Spatial variability of genomic aberrations in a large glioblastoma resection specimen

• Published in: Acta neuropathologica Vol. 102; no. 1; pp. 103 - 109
• Main Authors: KROS, Johan M, VAN RUN, Peter R. W. A, ALERS, Janneke C, AVEZAAT, Cees J. J, LUIDER, Theo M, VAN DEKKEN, Herman
• Format: Journal Article
• Language: English
• Published: Berlin Springer 01-07-2001; Springer Nature B.V
• Subjects: Biological and medical sciences; Brain cancer; Brain Neoplasms - diagnosis; Brain Neoplasms - genetics; Brain Neoplasms - pathology; Chromosome 9; Chromosome aberrations; Genetic Variation; Genome; Genomic instability; Genotype; Glioblastoma; Glioblastoma - diagnosis; Glioblastoma - genetics; Glioblastoma - pathology; Glioma; Humans; Hybridization; Magnetic Resonance Imaging; Male; Medical sciences; Metastases; Middle Aged; Neurology; Nucleic Acid Hybridization; Sampling error; Tumors of the nervous system. Phacomatoses; Case study; Human; Malignant glioma; Nervous system diseases; Comparative genomic hybridization; Pathophysiology; Central nervous system disease; Glioblastoma; Malignant tumor
• ISSN: 0001-6322; 1432-0533
• DOI: 10.1007/s004010000327

In the present study, the distribution of genetic aberrations in a glioblastoma resection specimen of unusually large size (9x8x2 cm) was investigated using comparative genomic hybridization (CGH). CGH was performed on 20 samples taken from the specimen, and the genetic aberrations found were compared with the regional histology. The samples were histopathologically graded according to WHO criteria, and a division in high- and low-grade areas and infiltration rims was made. In high-grade areas, low-grade areas as well as infiltration rims, gains on 10p11.2-pter (14/20), 11q12-q22 (6/20) and losses on 4q13-qter (9/20), 10q22-qter (8/20), 11p14-pter (5/20), 13q12-qter (7/20) were revealed. Gains on 1q21-32 (2/4) and losses on 7p21-pter (3/4) were exclusively found in the high-grade areas. In the low-grade tumor samples and in the infiltration rim, gains on 16p11.2-pter (6/16), 17p11.2-pter (6/16), 17q11.2-qter (5/16), 20q11.2-q13 (3/16) and deletions on 5q31-qter (4/16) were detected. Gains on 7q21-qter (8/11) and 8q11.2-qter (6/11), and loss of chromosome 9 (4/11) and the Y-chromosome (4/11) were found in the high-grade and low-grade samples, not in the infiltration rims. The finding of a set of identical chromosomal aberrations throughout the resection specimen, most of which have been previously reported in gliomas, confirms a mechanism of clonal tumor proliferation operative in gliomas. The previously unreported genetic alterations which were predominantly traced in the tumor rims, might reflect either selection for properties related to infiltrating behavior, or genomic instability of subclones. The findings illustrate the importance of searching for high-grade genetic aberrations in low-grade tumor samples taken from cases in which sampling error is suspected.