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SHR Neuro Cancer Cardio Lipid Metab Microb

Schick, B; Wemmert, S; Bechtel, U; Nicolai, P; Hofmann, T; Golabek, W; Urbschat, S.
Comprehensive genomic analysis identifies MDM2 and AURKA as novel amplified genes in juvenile angiofibromas.
Head Neck. 2007; 29(5):479-487 Doi: 10.1002/hed.20535
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Co-authors Med Uni Graz
Hofmann Thiemo
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Abstract:
BACKGROUND: Frequent beta-catenin mutations have been detected in juvenile angiofibromas, but the tumor pathogenesis remains unknown. METHODS: Metaphase-comparative genomic hybridization (CGH) was used to identify chromosomal aberrations in 29 tumor specimens. Two tumors were investigated using genome DNA microarrays. RESULTS: Three hundred eleven chromosomal gains and losses were detected by metaphase-CGH. Frequent chromosomal gains were detected at 4q, 6, 12, and X, while frequent chromosomal losses affected regions of chromosomes 8, 16, 17, 22, and Y. Genome DNA microarray analysis in 2 tumors of the series confirmed chromosomal aberrations, detected by metaphase-CGH, and indicated genes such as AURKA (20q13.2) not being recognized by metaphase-CGH. CONCLUSION: Metaphase-CGH results confirmed numerous chromosomal aberrations in juvenile angiofibromas. The most frequent aberrations affected sex chromosomes. Further consensus regions of chromosomal aberrations were detected at 4q, 6, 8, 12, 16, 17, and 22. AURKA and MDM2 were identified as interesting novel amplified genes in juvenile angiofibromas.
Find related publications in this database (using NLM MeSH Indexing)
Angiofibroma - genetics
Chromosome Aberrations - genetics
Head and Neck Neoplasms - genetics
Humans - genetics
Male - genetics
Metaphase - genetics
Nucleic Acid Hybridization - methods
Oligonucleotide Array Sequence Analysis - methods
Protein-Serine-Threonine Kinases - genetics
Proto-Oncogene Proteins c-mdm2 - genetics

Find related publications in this database (Keywords)
juvenile angiofibroma
genetics
CGH
microarray
genomic instability
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