# Roles of Extracellular Vesicle-Derived microRNAs in Metabolic Dysfunction-Associated Steatotic Liver Disease to Hepatocellular Carcinoma

**Authors:** Xinlei Ma, Wei Zheng, Chensi Wu, Chengan Xu, Xin Ji, Keyang Xu, Qiaoqiao Yin

PMC · DOI: 10.3390/biomedicines14030528 · Biomedicines · 2026-02-26

## TL;DR

This paper reviews how microRNAs in extracellular vesicles may help diagnose and treat liver disease linked to metabolic dysfunction and liver cancer.

## Contribution

The paper systematically reviews the stage-specific roles of EV-derived miRNAs in MASLD and MASLD-associated HCC, highlighting their potential as biomarkers and therapeutic targets.

## Key findings

- EV-derived miRNAs regulate lipid metabolism and inflammation in MASLD.
- EV-miRNAs influence hepatic stellate cell activation and tumor microenvironment remodeling.
- EV-derived miRNAs show promise as non-invasive biomarkers and therapeutic targets for MASLD-associated HCC.

## Abstract

Metabolic dysfunction-associated steatotic liver disease (MASLD) is a leading cause of chronic liver disease, and has emerged as a common etiological factor for hepatocellular carcinoma (HCC). MASLD and MASLD-associated HCC lack specific clinical biomarkers. Extracellular vesicles (EVs) and their microRNA (miRNA) cargo have emerged as key mediators of intercellular communication and promising diagnostic tools. This review provides a systematic overview of the stage-specific roles of EV-derived miRNAs across the MASLD spectrum. We focus on how key EV-miRNAs regulate lipid metabolism, inflammatory responses, hepatic stellate cell (HSC) activation, and the remodeling of the tumor microenvironment (TME). This review provides an updated perspective on cross-stage EV-derived miRNA regulatory circuits. In addition, we critically evaluate the potential of EV-derived miRNAs as non-invasive biomarkers and therapeutic targets. By integrating mechanistic insights with clinical relevance, this review provides a comprehensive framework for the early identification, risk stratification, and precision intervention of MASLD-associated HCC.

## Linked entities

- **Diseases:** Metabolic dysfunction-associated steatotic liver disease (MONDO:0013209), hepatocellular carcinoma (MONDO:0007256)

## Full-text entities

- **Diseases:** tumor (MESH:D009369), inflammatory (MESH:D007249), MASLD (MESH:D008107), HCC (MESH:D006528)
- **Chemicals:** lipid (MESH:D008055)

## Full text

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## Figures

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## References

116 references — full list in the complete paper: https://tomesphere.com/paper/PMC13024532/full.md

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Source: https://tomesphere.com/paper/PMC13024532