Prevalence and dynamics of clonal hematopoiesis caused by leukemia-associated mutations in elderly individuals without hematologic disorders
Autor: | Georg Matziolis, Thomas Ernst, Bernd Gruhn, Florian Perner, Jürgen Landschulze, Anna Hinze, Jana Ernst, Jenny Rinke, Danica Midic, Frank Pester, Violetta Müller, Andreas Hochhaus, Florian H. Heidel |
---|---|
Rok vydání: | 2020 |
Předmět: |
Male
Cancer Research Mutation rate Biology medicine.disease_cause Article DNA Methyltransferase 3A Mice Prevalence medicine Leukaemia Animals Humans DNA (Cytosine-5-)-Methyltransferases RNA Messenger Cancer genetics Aged Aged 80 and over Mutation Leukemia Age Factors Hematology medicine.disease Clone Cells Hematopoiesis Haematopoiesis medicine.anatomical_structure Oncology Immunology Humanized mouse Cohort Female Bone marrow Stem cell |
Zdroj: | Leukemia |
ISSN: | 1476-5551 0887-6924 |
DOI: | 10.1038/s41375-020-0869-y |
Popis: | Clonal hematopoiesis is frequently observed in elderly people. To investigate the prevalence and dynamics of genetic alterations among healthy elderly individuals, a cohort of 50 people >80 years was genotyped for commonly mutated leukemia-associated genes by targeted deep next-generation sequencing. A total of 16 somatic mutations were identified in 13/50 (26%) individuals. Mutations occurred at low variant allele frequencies (median 11.7%) and remained virtually stable over 3 years without development of hematologic malignancies in affected individuals. With DNMT3A mutations most frequently detected, another cohort of 160 healthy people spanning all age groups was sequenced specifically for DNMT3A revealing an overall mutation rate of 6.2% (13/210) and an age-dependent increase of mutation prevalence. A significant difference (p = 0.017) in the DNMT3A expression pattern was detected between younger and healthy elderly people as determined by qRT-PCR. To evaluate the selection of clonal hematopoietic stem cells (HSCs), bone marrow of two healthy individuals with mutant DNMT3A was transplanted in a humanized mouse model. Xenografts displayed stable kinetics of DNMT3A mutations over 8 months. These findings indicate that the appearance of low-level clones with leukemia-associated mutations is a common age-associated phenomenon, but insufficient to initiate clonal selection and expansion without the additional influence of other factors. |
Databáze: | OpenAIRE |
Externí odkaz: |