DNA copy number changes in high-grade malignant peripheral nerve sheath tumors by array CGH

• Published in: Molecular cancer Vol. 7; no. 1; p. 48
• Main Authors: Kresse, Stine H, Skårn, Magne, Ohnstad, Hege O, Namløs, Heidi M, Bjerkehagen, Bodil, Myklebost, Ola, Meza-Zepeda, Leonardo A
• Format: Journal Article
• Language: English
• Published: England BioMed Central Ltd 03-06-2008; BioMed Central; BMC
• Subjects: Adenovirus E1A Proteins - genetics; Adult; Aged; Amino Acid Oxidoreductases - genetics; Antigens, Neoplasm - genetics; Chromosomes, Human, Pair 17; Chromosomes, Human, Pair 8; DNA; DNA Topoisomerases, Type II - genetics; DNA, Neoplasm - analysis; DNA-Binding Proteins - genetics; Female; Gene Dosage; Gene Expression Profiling - methods; Gene Expression Regulation, Enzymologic; Gene Expression Regulation, Neoplastic; Genetic aspects; Humans; Inhibitor of Apoptosis Proteins; Male; Methods; Microtubule-Associated Proteins - genetics; Middle Aged; Neoplasm Proteins - genetics; Nerve Sheath Neoplasms - enzymology; Nerve Sheath Neoplasms - genetics; Nerve Sheath Neoplasms - mortality; Nervous system tumors; Nucleic acid hybridization; Oligonucleotide Array Sequence Analysis; Physiological aspects; Poly-ADP-Ribose Binding Proteins; Prognosis; Proto-Oncogene Proteins - genetics; Reverse Transcriptase Polymerase Chain Reaction; Risk factors; Soft Tissue Neoplasms - enzymology; Soft Tissue Neoplasms - genetics; Soft Tissue Neoplasms - mortality; Norway
• ISSN: 1476-4598; 1476-4598
• DOI: 10.1186/1476-4598-7-48

Malignant peripheral nerve sheath tumors (MPNSTs) are rare and highly aggressive soft tissue tumors showing complex chromosomal aberrations. In order to identify recurrent chromosomal regions of gain and loss, and thereby novel gene targets of potential importance for MPNST development and/or progression, we have analyzed DNA copy number changes in seven high-grade MPNSTs using microarray-based comparative genomic hybridization (array CGH).
Considerable more gains than losses were observed, and the most frequent minimal recurrent regions of gain included 1q24.1-q24.2, 1q24.3-q25.1, 8p23.1-p12, 9q34.11-q34.13 and 17q23.2-q25.3, all gained in five of seven samples. The 17q23.2-q25.3 region was gained in all five patients with poor outcome and not in the two patients with disease-free survival. cDNA microarray analysis and quantitative real-time reverse transcription PCR were used to investigate expression of genes located within these regions. The gene lysyl oxidase-like 2 (LOXL2) was identified as a candidate target for the 8p23.1-p12 gain. Within 17q, the genes topoisomerase II-alpha (TOP2A), ets variant gene 4 (E1A enhancer binding protein, E1AF) (ETV4) and baculoviral IAP repeat-containing 5 (survivin) (BIRC5) showed increased expression in all samples compared to two benign tumors. Increased expression of these genes has previously been associated with poor survival in other malignancies, and for TOP2A, in MPNSTs as well. In addition, we have analyzed the expression of five micro RNAs located within the 17q23.2-q25.3 region, but none of them showed high expression levels compared to the benign tumors.
Our study shows the potential of using DNA copy number changes obtained by array CGH to predict the prognosis of MPNST patients. Although no clear correlations between the expression level and patient outcome were observed, the genes TOP2A, ETV4 and BIRC5 are interesting candidate targets for the 17q gain associated with poor survival.