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Updated: May 25, 2025

Flow Cytometry to Estimate Leukemia Stem Cells in Primary Acute Myeloid Leukemia and in Patient-derived-xenografts, at Diagnosis and Follow Up
Published on: March 26, 2018
PTK7 helps detect T lymphoblastic leukemia/lymphoma by flow cytometry
Jonah Maggard1, Yu Yang2, Joanna Chaffin2
1University of Florida College of Medicine, Gainesville, Florida, USA.
Protein tyrosine kinase-7 (PTK7) is a valuable marker for diagnosing T-ALL and detecting minimal residual disease (MRD). PTK7 is expressed in most T-ALL cases and remains detectable at relapse, making it useful for T-ALL flow cytometry panels.
Area of Science:
- Hematology
- Immunology
- Oncology
Background:
- T-cell acute lymphoblastic leukemia/lymphoma (T-ALL) is a cancer of immature T cells.
- Flow cytometry identifies T-ALL by detecting aberrant antigen expression.
- A reliable marker for T-ALL diagnosis and monitoring is needed.
Purpose of the Study:
- To evaluate the utility of protein tyrosine kinase-7 (PTK7) in T-ALL diagnosis, minimal/measurable residual disease (MRD) detection, and relapse monitoring.
- To assess PTK7 expression in T-ALL patient samples using flow cytometry.
Main Methods:
- Retrospective analysis of flow cytometry data from 175 T-ALL patients.
- Evaluation of PTK7 expression at initial diagnosis, MRD, and relapse.
- Comparison of PTK7 expression levels in T-ALL cases versus mature T cells.
Main Results:
- PTK7 was positive in 87.76% of T-ALL cases at diagnosis, 75% at MRD, and 100% at relapse.
- PTK7 expression remained consistent in CD34/TdT negative T-ALL.
- PTK7 expression showed a decrease at MRD but remained intact at relapse.
Conclusions:
- PTK7 is a highly effective marker for T-ALL diagnosis and MRD detection.
- PTK7 should be incorporated into flow cytometry panels for T-ALL evaluation.
- PTK7 aids in monitoring disease status from diagnosis through relapse.
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