Evidence map›Paper›PMID 39701931›Full record

ReviewMolecular medicine (Cambridge, Mass.)2024

Therapeutic potential of human breast milk-derived exosomes in necrotizing enterocolitis.

Si-Jia Di, Xue-Wei Cui, Tian-Jing Liu, Yong-Yan Shi

Abstract readReview
In one paragraph

Review in Molecular medicine (Cambridge, Mass.), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Inhibition of IP6K1 suppresses NPA formation via platelet short-chain polyphosphate polymers in necrotizing enterocolitis.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2026
    Article
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  7. Review
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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

4 authors.

Si-Jia Di *Department of Pediatrics, Shengjing Hospital of China Medical University, Shenyang, 110004, China.
Xue-Wei Cui *Department of Pediatrics, Shengjing Hospital of China Medical University, Shenyang, 110004, China.
Tian-Jing LiuDepartment of Pediatrics, Shengjing Hospital of China Medical University, Shenyang, 110004, China. tjliu@cmu.edu.cn.
Yong-Yan ShiDepartment of Pediatrics, Shengjing Hospital of China Medical University, Shenyang, 110004, China. yyshi@cmu.edu.cn.ORCID 0000-0002-7933-3806

Funding

Key Research and Development Program of Liaoning Province No.2020JH1/10300001National Natural Science Foundation of China No.81801500National Natural Science Foundation of China No.82171709Shengjing Hospital M1392Shengjing Hospital M1415
6 · The paper itself

Abstract

Necrotizing enterocolitis (NEC) is a severe inflammatory and necrotizing disease of the intestine that primarily affects the neonates, particularly premature infants. It has a high incidence of approximately 8.9% in extremely preterm infants, with a mortality rate ranging from 20 to 30%. In recent years, exosomes, particularly those derived from breast milk, have emerged as potential candidates for NEC therapy. Human breast milk-derived exosomes (BME) have been shown to enhance intestinal barrier function, protect intestinal epithelial cells from oxidative stress, promote the proliferation and migration of intestinal epithelial cells, and reduce the severity of experimental NEC models. As a subset of extracellular vesicles, BME possess the membrane structure, low immunogenicity, and high permeability, making them ideal vehicles for the treatment of NEC. Additionally, exosomes derived from various sources, including stem cells, intestinal epithelial cells, plants, and bacteria, have been implicated in the development and protection of intestinal diseases. This article summarizes the mechanisms through which exosomes, particularly BME, exert their effects on NEC and discusses the feasibility and obstacles associated with this novel therapeutic strategy.

Indexed as

Enterocolitis, NecrotizingExosomesMilk, HumanAnimalsHumansInfant, NewbornIntestinal MucosaExosomeHuman breast milk-derived exosomeNecrotizing enterocolitisNeonate

Identifiers

PMID39701931
PMCPMC11656790

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Registered trials

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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.