U. Diedrich et al., LOSS OF ALLELES IN BRAIN-TUMORS - DISTRIBUTION AND CORRELATIONS WITH CLINICAL COURSE, Journal of neurology, 242(10), 1995, pp. 707-711
Gliomas (n = 44) and meningiomas (n = 24) of different grades of malig
nancy were analysed for allele losses at loci on chromosomes 10, 13, 1
7 and 22. Deletions of genetic material on these chromosomes occurred
in gliomas without being restricted to any histological entity. The fr
equency of chromosome-10-specific allele losses increased significantl
y with the age of the patients and with the grade of malignancy of the
tumours. Deletions of chromosome 10 material were associated with a p
oor prognosis, The glioblastomas of patients aged over 70 years lacked
the loss of the entire chromosome 10, even in tumours with EGFR gene
amplification. Deletions at loci of chromosomes 13, 17 and 22 were obs
erved in 18-32% of all gliomas, independent of grade of malignancy, pa
tients' age, EGFR gene amplification and clinical course. Only chromos
ome-22-specific allele losses were found preferentially in gliomas of
female patients, Loss of chromosome 22 alleles in 44% was the only mut
ation detected in meningiomas. This occurred independently of grade of
malignancy and biological factors.