An Old Dog Has a New Trick: Somatic Exonic Deletions in RUNX1 Are Frequent in AML.
editorial · Level V
Where this comes from
- Record sourced from PubMed, PMID 37289016.
- Also identified by DOI 10.1158/1078-0432.CCR-23-1065 and PMC identifier 10525005.
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Abstract
Somatic loss-of-function RUNX1 mutations in acute myeloid leukemia (AML) include missense, nonsense, and frameshift mutations, whereas germline RUNX1 variants in RUNX1-FPDMM also include large exonic deletions. Alternative variant detection approaches revealed that large exonic deletions in RUNX1 are also common in sporadic AML, which has implications for patient stratification and therapeutic decision-making. See related article by Eriksson et al., p. 2826.
Medical subject headings
- Core Binding Factor Alpha 2 Subunit
- Leukemia, Myeloid, Acute