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Analysis of chromosomal imbalances in sporadic and NF1‐associated peripheral nerve sheath tumors by comparative genomic hybridization
Author(s) -
Mechtersheimer Gunhild,
OtañoJoos Marta,
Ohl Sibylle,
Benner Axel,
Lehnert Thomas,
Willeke Frank,
Möller Peter,
Otto Herwart F.,
Lichter Peter,
Joos Stefan
Publication year - 1999
Publication title -
genes, chromosomes and cancer
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.754
H-Index - 119
eISSN - 1098-2264
pISSN - 1045-2257
DOI - 10.1002/(sici)1098-2264(199908)25:4<362::aid-gcc8>3.0.co;2-q
Subject(s) - comparative genomic hybridization , neurofibromatosis , biology , chromosome , malignant peripheral nerve sheath tumor , cancer research , chromosomal deletion , chromosomal region , pathology , cancer , carcinogenesis , tumor suppressor gene , gene , genetics , medicine
Peripheral nerve sheath tumors arise either sporadically or in association with neurofibromatosis type 1 (von Recklinghausen's neurofibromatosis, NF1) or type 2. In this study, comprehensive screening for relative chromosome copy number changes was performed on 10 benign and 19 malignant peripheral nerve sheath tumors (MPNSTs) by applying comparative genomic hybridization (CGH). In benign tumors, no chromosomal imbalances were found by CGH, whereas in MPNSTs chromosomal gains and losses were frequently detected. No differences regarding the frequency and distribution of chromosomal imbalances were observed between the 13 sporadic and 6 NF1‐associated MPNSTs analyzed. In both, the number of gains was significantly higher than the number of losses, suggesting a predominant role of proto‐oncogene activation during MPNST progression. Candidate regions with potentially relevant proto‐oncogenes included chromosomal bands 17q24–q25, 7p11–p13, 5p15, 8q22–q24, and 12q21–q24; those with putative tumor suppressor genes were 9p21–p24, 13q14–q22, and 1p. High‐level amplifications were restricted to sporadic tumors and affected eight different chromosomal subregions. In three of these MPNSTs, identical subregions on chromosomal arms 5p and 12q were coamplified. This study revealed a number of new characteristic chromosomal imbalances and provides a basis for molecular identification of oncogenes and tumor suppressor genes of pathogenetic relevance in both sporadic and NF1‐associated MPNSTs. Genes Chromosomes Cancer 25:362–369, 1999. © 1999 Wiley‐Liss, Inc.