Evidence map›Paper›PMID 38299293›Full record

ReviewCurrent medicinal chemistry2025

Liver-derived Exosomal miRNA in NAFLD: Mechanisms of Action, Biomarkers, and Therapeutic Applications.

Jun Yang, Xiaolei Tang, Liang Chen, Junjie Hu, Shan Li, Ming Yuan, Xianxiang Tian, Zhenpeng Qiu

Abstract readReview
PubMed Publisher
In one paragraph

Review in Current medicinal chemistry, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.8field-weighted citation impact, top 30% of its field
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

5 citing papers in PubMed, 2 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Review
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

8 authors at 3 institutions in 1 country.

Jun YangSchool of Pharmacy, Hubei University of Chinese Medicine, 430065, Wuhan, People's Republic of China.
Xiaolei TangTranslational Medicine Center of the Second Affiliated Hospital of Wannan Medical College, 241002, Wuhu, People's Republic of China.ORCID 0000-0002-3751-1643
Liang ChenSchool of Pharmacy, Hubei University of Chinese Medicine, 430065, Wuhan, People's Republic of China.
Junjie HuSchool of Pharmacy, Hubei University of Chinese Medicine, 430065, Wuhan, People's Republic of China.
Shan LiHubei Key Laboratory of Wudang Local Chinese Medicine Research, Hubei University of Medicine, 442000, Shiyan, People's Republic of China.
Ming YuanSchool of Pharmacy, Hubei University of Chinese Medicine, 430065, Wuhan, People's Republic of China.
Xianxiang TianSchool of Pharmacy, Hubei University of Chinese Medicine, 430065, Wuhan, People's Republic of China.
Zhenpeng QiuSchool of Pharmacy, Hubei University of Chinese Medicine, 430065, Wuhan, People's Republic of China.ORCID 0000-0003-2568-8983
Hubei University of Chinese Medicine · CNHubei University of Medicine · CNWannan Medical College · CN

Funding

National Natural Science Foundation of China 82074077Natural Science Foundation of Hubei Province 2022CFB381Open Project of Hubei Key Laboratory of Wudang Local Chinese Medicine Research (Hubei University of Medicine) WDCM2023016
6 · The paper itself

Abstract

Nonalcoholic fatty liver disease (NAFLD) is of global concern due to its high prevalence worldwide. NAFLD, as one of the most common causes of liver function abnormalities, is associated with obesity, insulin resistance, and type 2 diabetes mellitus, and there are no medications available to treat NAFLD. Extracellular vesicles (EVs) are nanosized, membrane-bound vesicles that deliver biomolecules between cells. Exosomes are a subtype of EVs that mediate intercellular communication by delivering proteins and RNAs. MicroRNAs (miRNAs) are a highly conserved class of small tissue-specific non-coding RNAs that influence the expression of many functionally interacting genes. Hepatic-derived exosomal miRNAs are tightly associated with NAFLD occurrence and progression through multiple mechanisms. In addition, the characterization of miRNAs suggests that they may serve as multifunctional biomarkers for NAFLD, be used as clinical therapeutic targets for NAFLD, and be significant predictors of patient prognosis. Here, we review recent advances in the regulation and function of exosome- derived miRNAs in NAFLD, focusing on miRNAs specifically expressed or enriched in hepatocytes (HCs), hepatic macrophages, hepatic stellate cells (HSCs), and other immune cells in the liver. Finally, we discuss future research directions on exosomal miRNAs as biomarkers for NAFLD's diagnosis and clinical therapeutic targets.

Indexed as

ExosomesLiverMicroRNAsNon-alcoholic Fatty Liver DiseaseAnimalsBiomarkersHumansBiomarkersMicroRNAsbiomarker.exosomemicroRNANAFLDNASHsteatosis

Identifiers

PMID38299293
OpenAlexW4391439966

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.