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Published on: February 21, 2025
Aptamer-mediated cancer gene therapy
Dongxi Xiang, Sarah Shigdar, Greg Qiao
1Dalian 6th People's Hospital, 269 Guibai Road, Dalian, Liaoning, The People's Republic of China, 116031. wduan@deakin.edu.au.
Abstract:
Cancer as a genetic disorder is one of the leading causes of death worldwide. Conventional anticancer options such as chemo- and/or radio-therapy have their own drawbacks and could not provide a cure in most cases at present. More effective therapeutic strategies with less side effects are urgently needed. Aptamers, also known as chemical antibodies, are single strand DNA or RNA molecules that can bind to their target molecules with high affinity and specificity. Such site-specific binding ability of aptamers facilitates the delivery and interaction of exogenous nucleic acids with diseased genes. Thus, aptamer-guided gene therapy has emerged as a promising anticancer strategy in addition to the classic treatment regimen. Aptamers can directly deliver anti-cancer nucleic acids, e.g. small interfering RNA, micro RNA, antimicroRNA and small hairpin RNA, to cancer cells or function as a targeting ligand to guide nanoparticles containing therapeutic nucleic acids. This review focuses on recent progress in aptamer-mediated gene therapy for the treatment of hepatocellular carcinoma and other types of cancers, shedding light on the potential of this novel approach of targeted cancer gene therapy.
Insights
Aptamer-guided gene therapy offers a promising new strategy for treating cancer by delivering therapeutic nucleic acids directly to cancer cells. This approach targets genetic disorders with higher efficacy and fewer side effects than conventional treatments.
Area of Science:
- Biotechnology
- Molecular Biology
- Oncology
Background:
- Cancer is a leading global cause of death, often treated with conventional therapies like chemotherapy and radiotherapy, which have significant drawbacks.
- There is an urgent need for more effective cancer treatments with reduced side effects.
Purpose of the Study:
- To review recent advancements in aptamer-mediated gene therapy for hepatocellular carcinoma and other cancers.
- To highlight the potential of aptamer-guided gene therapy as a novel targeted cancer treatment.
Main Methods:
- Aptamers (single-stranded DNA or RNA molecules) are utilized for their high-affinity and specific binding to target molecules.
- Aptamers facilitate the targeted delivery of therapeutic nucleic acids (e.g., siRNA, miRNA) to cancer cells.
- Aptamers can also guide nanoparticles carrying therapeutic nucleic acids.
Main Results:
- Aptamer-guided gene therapy demonstrates potential in targeting cancer cells specifically.
- This approach enables direct delivery of anti-cancer nucleic acids or guides therapeutic nanoparticles.
- Recent progress shows promise for treating hepatocellular carcinoma and other cancers.
Conclusions:
- Aptamer-mediated gene therapy represents a significant advancement in targeted cancer treatment.
- This strategy offers a promising alternative to conventional cancer therapies with potentially fewer side effects.
- Further research into aptamer-guided gene therapy is warranted for its clinical application.
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