Genome profiles of familial/bilateral and sporadic testicular germ cell tumors

• Published in: Genes chromosomes & cancer 2002-06, Vol.34 (2), p.168-174
• Main Authors: Kraggerud, Sigrid Marie, Skotheim, Rolf I., Szymanska, Jadwiga, Eknæs, Mette, Fosså, Sophie D., Stenwig, Anna E., Peltomäki, Päivi, Lothe, Ragnhild A.
• Format: Article
• Language: English
• Subjects: Adult; Chromosome Deletion; Gene Amplification - genetics; Gene Dosage; Genes, Overlapping - genetics; Genome, Human; Genomics - methods; Germinoma - genetics; Humans; Male; Nucleic Acid Hybridization; Seminoma - genetics; Testicular Neoplasms - genetics
• ISSN: 1045-2257; 1098-2264
• DOI: 10.1002/gcc.10058

In order to investigate the genetics of testicular germ cell tumors (TGCTs), we examined 33 TGCTs, including 15 familial/bilateral and 18 sporadic tumors, using comparative genomic hybridization. The frequencies of the histological subtypes were comparable between the two groups. Gains of the whole or parts of chromosome 12 were found in 30 tumors (91%). Furthermore, increased copy number of the whole or parts of chromosomes 7, 8, 17, and X, and decreased copy number of the whole or parts of chromosomes 4, 11, 13, and 18 were observed in ≥50% of the tumors. Sixteen smallest regions of overlapping changes were delineated on 12 different chromosomes. The chromosomal copy numbers of familial/bilateral and sporadic TGCTs were comparable, suggesting similar genetic pathways to disease in both groups. However, significant differences were observed between the two main histological subgroups. Gains from 15q and 22q were associated with seminomas (P = 0.005 and P = 0.02, respectively), whereas gain of the proximal 17q (17q11.2–21) and high‐level amplification from chromosome arm 12p, and losses from 10q were associated with nonseminomas (P < 0.001, P = 0.04, and P = 0.03, respectively). © 2002 Wiley‐Liss, Inc.