Related Experiment Video
Updated: May 20, 2026

Designing a Bio-responsive Robot from DNA Origami
Published on: July 8, 2013
DNA origami as a carrier for circumvention of drug resistance
Qiao Jiang1, Chen Song, Jeanette Nangreave
1National Center for NanoScience and Technology, 11 BeiYiTiao, ZhongGuanCun, 100190 Beijing, China.
Abstract:
Although a multitude of promising anti-cancer drugs have been developed over the past 50 years, effective delivery of the drugs to diseased cells remains a challenge. Recently, nanoparticles have been used as drug delivery vehicles due to their high delivery efficiencies and the possibility to circumvent cellular drug resistance. However, the lack of biocompatibility and inability to engineer spatially addressable surfaces for multi-functional activity remains an obstacle to their widespread use. Here we present a novel drug carrier system based on self-assembled, spatially addressable DNA origami nanostructures that confronts these limitations. Doxorubicin, a well-known anti-cancer drug, was non-covalently attached to DNA origami nanostructures through intercalation. A high level of drug loading efficiency was achieved, and the complex exhibited prominent cytotoxicity not only to regular human breast adenocarcinoma cancer cells (MCF 7), but more importantly to doxorubicin-resistant cancer cells, inducing a remarkable reversal of phenotype resistance. With the DNA origami drug delivery vehicles, the cellular internalization of doxorubicin was increased, which contributed to the significant enhancement of cell-killing activity to doxorubicin-resistant MCF 7 cells. Presumably, the activity of doxorubicin-loaded DNA origami inhibits lysosomal acidification, resulting in cellular redistribution of the drug to action sites. Our results suggest that DNA origami has immense potential as an efficient, biocompatible drug carrier and delivery vehicle in the treatment of cancer.
Insights
DNA origami nanostructures efficiently deliver anti-cancer drugs like doxorubicin, overcoming drug resistance in cancer cells. This biocompatible system enhances drug uptake and cell-killing activity, showing promise for cancer treatment.
Area of Science:
- Biotechnology
- Nanotechnology
- Cancer Research
Background:
- Effective anti-cancer drug delivery remains a challenge despite numerous drug developments.
- Nanoparticles offer high delivery efficiency and can bypass cellular drug resistance.
- Limitations of current nanoparticles include poor biocompatibility and lack of surface engineerability.
Purpose of the Study:
- To develop a novel drug carrier system using DNA origami nanostructures.
- To address limitations of current nanoparticle drug delivery systems.
- To evaluate the efficacy of DNA origami as a biocompatible and spatially addressable drug carrier.
Main Methods:
- Doxorubicin was attached to DNA origami nanostructures via intercalation.
- Cytotoxicity was assessed using regular (MCF 7) and doxorubicin-resistant cancer cells.
- Cellular internalization and drug redistribution mechanisms were investigated.
Main Results:
- High drug loading efficiency was achieved with DNA origami nanostructures.
- The drug-loaded nanostructures demonstrated significant cytotoxicity against both regular and resistant cancer cells.
- A remarkable reversal of drug resistance phenotype was observed in resistant cancer cells.
- Increased cellular internalization of doxorubicin by DNA origami enhanced cell-killing activity.
Conclusions:
- DNA origami nanostructures show immense potential as efficient and biocompatible drug carriers.
- This novel system effectively delivers anti-cancer drugs and overcomes cellular drug resistance.
- DNA origami holds promise for advanced cancer treatment strategies.
Related Concept Videos
Treatment Resistant Cancers
DNA Damage can Stall the Cell Cycle
Experimental RNAi
Site-Targeted Drug Delivery Systems: Polymeric Carriers
RNA Interference
This process occurs naturally in cells, often through the activity of genomically-encoded microRNAs. Researchers can take advantage of this mechanism by introducing synthetic RNAs to deactivate specific genes for research or therapeutic purposes. For example, RNAi could be used...

