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Updated: Nov 30, 2025

In Vitro Selection of Engineered Transcriptional Repressors for Targeted Epigenetic Silencing
Published on: May 5, 2023
Epigenome engineering: new technologies for precision medicine.
Agustin Sgro1,2, Pilar Blancafort1,2,3
1Cancer Epigenetics Laboratory, The Harry Perkins Institute of Medical Research, Nedlands, Western Australia 6009, Australia.
Precision epigenome editing using CRISPR/dCas9/12a offers a promising strategy to restore normal cellular function in diseases. This approach aims to overcome limitations of current epigenetic inhibitors for targeted gene therapy.
Area of Science:
- Epigenetics and molecular biology
- Gene editing technologies
- Cancer therapeutics
Background:
- Epigenetic marks regulate chromatin structure and gene expression.
- Approved epigenetic inhibitors have limitations in specificity and toxicity.
- CRISPR/dCas9/12a technology enables precise epigenome manipulation.
Purpose of the Study:
- To review state-of-the-art epigenome editing approaches for disease treatment.
- To highlight methods for engineering and delivering epigenetic effectors.
- To discuss the potential of locus-specific epigenome modification in personalized medicine.
Main Methods:
- Focus on CRISPR/dCas9/12a-based epigenome editing strategies.
- Review of biomolecular engineering for assembling and regulating epigenetic effectors.
- Discussion of delivery methods for therapeutic applications.
Main Results:
- Epigenome editing can reprogram diseased cells towards a normal-like state.
- CRISPR/dCas9/12a offers locus-specificity for targeted epigenetic modification.
- Engineering multiple effectors can enhance therapeutic longevity.
Conclusions:
- CRISPR/dCas9/12a epigenome editing is a promising frontier in precision medicine.
- Further development is needed to address targeting efficiency and intracellular delivery.
- This technology holds potential for treating neoplasms and other diseases.
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