Evidence map›Paper›PMID 41826707›Full record

ArticlePediatric research2026

Identification of the expression of tRNA-derived small RNAs associated with necrotizing enterocolitis.

Jingjing Zhou, Xiying Xiang, Luo Xin, Xueyi Jiang, Ping Li, Dan Yu, Mingyan Hei, Min Jiang

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Article in Pediatric research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

8 authors.

Jingjing ZhouNeonatal Center, Beijing Children's Hospital, Capital Medical University, Beijing, China.
Xiying XiangNeonatal Center, Beijing Children's Hospital, Capital Medical University, Beijing, China.
Luo XinNeonatal Center, Beijing Children's Hospital, Capital Medical University, Beijing, China.
Xueyi JiangNeonatal Center, Beijing Children's Hospital, Capital Medical University, Beijing, China.
Ping LiNeonatal Center, Beijing Children's Hospital, Capital Medical University, Beijing, China.
Dan YuNeonatal Center, Beijing Children's Hospital, Capital Medical University, Beijing, China.
Mingyan HeiNeonatal Center, Beijing Children's Hospital, Capital Medical University, Beijing, China.
Min JiangNeonatal Center, Beijing Children's Hospital, Capital Medical University, Beijing, China. jiangmin7496@sina.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundNecrotizing enterocolitis (NEC) is a severe neonatal gastrointestinal disease. We explored plasma exosomal small noncoding RNAs (sncRNAs), especially tsRNAs, as potential NEC treatment targets.

methodsSmall RNA microarray analysis was performed on exosomes from 4 NEC and 4 control plasma samples, and 9 paired samples were used for qRT-PCR validation. GO and KEGG analyses determined tsRNAs' functions, and TargetScan and miRanda identified their target genes.

resultstsRNAs were prominently altered among sncRNAs. We found 10 downregulated and 4 upregulated tsRNAs in the NEC group. Bioinformatics analysis showed they regulate immune processes via pathways like "Cytokine-cytokine receptor interaction". POU2AF1 expression was significantly upregulated in NEC.

conclusionPlasma-derived exosomal tsRNAs suggest a preliminary association with NEC diagnosis and progression. POU2AF1 represents a potential therapeutic target, but more pre-clinical and clinical studies are required. IMPACT: The expression of sncRNAs in plasma-derived exosomes appears to be altered between neonates with NEC and healthy neonates. We assessed the potential effect of suggestive differential expression of tsRNAs through bioinformatics analysis to explore the key genes influencing the development of NEC. Our findings suggest the possibility that POU2AF1 could serve as a potential biomarker for the treatment of NEC.

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