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12th Congress of the European Hematology ... - Haematologica

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derivative chromosome (4p16, 7p14, 13q14, and 11q13, respectively);<br />

among <strong>the</strong>m, only in one case <strong>the</strong> loss <strong>of</strong> miRNAs on <strong>the</strong> third derivative<br />

was not associated with <strong>the</strong> miRNAs deletion mapped on chromosome<br />

9. The most recurrent miRNAs deleted on der(9) were mir-219-2<br />

(deleted in 100% <strong>of</strong> cases) and mir-199-b (lost in 67% <strong>of</strong> cases). It is<br />

noteworthy that mir-219-2 neighbors and overlaps CpG-islands, suggesting<br />

a potential role <strong>of</strong> this miRNA in CpG-island methylation. Conclusions.<br />

Experimental studies indicate that miRNAs can function as<br />

tumor suppressor genes or as oncogenes. In fact, in chronic lymphocytic<br />

leukemia associated with del(13)(q14) it has been demonstrated that<br />

<strong>the</strong> miRNAs loss can induce downregulation <strong>of</strong> <strong>the</strong> antiapoptotic BCL-<br />

2 protein. The novel evidence that deletions on der(9) in CML are associated<br />

with miRNAs loss may shed new light on <strong>the</strong> significance <strong>of</strong><br />

genomic sequences loss. Fur<strong>the</strong>r studies are needed since it is known that<br />

some microRNAs may have as many as a few thousand targets, so prediction<br />

algorithms and strategies allowing large-scale screening <strong>of</strong> multiple<br />

target genes are required.<br />

0540<br />

SEMEN ANALYSIS DURING IMATINIB THERAPY IN PATIENTS WITH CHRONIC MYELOID<br />

LEUKEMIA<br />

F. Maloisel, 1 A. Zamfir, 2 K Bennada, 2 A. Clavert3 1 Hôpitaux Universitaires, STRASBOURG; 2 Department <strong>of</strong> <strong>Hematology</strong> &<br />

Oncology, STRASBOURG; 3 CECOS, STRASBOURG, France<br />

Background. Imatinib is <strong>the</strong> main treatment <strong>of</strong> chronic myeloid<br />

leukaemia and induces high rate <strong>of</strong> cytogenetic response and major<br />

molecular response. The 5 years survival from IRIS trial is 87% and <strong>the</strong><br />

annual risk <strong>of</strong> relapse for responder patients is about 1% by year. Imatinib<br />

is a strong inhibitor <strong>of</strong> bcr-abl, c-kit and PDGF-R, and could explain<br />

sides effects related to <strong>the</strong> drug. C-kit is involved during spermatogenesis<br />

and influenced <strong>the</strong> spermatogonies maturation. Imatinib induces<br />

qualitative and quantitative deteriorations <strong>of</strong> spermograms in rats. Data<br />

about qualitative and quantitative characteristics <strong>of</strong> spermograms from<br />

patients treated with imatinib are lacking and sperm cryopreservation<br />

before treatment is recommanded. Methods. Semen cryopreservation<br />

was performed at diagnosis before treatment to every patient under 50<br />

years <strong>of</strong> age. After information and fully consenting, patients aged >17<br />

and

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