ŠESTÁKOVÁ, Šárka, Zdeněk KREJČÍK, Adam FOLTA, Eva CEROVSKÁ, Cyril ŠÁLEK, Michaela MERKEROVÁ DOSTÁLOVÁ, Pavla PECHERKOVÁ, Zdeněk RÁČIL, Jiří MAYER, Petr CETKOVSKÝ and Hana REMEŠOVÁ. DNA methylation and hydroxymethylation patterns in acute myeloid leukemia patients with mutations in DNMT3A and IDH1/2 and their combinations. Cancer Biomarkers. Amsterdam: IOS Press, 2019, vol. 25, No 1, p. 43-51. ISSN 1574-0153. Available from: https://dx.doi.org/10.3233/CBM-182176.
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Basic information
Original name DNA methylation and hydroxymethylation patterns in acute myeloid leukemia patients with mutations in DNMT3A and IDH1/2 and their combinations
Authors ŠESTÁKOVÁ, Šárka (203 Czech Republic), Zdeněk KREJČÍK (203 Czech Republic), Adam FOLTA (203 Czech Republic), Eva CEROVSKÁ (203 Czech Republic), Cyril ŠÁLEK (203 Czech Republic), Michaela MERKEROVÁ DOSTÁLOVÁ (203 Czech Republic), Pavla PECHERKOVÁ (203 Czech Republic), Zdeněk RÁČIL (203 Czech Republic, belonging to the institution), Jiří MAYER (203 Czech Republic, belonging to the institution), Petr CETKOVSKÝ (203 Czech Republic) and Hana REMEŠOVÁ (203 Czech Republic, guarantor).
Edition Cancer Biomarkers, Amsterdam, IOS Press, 2019, 1574-0153.
Other information
Original language English
Type of outcome Article in a journal
Field of Study 30204 Oncology
Country of publisher Netherlands
Confidentiality degree is not subject to a state or trade secret
WWW URL
Impact factor Impact factor: 3.436
RIV identification code RIV/00216224:14110/19:00108493
Organization unit Faculty of Medicine
Doi http://dx.doi.org/10.3233/CBM-182176
UT WoS 000469000100005
Keywords in English AML; DNMT3A and IDH1/2 mutations; methylation; hydroxymethylation; GZMB; CHFR
Tags 14110212, rivok
Tags International impact, Reviewed
Changed by Changed by: Mgr. Tereza Miškechová, učo 341652. Changed: 11/5/2020 09:46.
Abstract
BACKGROUND: Aberrant epigenetic patterns are a hallmark of acute myeloid leukemia (AML). Mutations in profound epigenetic regulators DNMT3A and IDH1/2 often occur concurrently in AML. OBJECTIVES: The aim was to analyze DNA methylation, hydroxymethylation and mRNA expression profiles in AML with mutations in DNMT3A and IDH1/2 (individually and in combinations). METHODS: Infinium MethylationEPIC BeadChip (Illumina) covering 850,000 CpGs was utilized. The validation of hydroxy-/methylation data was done by pyrosequencing. HumanHT-12 v4 Expression BeadChip (Illumina) was used for expression examination. RESULTS: Hierarchical clustering analysis of DNA hydroxy-/methylation data revealed clusters corresponding to DNMT3A and IDH1/2 mutations and CD34+ healthy controls. Samples with concurrent presence of DNMT3A and IDH1/2 mutations displayed mixed DNA hydroxy-/methylation profile with preferential clustering to healthy controls. Numbers and levels of DNA hydroxymethylation were low. Uniformly hypermethylated loci in AML patients with IDH1/2 mutations were enriched for immune response and apoptosis related genes, among which hypermethylation of granzyme B (GZMB) was found to be associated with inferior overall survival of AML patients (P = 0.035). CONCLUSIONS: Distinct molecular background results in specific DNA hydroxy-/methylation profiles in AML. Site-specific DNA hydroxymethylation changes are much less frequent in AML pathogenesis compared to DNA methylation. Methylation levels of enhancer located upstream GZMB gene might contribute to AML prognostication models.
Links
NV15-25809A, research and development projectName: Národní program studia mutací a klonality leukemických buněk u pacientů s akutní myeloidní leukémií
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