Distinct molecular signatures in pediatric infratentorial glioblastomas defined by aCGH

• Published in: Experimental and molecular pathology 2010-10, Vol.89 (2), p.169-174
• Main Authors: Sharma, S., Free, A., Mei, Y., Peiper, S.C., Wang, Z., Cowell, J.K.
• Format: Article
• Language: English
• Subjects: Adolescent; Biological and medical sciences; CGH; Child; Chromosome Aberrations; Chromosomes, Human, Pair 17; Chromosomes, Human, Pair 7; Chromosomes, Human, Pair 8; Comparative Genomic Hybridization; DNA copy number; DNA Copy Number Variations; Female; Glioblastoma; Glioblastoma - genetics; Glioblastoma - pathology; Glioma; Humans; Infratentorial Neoplasms - genetics; Infratentorial Neoplasms - pathology; Investigative techniques, diagnostic techniques (general aspects); Male; Medical sciences; Molecular signature; Neurology; Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques; Pediatric glioma; Tumors of the nervous system. Phacomatoses
• ISSN: 0014-4800; 1096-0945
• DOI: 10.1016/j.yexmp.2010.06.009

Glioblastomas (GBM) are rare in children, but reportedly have more varied outcome which suggests differences in tumor etiology compared to typical GBM of adults. To investigate this we performed high resolution array comparative genomic hybridization (aCGH) analysis on three pediatric infratentorial GBM, ages 3.5, 7 and 14 years. Two of these tumors occurred in the brainstem and one in the spinal cord. While histologically typical, one brainstem tumor showed mainly pleomorphic astrocytic cells, whereas the other brainstem and spinal tumors showed a GFAP positive small cell component. Whole chromosomal gains (#1 and #2) and loss (#20) were seen only in the pleomorphic brainstem GBM, which also showed a high level of segmental genomic copy number changes. Segmental loss involving chromosome 8 was seen in all three tumors (Chr8;133039446-136869494, Chr8;pter-3581577, and Chr8;pter-30480019 respectively), whereas loss involving chromosome 16 was seen in only 2 cases with small cell components (Chr16;31827239-qter and Chr16;pter-29754532). Segmental gain of chromosome 7 was shared only between the 2 brainstem cases (Chr7;17187166-qter and Chr7;69824947-qter). Chromosome 17 showed segmental gain of 17q in the backdrop of loss of 17p only in case 1. Segmental gain of chromosome 1q was seen only in case 2. The spinal GBM showed a relatively stable karyotype with a unique loss of Chr19;32848902-qter. None of the frequent losses, gains and amplifications known to occur in adult GBM were identified, suggesting that pediatric infratentorial glioblastomas show a molecular karyotype that was more characteristic of pediatric embryonal tumors than adult GBM.