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Centrosome amplification is correlated with ploidy divergence, but not with MYCN amplification, in neuroblastoma tumors
Cancer Genetics and Cytogenetics, 12/31/08
Fukushi D et al. – Findings suggest that different mechanisms may generate centrosome amplification in cells of infant vs childhood diploid tumors; MYCN amplification was not correlated with centrosome amplification in sporadic neuroblastomas.
Methods- Study of whether centrosome amplification is correlated with ploidy status or MYCN amplification
- Immunostain of centrosomes
- Fluorescence in situ hybridization for ploidy and MYCN copy numbers in 27 neuroblastomas
- Tumors: 8 infant triploid, 9 infant diploid, 10 childhood diploid
- Ploidy divergence defined as mixed cell population with trisomy 1, with tetrasomy 1, and/or with pentasomy 1 in diploid tumors, and with tetrasomy 1 and pentasomy 1 in triploid tumors, each >5% of cells
- Ploidy divergence in 78% of infant diploid tumors, but not in triploid and childhood diploid tumors
- Higher incidences of centrosome amplification in childhood and infant diploid tumors than infant triploid tumors
- Only infant diploid tumors showed ploidy divergence, implying cytokinesis failure
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