Genetic complexity of chronic myelomonocytic leukemia.
Chronic myelomonocytic leukemia
epigenetics
genetics
growth factor
mutation
transcription factors
Journal
Leukemia & lymphoma
ISSN: 1029-2403
Titre abrégé: Leuk Lymphoma
Pays: United States
ID NLM: 9007422
Informations de publication
Date de publication:
05 2021
05 2021
Historique:
pubmed:
19
12
2020
medline:
20
5
2021
entrez:
18
12
2020
Statut:
ppublish
Résumé
In recent years CMML has received increased attention as the most commonly observed MDS/MPN overlap syndrome. Renewed interest has occurred in part due to widespread adoption of next-generation sequencing panels that help render the diagnosis in the absence of morphologic dysplasia. Although most CMML patients exhibit somatic mutations in epigenetic modifiers, spliceosome components, transcription factors and signal transduction genes, it is increasingly clear that a small subset harbors an inherited predisposition to CMML and other myeloid neoplasms. More intriguing is the fact that the mutational spectrum observed in CMML is found in other types of myeloid leukemias, begging the question of how similar genetic backgrounds can lead to such divergent clinical phenotypes. In this review we present a contemporary snapshot of the genetic complexity inherent to CMML, explore the relationship between genotype-phenotype and present a stepwise model of CMML pathogenesis and progression.
Identifiants
pubmed: 33337259
doi: 10.1080/10428194.2020.1856837
doi:
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM