Publication Date:
2009-11-20
Description:
Abstract 2390 Poster Board II-367 In recent years miRNA expression patterns have been related to tumor (sub)type and disease outcome in various types of cancer, including acute myeloid leukemia (AML). Therefore, miRNA profiling may provide information for better classification and risk stratification of AML subtypes, and in addition may shed light on the underlying disease biology. To date large scale miRNA profiling has only been performed in adult AML, which differs from childhood AML in many ways, reflected in differences in cytogenetic subgroups, response to therapy and prognosis. However, knowledge on the role of miRNAs in childhood AML is limited. To answer the question if differential expression of miRNAs can be observed in subtypes of pediatric AML, we used quantitative RT-PCR to determine the expression levels of miR-29a, -155, -196a and -196b in a selection of de novo pediatric AML patients (n=49-84) representing the different cytogenetic subtypes. These miRNAs have been reported to be differentially expressed in cytogenetic and morphological subtypes of adult AML. In AML with t(10;11) MLL-rearrangements (n=5) versus all other AML samples expression of miR-29a was 2.4-fold lower (p=0.005). However, differences in expression of miR-29a in all MLL-rearranged AML compared to other AML patients were small and not significant, in contrast to what was found in adults. MiR-155 was upregulated 2.3-fold (p=0.0003) in FLT3-ITD-mutated AML (n=8) compared to all other AML samples, which is consistent to what has been reported for adult AML. The expression of both miRNA-196a and –196b differed extremely between patients. High expression of both miRNAs was observed in patients carrying MLL-gene rearrangements, NPM1 mutations, or FLT3-ITD mutations in a normal karyotype background. Low expression was found in t(8;21), inv(16) and t(15;17) subtypes (including those with FLT3-ITD mutations), and in patients with mutated CEBPA. The median difference between these groups of patients was 147-fold for miR-196a (n=73, p
Print ISSN:
0006-4971
Electronic ISSN:
1528-0020
Topics:
Biology
,
Medicine
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