Nanoparticulate RNA delivery systems in cancer
Related Experiment Video
Updated: Dec 13, 2025

Preparation of Neutrally-charged, pH-responsive Polymeric Nanoparticles for Cytosolic siRNA Delivery
Published on: May 2, 2019
Ankur Sharma1, Niraj Kumar Jha2, Kajal Dahiya1
1Department of Life Science, School of Basic Science & Research, Sharda University, Greater Noida, India.
Background:
Drug delivery system is a common practice in cancer treatment. RNA interference-mediated post-transcriptional gene silencing holds promise as an approach to knockdown in the expression of target genes responsible for cancer cell growth and metastasis. RNA interference (RNAi) can be achieved by delivering small interfering RNA (siRNA) and short hairpin RNA (shRNA) to target cells. Since neither interfering RNAs can be delivered in naked form due to poor stability, an efficient delivery system is required that protects, guides, and delivers the siRNA and shRNA to target cells as part of cancer therapy (chemotherapy).
Recent Findings:
In this review, a discussion is presented about the different types of drug delivery system used to deliver siRNA and shRNA, together with an overview of the potential benefits associated with this sophisticated biomolecular therapy. Improved understanding of the different approaches used in nanoparticle (NP) fabrication, along with an enhanced appreciation of the biochemical properties of siRNA/shRNA, will assist in developing improved drug delivery strategies in basic and clinical research.
Conclusion:
These novel delivery techniques are able to solve the problems that form an inevitable part of delivering genes in more efficient manner and as part of more effective treatment protocols. The present review concludes that the nanoparticulate RNA delivery system has great possibility for cancer treatment along with several other proposed methods. Several NPs or nanocarriers are already in use, but the methods proposed here could fulfill the missing gap in cancer research. It is the future technology, which unravels the mystery of resolving genomic diseases that is, especially genomic instability and its signaling cascades.
Insights
Nanoparticle delivery systems offer a promising approach for cancer treatment by enabling RNA interference (RNAi) therapies. These systems protect and deliver small interfering RNA (siRNA) and short hairpin RNA (shRNA) for effective gene silencing.
Area of Science:
- Biomedical Engineering
- Molecular Biology
- Oncology
Background:
- Drug delivery systems are crucial in cancer therapy.
- RNA interference (RNAi) uses small interfering RNA (siRNA) and short hairpin RNA (shRNA) to silence genes driving cancer growth.
- Effective delivery of siRNA/shRNA requires specialized systems due to their instability.
Purpose of the Study:
- To review various drug delivery systems for siRNA and shRNA in cancer therapy.
- To discuss the benefits of advanced biomolecular therapies.
- To highlight the importance of understanding nanoparticle fabrication and siRNA/shRNA properties for improved delivery strategies.
Main Methods:
- Review of existing literature on nanoparticle (NP) fabrication for RNA delivery.
- Analysis of biochemical properties of siRNA/shRNA.
- Discussion of different NP-based delivery systems for RNAi therapeutics.
Main Results:
- Nanoparticulate RNA delivery systems show significant potential for cancer treatment.
- Novel delivery techniques address challenges in gene delivery efficiency and therapeutic protocols.
- Existing NPs and proposed methods can fill gaps in current cancer research.
Conclusions:
- Nanoparticulate RNA delivery systems represent a promising future technology for cancer therapy.
- These systems can help unravel the mechanisms of genomic diseases, including genomic instability.
- Further research into NP fabrication and RNA properties will advance RNAi-based cancer treatments.
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RNA Interference
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In the cytoplasm, siRNA is processed from a double-stranded RNA, which comes from either endogenous DNA transcription or exogenous sources like a virus. This double-stranded RNA is then cleaved by the...

