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Updated: Jan 24, 2026

Polyethyleneimine-coated Iron Oxide Nanoparticles as a Vehicle for the Delivery of Small Interfering RNA to Macrophages In Vitro and In Vivo
Published on: February 5, 2019
Dextran-coated iron oxide nanoparticle for delivery of miR-29a to breast cancer cell line
1a Department of Molecular Biology and Genetics , Kırşehir Ahi Evran University , Kırşehir , Turkey.
Abstract:
In the last years, miRNAs have been associated with molecular pathways of cancer and other diseases. The change of expression level of miRNA has an inhibitory role in tumorigenesis. Nevertheless, the poor bioavailability of miRNA due to the rapid enzymatic degradation is a critical handicap in cancer therapy. In this study, we designed dextran-coated iron oxide-based nanoparticle for the delivery of miR-29a to breast cancer cells and analyzed its therapeutic efficacy in vitro. Results indicated that the presence of dextran-coated magnetic nanoparticles, loaded with miR29a, enhanced the selective delivery of miR-29a. Further, miR-29a complex nanoparticles caused down-regulation of anti-apoptotic genes. These results pave the way for further investigations into the possible use of miR-29a complex magnetic nanoparticles for breast cancer therapy.
Insights
Dextran-coated magnetic nanoparticles effectively deliver miR-29a to breast cancer cells, inhibiting tumor growth by down-regulating anti-apoptotic genes. This offers a promising new strategy for breast cancer therapy.
Area of Science:
- Biomedical Engineering
- Nanotechnology
- Oncology
Background:
- MicroRNAs (miRNAs) are implicated in cancer pathways, with altered expression levels potentially inhibiting tumorigenesis.
- Poor miRNA bioavailability due to enzymatic degradation hinders effective cancer therapy.
- Targeted delivery of therapeutic miRNAs remains a significant challenge in oncology.
Purpose of the Study:
- To design and evaluate dextran-coated iron oxide nanoparticles for targeted delivery of miR-29a to breast cancer cells.
- To analyze the therapeutic efficacy of miR-29a-loaded nanoparticles in vitro.
- To investigate the potential of this nanodelivery system for breast cancer treatment.
Main Methods:
- Development of dextran-coated iron oxide nanoparticles.
- Loading of miR-29a onto the nanoparticles.
- In vitro assessment of selective delivery to breast cancer cells.
- Analysis of gene expression, specifically focusing on anti-apoptotic genes.
Main Results:
- The nanoparticles demonstrated enhanced selective delivery of miR-29a to breast cancer cells.
- miR-29a delivered via nanoparticles led to the down-regulation of anti-apoptotic genes.
- The nanocarrier system proved effective in vitro for miRNA delivery.
Conclusions:
- Dextran-coated magnetic nanoparticles are a viable platform for targeted miR-29a delivery in breast cancer.
- This approach shows potential for inhibiting cancer progression by modulating apoptosis-related genes.
- Further research is warranted to explore the clinical application of miR-29a-loaded magnetic nanoparticles in breast cancer therapy.
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