Application program 2011 open now

The Translational Research Training in Hematology (TRTH) award will give young researchers the tools, mentoring, and access...

 

EHA Jean Bernard Lifetime Achievement Award

Dr Emili Montserrat is be the third recipient of the Jean Bernard Lifetime Achievement Award which was presented for the fir...

 

EHA Fellowship Winners

The EHA Fellowship Winners of 2010 have received their award during the 15th Congress: Oxana Bereschenko, Florian Kuchenbaue...

 

EHA - José Carreras Award

The EHA - José Carreras Award is established to honour leading figures in hematological research and will be presented to an...

 

E H A / News / 11th Congress News / Acute myeloid leukemia

Simultaneous session on acute myeloid leukemia

Dr Bolli described the competition between NPM leukemic mutants and ARF protein.

He showed that mutant NPM protein binds less ARF protein than normal and this leads to ARF delocalization and degradation, thus promoting oncogenic events.

A novel FLT3-ITD627E mutation has been described by Dr Breitenbucher. This is a novel non JM-ITD that is resistant to PKC412, SU5614 and all the other tyrosine kinase inhibitors.

Dr Rucker showed that characterization of AML with complex karyotypes by microarrays allowed identification of recurrent genomic imbalances. Overexpression of new candidate genes such as ETS family genes was detected.

138 cases of NPM1-mutated/FLT3 ITD negative AML with normal karyotype were screened by gene expression profiling. Dr Bullinger described a distinct gene expression pattern : the amplification of some genes like APP and deregulation of the Notch signaling pathway.

Dr van der Holt told us that MDR1 single nucleotide polymorphisms did not influence MDR function andPgp expression. There is no impact on clinical outcome and SNPs do not exert a major impact on drug resistance in patients with AML.

Last updated on Saturday 17 June 2006.