# Epigenetic mechanisms in stem cell therapies for achilles tendinopathy

**Authors:** Zheyang Yuan, Zheyu Yao, Xufeng Mao, Xiang Gao, Sengyi Wu, Haijiao Mao

PMC · DOI: 10.3389/fcell.2025.1516250 · Frontiers in Cell and Developmental Biology · 2025-03-13

## TL;DR

This review explores how epigenetic changes affect stem cell therapies for Achilles tendinopathy, aiming to improve treatment outcomes.

## Contribution

The paper highlights novel epigenetic mechanisms, such as DNA methylation and non-coding RNAs, in stem cell therapies for Achilles tendinopathy.

## Key findings

- Epigenetic modifications influence stem cell proliferation and differentiation in Achilles tendon regeneration.
- Non-coding RNAs like microRNAs and circRNAs regulate gene expression during stem cell therapy.
- Current challenges in stem cell therapies for AT include stability and safety, with potential epigenetic solutions.

## Abstract

Achilles tendinopathy (AT) is a chronic degenerative tendinopathy that affects people’s daily lives. Multiple clinical studies have found that current conservative treatments fail to promote quality tendon healing. Recent studies have found that stem cell therapy can target pathophysiological changes in the tendon by replenishing tendon-derived cells, promoting extracellular matrix (ECM) remodeling, and modulating the inflammatory response to improve the microenvironment of Achilles tendon regeneration. And epigenetic modifications play an important role in stem cell fate determination and function. In this review, we provided a brief overview of the biological properties of relevant stem cells. The influence of epigenetic modifications on stem cell proliferation, differentiation, and immune regulatory function in the treatment of AT was also explored. We focused on gene regulatory mechanisms controlled by DNA methylation, histones and non-coding RNAs including microRNAs, circRNAs and long non-coding RNAs. We also discuss the current challenges faced by stem cell therapies in treating AT and their potential solutions. Further research in this area will provide a more comprehensive epigenetic explanation for stem cell therapy for AT, leading to the development of stable, safe and effective stem cell therapies.

## Full-text entities

- **Diseases:** AT (MESH:D052256), inflammatory (MESH:D007249), degenerative (MESH:D019636)

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11965899/full.md

## References

109 references — full list in the complete paper: https://tomesphere.com/paper/PMC11965899/full.md

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Source: https://tomesphere.com/paper/PMC11965899