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Updated: Aug 29, 2025

Dual CRISPR-Interference Strategy for Targeting Synthetic Lethal Interactions Between Non-Coding RNAs in Cancer Cells
Published on: May 30, 2025
Stimuli-responsive delivery strategies for controllable gene editing in tumor therapeutics
Yu Ji1, Liansheng Fan1, Suchen Qu1
1Jiangsu Collaborative Innovation Center of Chinese Medicinal Resources Industrialization, Department of Biochemistry and Molecular Biology, School of Medicine & Holistic Integrative Medicine, Nanjing University of Chinese Medicine, Nanjing 210023, China. xhan0220@njucm.edu.cn.
Abstract:
The CRISPR system has attracted significant attention due to its great potential in tumor therapy. Developing effective, precise and safe delivery vectors is a prerequisite for CRISPR applications. Some disease-related biological signals provide a rationale for the development of precise delivery vehicles for stimuli-response delivery. Therefore, combining the linker of endogenous signal and exogenous signal stimulus responses with the nanocarrier is the key to designing and synthesizing the controllable release vector in stimuli-response delivery. This review summarizes the synthesis of stimuli-responsive nanocarriers by designing key chemical structures to achieve controllable release. Nanocarriers controlled by biochemical or physical signals are then discussed. Finally, potential challenges and prospects for existing nanocarriers are discussed.
Insights
CRISPR delivery systems are crucial for tumor therapy. This review details stimuli-responsive nanocarriers designed for precise, controllable drug release, enhancing CRISPR
Area of Science:
- Biomedical Engineering
- Nanotechnology
- Molecular Biology
Background:
- CRISPR technology shows promise for cancer treatment.
- Effective delivery vectors are essential for CRISPR applications.
- Stimuli-responsive systems offer precise targeting for drug delivery.
Purpose of the Study:
- To review the synthesis of stimuli-responsive nanocarriers for CRISPR delivery.
- To discuss nanocarriers controlled by biochemical and physical signals.
- To explore challenges and future prospects in nanocarrier development.
Main Methods:
- Review of literature on stimuli-responsive nanocarrier synthesis.
- Analysis of chemical structures enabling controllable release.
- Discussion of nanocarrier control mechanisms (biochemical/physical signals).
Main Results:
- Key chemical structures for stimuli-responsive nanocarriers are identified.
- Nanocarriers can be designed for controlled release triggered by specific signals.
- Both biochemical and physical stimuli can be utilized for nanocarrier activation.
Conclusions:
- Stimuli-responsive nanocarriers are vital for precise CRISPR-based tumor therapy.
- Designing nanocarriers with specific signal responses is key to controllable release.
- Further research is needed to overcome challenges and advance nanocarrier technology.
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