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Authors (total 1517) bold: presenting authors Abraham Kaipparettu ...

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Anke Ehlers, Michael Hummel, Harald Stein<br />

Epigenetic Transdifferentiation in Hodgkin Lymphoma<br />

A special feature of the B-cell derived Hodgkin and Reed-Sternberg cells in classic<br />

Hodgkin lymphoma is the constant lack of expression of most B-cell characteristic<br />

markers. Several mechanisms leading to this markedly different phenotype (e.g.<br />

mutations or lack of transcription factors etc.) have been discussed, but so far the<br />

fundamental switch in the transcriptional program remains a mystery. In recent years it<br />

has become apparent that transcriptional silencing can also be associated with<br />

epigenetic changes. To study the role of epigenetic DNA and/or histone alterations in<br />

Hodgkin lymphoma, we treated Hodgkin and Non-Hodgkin lymphoma cell lines with the<br />

demethylating agent 5’Aza-deoxy-cytidine and the Histone Deacetylase Inhibitor<br />

Trichostatin A. Subsequently we analysed the gene expression pattern of treated and<br />

untreated cell lines with gene expression oligonucleotide microarrays. The identification<br />

of distinct DNA methylation, histone acetylation and gene expression signatures provides<br />

novel insights into the molecular basis of tumor formation and understanding of the<br />

pathogenesis of Hodgkin lymphoma, which will be useful for tumor classification, as well<br />

as prediction of response to therapy and prognosis.<br />

contact:<br />

Dr. Anke Ehlers<br />

Charité Campus Benjamin Franklin<br />

Pathologie<br />

anke.ehlers@charite.de<br />

Hindenburgdamm 30<br />

12200 Berlin (Germany)

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