MicroRNA-106b~25 cluster is upregulated in relapsed MLL-rearranged pediatric acute myeloid leukemia
Language English Country United States Media print
Document type Journal Article
PubMed
27351222
PubMed Central
PMC5217027
DOI
10.18632/oncotarget.10270
PII: 10270
Knihovny.cz E-resources
- Keywords
- MLL, acute myeloid leukemia, miR-106b~25, relapse,
- MeSH
- Leukemia, Myeloid, Acute genetics pathology MeSH
- Child MeSH
- Histone-Lysine N-Methyltransferase genetics metabolism MeSH
- Introns genetics MeSH
- Carcinogenesis genetics MeSH
- Clonal Evolution MeSH
- Cohort Studies MeSH
- Infant MeSH
- Humans MeSH
- Neoplasm Recurrence, Local genetics pathology MeSH
- Minichromosome Maintenance Complex Component 7 metabolism MeSH
- RNA, Messenger metabolism MeSH
- MicroRNAs genetics MeSH
- Adolescent MeSH
- Multigene Family MeSH
- Child, Preschool MeSH
- Myeloid-Lymphoid Leukemia Protein genetics MeSH
- Gene Expression Regulation, Leukemic * MeSH
- Gene Expression Profiling MeSH
- E2F1 Transcription Factor metabolism MeSH
- Translocation, Genetic MeSH
- Up-Regulation MeSH
- Check Tag
- Child MeSH
- Infant MeSH
- Humans MeSH
- Adolescent MeSH
- Male MeSH
- Child, Preschool MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- E2F1 protein, human MeSH Browser
- Histone-Lysine N-Methyltransferase MeSH
- KMT2A protein, human MeSH Browser
- Minichromosome Maintenance Complex Component 7 MeSH
- MCM7 protein, human MeSH Browser
- RNA, Messenger MeSH
- MicroRNAs MeSH
- MIRN106 microRNA, human MeSH Browser
- Myeloid-Lymphoid Leukemia Protein MeSH
- E2F1 Transcription Factor MeSH
The most important reason for therapy failure in pediatric acute myeloid leukemia (AML) is relapse. In order to identify miRNAs that contribute to the clonal evolution towards relapse in pediatric AML, miRNA expression profiling of 127 de novo pediatric AML cases were used. In the diagnostic phase, no miRNA signatures could be identified that were predictive for relapse occurrence, in a large pediatric cohort, nor in a nested mixed lineage leukemia (MLL)-rearranged pediatric cohort. AML with MLL- rearrangements are found in 15-20% of all pediatric AML samples, and reveal a relapse rate up to 50% for certain translocation partner subgroups. Therefore, microRNA expression profiling of six paired initial diagnosis-relapse MLL-rearranged pediatric AML samples (test cohort) and additional eight paired initial diagnosis-relapse samples with MLL-rearrangements (validation cohort) was performed. A list of 53 differentially expressed miRNAs was identified of which the miR-106b~25 cluster, located in intron 13 of MCM7, was the most prominent. These differentially expressed miRNAs however could not predict a relapse in de novo AML samples with MLL-rearrangements at diagnosis. Furthermore, higher mRNA expression of both MCM7 and its upstream regulator E2F1 was found in relapse samples with MLL-rearrangements. In conclusion, we identified the miR-106b~25 cluster to be upregulated in relapse pediatric AML with MLL-rearrangements.
Clinic for Pediatrics 3 University Hospital Essen Essen Germany
Department of Hematology Hopital Saint Louis Paris France
Department of Pediatric Hematology and Oncology Hannover Medical School Hannover Germany
Dutch Childhood Oncology Group The Hague The Netherlands
Paediatric Oncology Haematology VU University Medical Centre Amsterdam The Netherlands
Princess Maxima Center for Pediatric Oncology Utrecht The Netherlands
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