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Updated: Jun 18, 2026

A Flow Cytometry-Based Cell Surface Protein Binding Assay for Assessing Selectivity and Specificity of an Anticancer Aptamer
Published on: September 13, 2022
Targeted delivery of daunorubicin to T-cell acute lymphoblastic leukemia by aptamer
Seyed Mohammad Taghdisi1, Khalil Abnous, Fatemeh Mosaffa
1Department of Pharmaceutical Biotechnology, Mashhad University of Medical Sciences, Mashhad, Iran.
Abstract:
Application of daunorubicin in treatment of leukemia has been limited for its side effects like cardiotoxicity. Specific delivery of chemotherapy drugs is an important factor in decreasing their side effects. In this study, sgc8, an aptamer for protein tyrosine kinase-7 (PTK7), was used for specific delivery of daunorubicin to Molt-4 cells (PTK7(+)). Flow cytometric experiments showed that aptamer-daunorubicin complex was internalized effectively to Molt-4 cells (PTK7(+)), but not to U266 cells (PTK7(-)). This fact was confirmed by less cytotoxicity of aptamer-drug complex in U266 cells in compare to daunorubicin alone. No significant change in viability between daunorubicin and aptamer-daunorubicin complex treated Molt4 cells was observed. In conclusion, sgc8-daunorubicin complex is introduced as a simple and efficient system for targeted delivery of drug to acute lymphoblastic leukemia T cells.
Insights
This study developed an aptamer-drug complex for targeted delivery of daunorubicin to leukemia cells. The sgc8-daunorubicin complex effectively targeted protein tyrosine kinase-7 positive cells, reducing side effects and improving treatment specificity.
Area of Science:
- Biochemistry
- Pharmacology
- Oncology
Background:
- Daunorubicin is a chemotherapy drug used for leukemia but has cardiotoxicity side effects.
- Targeted drug delivery can minimize chemotherapy-induced toxicity.
- Protein tyrosine kinase-7 (PTK7) is a target for specific cancer cell delivery.
Purpose of the Study:
- To develop a targeted drug delivery system using an aptamer for daunorubicin.
- To evaluate the efficacy and specificity of the sgc8-daunorubicin complex in delivering daunorubicin to leukemia cells.
Main Methods:
- Synthesis of an aptamer-drug complex using sgc8 aptamer and daunorubicin.
- Flow cytometry to assess cellular uptake in PTK7-positive (Molt-4) and PTK7-negative (U266) cells.
- Cytotoxicity assays to compare the efficacy of the complex versus free drug.
Main Results:
- The sgc8-daunorubicin complex showed effective internalization into Molt-4 cells (PTK7(+)).
- Minimal uptake and reduced cytotoxicity were observed in U266 cells (PTK7(-)).
- No significant difference in viability was noted between the complex and free daunorubicin in Molt-4 cells, indicating targeted delivery without compromising efficacy.
Conclusions:
- The sgc8-daunorubicin complex represents a simple and efficient system for targeted drug delivery.
- This approach specifically targets acute lymphoblastic leukemia T cells expressing PTK7.
- The targeted delivery system holds potential for reducing daunorubicin's side effects in leukemia treatment.
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