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Published on: August 11, 2022
Anti-MUC1 Aptamer as Carrier Tool of the Potential Radiosensitizer 1,10 Phenanthroline in MCF-7 Breast Cancer Cells
Laís N Alves1,2, Sotiris Missailidis2, Claudia A S Lage3
1Laboratory of Radiobiology, Division of Medical Physics, Institute of Radioprotection and Dosimetry, Brazilian Nuclear Energy Commission, Rio de Janeiro, Brazil.
Background:
Proteins overexpressed in malignant tissues form important targets in the development of targeted therapeutics, and aptamers comprise an important affinity agent for therapy and drug delivery. In this study, aberrantly expressed mucin 1 glycoprotein was investigated as a therapeutic target in a breast cancer model.
Materials And Methods:
In order to determine the feasibility of using an aptamer against mucin 1 (aptA) as carrier of the cytotoxic compound 1,10-phenanthroline to MCF-7 cells, as a potential radiosensitizer, was studied in experiments using circular dichroism and rhodamine labelling by fluorescent microscopy and flow cytometry.
Results:
1,10-Phenanthroline can be intercalated within aptA when complexed with Fe(II) ions, with dissociation constant (Kd) of 30 μM. The complex was subsequently capable of binding to and being internalised in MCF-7 breast cancer cells.
Conclusion:
aptA can carry 1,10-phenanthroline to cancer cells specifically and this complex represents a potential target-directed anticancer therapy.
Insights
Aptamers targeting Mucin 1 (aptA) can deliver the cytotoxic compound 1,10-phenanthroline to breast cancer cells. This targeted delivery shows potential for novel anticancer therapies.
Area of Science:
- Biochemistry
- Molecular Biology
- Cancer Research
Background:
- Aberrantly expressed Mucin 1 glycoprotein is a key target in breast cancer.
- Aptamers are valuable affinity agents for targeted therapeutics and drug delivery.
Purpose of the Study:
- To investigate the feasibility of using an aptamer against Mucin 1 (aptA) to deliver 1,10-phenanthroline to MCF-7 breast cancer cells.
- To evaluate the potential of this complex as a radiosensitizer.
Main Methods:
- Circular dichroism spectroscopy
- Rhodamine labeling
- Fluorescent microscopy
- Flow cytometry
Main Results:
- 1,10-Phenanthroline intercalated within aptA when complexed with Fe(II) ions (Kd = 30 μM).
- The aptA-phenanthroline complex effectively bound to and was internalized by MCF-7 breast cancer cells.
Conclusions:
- The aptA-phenanthroline complex demonstrates specific delivery of the cytotoxic compound to cancer cells.
- This targeted complex represents a promising strategy for anticancer therapy.
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