Evidence map›Paper›PMID 42218371›Full record

ArticleBMC immunology2026

The LncRNA MIAT acts as a sponge for miR-942-5p to exacerbate the inflammation and oxidative stress in macrophages during sepsis-associated liver injury.

Juanjuan Shi, Zhiyuan Liu, Juan Liu, Enming Shi

Abstract read
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Article in BMC immunology, 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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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Juanjuan ShiDepartment of Critical Care Medicine, Qiannan Buyi and Miao Autonomous Prefecture People's Hospital, Qiannan, 558000, China.
Zhiyuan LiuDepartment of Critical Care Medicine, Qiannan Buyi and Miao Autonomous Prefecture People's Hospital, Qiannan, 558000, China.
Juan LiuDepartment of Critical Care Medicine, Qiannan Buyi and Miao Autonomous Prefecture People's Hospital, Qiannan, 558000, China.
Enming ShiDepartment of Critical Care Medicine, The Second Affiliated Hospital of Fujian Medical University, No. 34, Zhongshan North Road, Licheng District, Quanzhou, 362000, China. EnmingShidr@163.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSepsis-associated liver injury (SALI) is a risk factor for high mortality in patients with sepsis. However, the pathological mechanism and treatment strategies of SALI remain unclear. This study aims to explore the influence of lncRNA MIAT expression on SALI.

resultsThe MIAT and TXNIP levels in the serum of SALI patients, RAW264.7 stimulated by LPS, and AML-12 co-cultured with RAW264.7 were increased, while miR-942-3p expression was decreased. The secretion level of inflammatory factors, the ROS positive rate, and the MDA content were increased, while the GSH levels and SOD enzymatic activity were reduced in LPS-stimulated RAW264.7. The activity of AML-12 was decreased, and the LDH level was increased. When the MIAT was inhibited, the above results showed opposite trends. MIAT was a molecular sponge for miR-942-5p and represses its activity. After inhibiting miR-942-5p, the inflammatory response and the oxidative stress level were enhanced in LPS-stimulated RAW264.7 and the damage of AML-12 was worsened.

conclusionsThe silence of MIAT alleviated the inflammatory response and oxidative stress in LPS-induced RAW264.7 and alleviated the damage of AML-12 cells by adsorbing miR-942-5p.

Indexed as

InflammationLiver DiseasesMacrophagesMicroRNAsRNA, Long NoncodingSepsisAnimalsHumansLipopolysaccharidesMaleMiceOxidative StressRAW 264.7 CellsRNA, Competitive EndogenousLipopolysaccharidesMiat long non-coding RNAMicroRNAsMIRN942 microRNA, humanRNA, Competitive EndogenousRNA, Long NoncodingInflammationLncRNA MIATmiR-942-5pOxidative stressSepsis-associated liver injury

Identifiers

PMID42218371
PMCPMC13435635

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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.