BioDiscovery (Oct 2012)

Does positioning of chromosomes 8 and 21 in interphase drive t(8;21) in acute myelogenous leukemia?

  • Moneeb A.K. Othman,
  • Amelie Lier,
  • Susann Junker,
  • Philipp Kempf,
  • Franziska Dorka,
  • Erich Gebhart,
  • Frenny J. Sheth,
  • Beata Grygalewicz,
  • Samarth Bhatt,
  • Anja Weise,
  • Kristin Mrasek,
  • Thomas Liehr,
  • Marina Manvelyan

DOI
https://doi.org/10.7750/BioDiscovery.2012.4.2
Journal volume & issue
Vol. 4
pp. 1 – 5

Abstract

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The impact of chromosome architecture in the formation of chromosome aberrations is a recent finding of interphase directed molecular cytogenetic studies. There evidence was provided that disease specific chromosomal translocations could be due to tissue specific genomic organization. In a recent small pilot study using three-dimensional interphase fluorescence in situ hybridization, we showed that there might be a specific chromosome positioning in myeloid bone marrow cells, i.e. a co-localization of chromosomes 8 and 21. Here we could substantiate this finding in overall 21 studied cases with acute myeloid leukemia (AML) that there is even a co-localization of the genes AML1 and ETO. This finding led to the suggestion that a specific interphase architecture of myeloid bone marrow cells might promote the typical t(8;21)(q22;q22) leading to AML-M2.

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