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Updated: Feb 20, 2026

Dual CRISPR-Interference Strategy for Targeting Synthetic Lethal Interactions Between Non-Coding RNAs in Cancer Cells
Published on: May 30, 2025
CRISPR/Cas9-mediated noncoding RNA editing in human cancers
Jie Yang1,2, Xiaodan Meng1,2, Jinchang Pan1,2
1a Department of Biochemistry and Molecular Biology , Medical School of Ningbo University , Ningbo , Zhejiang , China.
The clustered regularly interspaced short palindromic repeats (CRISPR)-associated nuclease 9 (CRISPR/Cas9) system offers a novel approach for cancer therapy by editing noncoding RNAs (ncRNAs). This technology shows promise for precision oncology and treating human cancers.
Area of Science:
- Genetics
- Molecular Biology
- Oncology
Background:
- Cancer involves genetic and epigenetic changes, with noncoding RNAs (ncRNAs) regulating cancer genes.
- The CRISPR/Cas9 system is a powerful genome-editing tool with potential in ncRNA-based cancer therapy.
Purpose of the Study:
- To review the CRISPR/Cas9 system's classifications, mechanisms, and applications in editing ncRNAs for cancer therapy.
- To discuss novel CRISPR/Cas9-based techniques, off-target effects, and challenges in cancer treatment.
Main Methods:
- Review of CRISPR/Cas9 system classifications and mechanisms.
- Focus on CRISPR/Cas9 applications for editing microRNAs, long noncoding RNAs, and circular RNAs in cancers.
- Evaluation of off-target effects and solutions.
Main Results:
- CRISPR/Cas9 system provides a versatile tool for precise ncRNA editing in cancer research.
- Novel techniques based on CRISPR/Cas9 are emerging for therapeutic applications.
- Understanding and mitigating off-target effects are crucial for clinical translation.
Conclusions:
- CRISPR/Cas9-mediated ncRNA editing represents a promising strategy for precision oncology.
- This technology holds potential for developing novel cancer therapies targeting long and short ncRNAs.
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