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Published on: November 10, 2017
Differential protein analysis of lymphocytes between children with acute lymphoblastic leukemia and healthy children
Dao Wang1, Yan-qi Lv, Yu-feng Liu
1Department of Pediatrics, the First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Insights
Researchers identified eight differential proteins in childhood acute lymphoblastic leukemia (c-ALL) patients compared to healthy children. These proteins, with varying expression levels, show potential as new diagnostic markers and therapeutic targets for c-ALL.
Area of Science:
- Proteomics
- Oncology
- Pediatric Hematology
Background:
- Childhood acute lymphoblastic leukemia (c-ALL) is a significant pediatric cancer.
- Identifying specific biomarkers for c-ALL is crucial for early diagnosis and targeted therapy.
Purpose of the Study:
- To identify differentially expressed proteins in lymphocytes of children with c-ALL compared to healthy controls.
- To explore the potential of these identified proteins as novel diagnostic markers and therapeutic targets for c-ALL.
Main Methods:
- Comparative proteomics analysis using two-dimensional gel electrophoresis.
- Protein identification via matrix-assisted laser desorption ionization/time of flight mass spectrometry (MALDI-TOF-MS).
- Analysis of bone marrow lymphocytes from c-ALL patients and peripheral blood lymphocytes from healthy children.
Main Results:
- Fifteen differentially expressed proteins were initially detected between c-ALL and healthy samples.
- Eight proteins were successfully identified, with two showing higher expression and six showing lower expression in c-ALL cells.
- These eight proteins represent significant molecular differences in c-ALL.
Conclusions:
- The identified eight differential proteins hold promise as potential new diagnostic markers for c-ALL.
- These proteins may also serve as future drug targets for the treatment of childhood acute lymphoblastic leukemia.
Abstract:
We identified differential proteins in lymphocytes between patients with childhood acute lymphoblastic leukemia (c-ALL) and healthy children. Samples of bone marrow lymphocytes from children with c-ALL and peripheral blood lymphocytes from healthy children were collected, and total proteins were extracted and separated from these samples followed by two-dimensional gel electrophoresis for comparative analysis. The differential protein spots in c-ALL cells were digested in situ, and then analyzed with matrix-assisted laser desorption ionization/time of flight mass spectrometry (MALDI-TOF-MS) followed by identification using the relevant database. Fifteen differential expression proteins were obtained by comparative proteomics analysis. Of the 15 differential proteins, eight were identified. Of the eight proteins, two had high expression and six low expression in c-ALL cells. The eight differential proteins are expected to become new diagnostic markers and drug targets for c-ALL.
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