Evidence map›Paper›PMID 42365126›Full record

ReviewCellular and molecular life sciences : CMLS2026

Advances and clinical potential of epigenome editing.

Insung Choi, Sueon Kim, Inwha Baek

Abstract readReview
In one paragraph

Review in Cellular and molecular life sciences : CMLS, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Insung Choi *Department of Regulatory Science, Graduate School, Kyung Hee University, Seoul, 02447, Korea.
Sueon Kim *Department of Regulatory Science, Graduate School, Kyung Hee University, Seoul, 02447, Korea.
Inwha BaekDepartment of Regulatory Science, Graduate School, Kyung Hee University, Seoul, 02447, Korea. ibaek@khu.ac.kr.ORCID http://orcid.org/0000-0003-0330-5910

Funding

Ministry of Science and ICT, South Korea RS-2023-00278378Ministry of Science and ICT, South Korea RS-2025-02217909Ministry of Science and ICT, South Korea RS-2026-25478918
6 · The paper itself

Abstract

Epigenome editing has emerged as a powerful platform to modulate gene expression in a precise and reversible manner. Recent advances have significantly improved the efficiency, specificity, and durability of epigenome editing systems, enabling fine-tuned transcriptional control. Building on these developments, epigenome editing platforms are now being explored for therapeutic applications. In this review, we summarize the evolution of clustered regularly interspaced short palindromic repeats (CRISPR)-based epigenome editing technologies, highlighting key improvements in effector modules. We then discuss the disease models in which epigenome editing has been applied, including monogenic disorders, cancer, neurological diseases, and chronic diseases. These examples demonstrate the broad therapeutic promise of targeted epigenetic modulation across diverse pathological contexts. Finally, we tackle key barriers to clinical translation, including cell-type and chromatin context-specific design, in vivo delivery, and multi-gene targeting for complex disease. Collectively, this review underscores the potential of epigenome editing as a versatile platform for precision medicine.

Indexed as

Epigenesis, GeneticEpigenomeEpigenome EditingAnimalsChromatinCRISPR-Cas SystemsHumansNeoplasmsPrecision MedicineChromatinChromatin landscapeEpigenome editingPrecision medicineTranscriptional controlTranslational medicine

Identifiers

PMID42365126
PMCPMC13582704

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.