74.6.779
Copyright © 2003 by the BMJ Publishing Group Ltd.
Journal of Neurology Neurosurgery and Psychiatry 2003;74:779-783
© 2003 BMJ Publishing Group

PAPER

p53, mdm2, EGFR, and msh2 expression in paired initial and recurrent glioblastoma multiforme

A M Stark, P Witzel, R J Strege, H-H Hugo and H M Mehdorn

Department of Neurosurgery, University of Kiel Medical Centre, Kiel, Germany

Correspondence to:
Correspondence to:
Dr Andreas M Stark, Department of Neurosurgery, University of Kiel Medical Centre, Weimarer Str 8, D-24106 Kiel, Germany;
andstark{at}hotmail.com

Background: The clinical course of glioblastoma multiforme is characterised by invasive growth and regular recurrence. Many genetic alteration have been identified in the genesis of the disease. However, information about immunohistochemical expression in recurrent lesions is sparse.

Objectives: To determine (1) whether the p53/mdm2/EGFR/msh2 expression pattern differs in initial v recurrent glioblastoma multiforme; (2) whether a possible change in expression correlates with prognostic variables (progression-free survival time, total survival time); and (3) whether chemotherapy in addition to surgery and radiotherapy influences the p53/mdm2/EGFR/msh2 expression profile.

Methods: 27 patients were studied. They met the following criteria: histologically confirmed diagnosis of glioblastoma multiforme (WHO IV); total tumour resection at initial craniotomy; at least one re-craniotomy for glioblastoma multiforme recurrence; age 21 years or older. All underwent radiotherapy of at least 54 Gy, and 17 received additional chemotherapy. Immunohistochemical staining of initial tumours and recurrences was done with the following monoclonal antibodies: anti-p53 (DO-1), anti-mdm2 (IF-2), anti-EGFR (H11), and anti-msh2 (AB-1).

Results: In comparison with the initial tumour, recurrent lesions were characterised by reduced expression of p53 (p < 0.0001) and msh2 (p = 0.0012), while the numbers of mdm2 (p = 0.02), EGFR (p < 0.0001), and msh2 positive specimens (p < 0.0001) were reduced. Chemotherapy was associated with reduced msh2 expression (p < 0.0001). Immunohistochemical variables were not associated with patient survival.

Conclusions: There are significant differences in the p53/mdm2/EGFR/msh2 expression patterns in initial v recurrent glioblastoma multiforme. There may be interactions between chemotherapy and changes in the msh2 expression.

Keywords: EGFR; glioblastoma; msh2; p53


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This article has been cited by other articles:

  • (2003). Immunohistochemical expression patterns differ in recurrent and initial glioblastoma multiforme. J. Clin. Pathol. 56: 865-865 [Full Text]  

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