Recognizing Minor Leukemic Populations with Monocytic Features in Mixed-Phenotype Acute Leukemia by Flow Cell Sorting Followed by Cytogenetic and Molecular Studies: Report of Five Exemplary Cases.
Alexandra SemchenkovaSvetlana LebedevaIrina DeminaSvetlana KashporEgor VolchkovElena ZakharovaSergey S LarinYulia OlshanskayaGalina NovichkovaAlexey MaschanMichael MaschanAlexander M PopovPublished in: International journal of molecular sciences (2023)
Mixed-phenotype acute leukemia (MPAL), a rare and heterogeneous category of acute leukemia, is characterized by cross-lineage antigen expression. Leukemic blasts in MPAL can be represented either by one population with multiple markers of different lineages or by several single-lineage populations. In some cases, a major blast population may coexist with a smaller population that has minor immunophenotypic abnormalities and may be missed even by an experienced pathologist. To avoid misdiagnosis, we suggest sorting doubtful populations and leukemic blasts and searching for similar genetic aberrations. Using this approach, we examined questionable monocytic populations in five patients with dominant leukemic populations of B-lymphoblastic origin. Cell populations were isolated either for fluorescence in situ hybridization or for clonality assessment by multiplex PCR or next-generation sequencing. In all cases, monocytic cells shared the same gene rearrangements with dominant leukemic populations, unequivocally confirming the same leukemic origin. This approach is able to identify implicit cases of MPAL and therefore leads to the necessary clinical management for patients.
Keyphrases
- acute myeloid leukemia
- single cell
- genetic diversity
- copy number
- end stage renal disease
- cell therapy
- stem cells
- chronic kidney disease
- genome wide
- cell death
- induced apoptosis
- newly diagnosed
- bone marrow
- peritoneal dialysis
- cell proliferation
- prognostic factors
- real time pcr
- oxidative stress
- dna methylation
- cell cycle arrest
- case control
- cell free