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Updated: Oct 2, 2025

Proliferation and Differentiation of Murine Myeloid Precursor 32D/G-CSF-R Cells
Published on: February 21, 2018
CD26/DPP-4 in Chronic Myeloid Leukemia.
Anna Sicuranza1, Donatella Raspadori2, Monica Bocchia1,2
1Hematology Unit, Department of Medical Science, Surgery and Neuroscience, University of Siena, 53100 Siena, Italy.
CD26 is a specific marker for leukemia stem cells (LSCs) in Chronic Myeloid Leukemia (CML). Monitoring CD26+ LSCs may help track treatment effectiveness in CML patients.
Area of Science:
- Hematology
- Oncology
- Molecular Biology
Background:
- CD26 expression is altered in various cancers.
- CD26 is identified as a specific marker for leukemia stem cells (LSCs) in Chronic Myeloid Leukemia (CML).
- CD26 is absent on normal hematopoietic stem cells and LSCs in other myeloid neoplasms.
Purpose of the Study:
- To investigate CD26 as a specific marker for CML LSCs.
- To evaluate the presence of CD26+ LSCs in CML patients at diagnosis and during treatment.
- To explore the potential of CD26+ LSCs as a biomarker for monitoring therapeutic response in CML.
Main Methods:
- Flow cytometry assays were used to detect CD26 expression on LSCs.
- Peripheral blood (PB) samples from diagnosed Chronic-Phase CML patients were analyzed.
- Analysis included patients undergoing Tyrosine Kinase Inhibitors (TKIs) treatment.
Main Results:
- CD26+ LSCs were detected in all evaluated PB samples of CML patients at diagnosis.
- Circulating CD26+ LSCs were found in most CML patients on TKI treatment, irrespective of molecular response depth.
- Higher numbers of CD26+ LSCs at diagnosis correlated with poorer treatment response in preliminary data.
Conclusions:
- CD26 is confirmed as a specific marker for CML.
- CD26+ LSCs persist during TKI therapy, even with deep molecular responses.
- CD26+ LSCs show potential as a biomarker for monitoring CML therapeutic efficacy.
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