Evidence map›Paper›PMID 33300279›Full record

ArticleJournal of cellular and molecular medicine2021

Intestinal epithelial cells related lncRNA and mRNA expression profiles in dextran sulphate sodium-induced colitis.

Huan Liu, Teming Li, Shizhen Zhong, Min Yu, Wenhua Huang

Open access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.8field-weighted citation impact, top 7% 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

18 citing papers in PubMed, 42 citations in OpenAlex.

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  7. Intestinal Epithelial Cell-Related Alternative Splicing Events in Dextran Sodium Sulfate-Induced Acute Colitis.The Turkish journal of gastroenterology : the official journal of Turkish Society of Gastroenterology · 2023
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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

5 authors at 4 institutions in 1 country.

Huan LiuThe Precision Medicine Institute, The Third Affiliated Hospital, Southern Medical University, Guangzhou, China.ORCID 0000-0002-5519-7336
Teming LiDepartment of General Surgery, Xinqiao Hospital, Army Medical University, Chongqing, China.
Shizhen ZhongGuangdong Engineering Research Center for Translation of Medical 3D Printing Application, Guangdong Provincial Key Laboratory of Medical Biomechanics, School of Basic Medical Sciences, Southern Medical University, Guangzhou, China.
Min YuDepartment of General Surgery, Xinqiao Hospital, Army Medical University, Chongqing, China.ORCID 0000-0002-8845-8977
Wenhua HuangThe Precision Medicine Institute, The Third Affiliated Hospital, Southern Medical University, Guangzhou, China.
Army Medical University · CNGuangdong Medical College · CNSouthern Medical University · CNSouthwest Medical University · CN

Funding

Luzhou municipal people's government-southwest medical university science and technology strategic cooperation project 2018LZXNYD-ZK19National Natural Science Foundation of China 61427807National Natural Science Foundation of China 81970468Special Fund for High-level Talents (Chen Chen Team) of the People's Government of Luzhou-Southwestern Medical UniversitySpecial Fund for High-level Talents (Shizhen Zhong Team) of the People's Government of Luzhou-Southwestern Medical University
6 · The paper itself

Abstract

Intestinal epithelial barrier damage caused by intestinal epithelial cells (IECs) dysfunction plays a crucial role in the pathogenesis and development of inflammatory bowel disease (IBD). Recently, some studies have suggested the emerging role of long non-coding RNAs (lncRNAs) in IBD. The aim of this study was to reveal lncRNAs and mRNA expression profiles in IECs from a mouse model of colitis and to expand our understanding in the intestinal epithelial barrier regulation. IECs from the colons of wild-type mice and dextran sulphate sodium (DSS)-induced mice were isolated for high-throughput RNA-sequencing. A total of 254 up-regulated and 1013 down-regulated mRNAs and 542 up-regulated and 766 down-regulated lncRNAs were detected in the DSS group compared with the Control group. Four mRNAs and six lncRNAs were validated by real-time quantitative PCR. Function analysis showed that dysregulated mRNAs participated in TLR7 signalling pathway, IL-1 receptor activity, BMP receptor binding and IL-17 signalling pathway. Furthermore, the possibility of indirect interactions between differentially expressed mRNAs and lncRNAs was illustrated by the competing endogenous RNA (ceRNA) network. LncRNA ENSMUST00000128026 was predicted to bind to mmu-miR-6899-3p, regulating Dnmbp expression. LncRNA NONMMUT143162.1 was predicted to competitively bind to mmu-miR-6899-3p, regulating Tnip3 expression. Finally, the protein-protein interaction (PPI) network analysis was constructed with 311 nodes and 563 edges. And the highest connectivity degrees were Mmp9, Fpr2 and Ccl3. These results provide novel insights into the functions of lncRNAs and mRNAs involved in the regulation of the intestinal epithelial barrier.

Indexed as

Gene Expression ProfilingGene Expression RegulationAnimalsColitisDextran SulfateEpithelial CellsGene OntologyGene Regulatory NetworksIntestinesMaleMiceMice, Inbred C57BLMolecular Sequence AnnotationProtein Interaction MapsReproducibility of ResultsRNA, Long NoncodingDextran SulfateRNA, Long NoncodingRNA, Messengerinflammatory bowel diseaseintestinal epithelial barrierintestinal epithelial cellslncRNAsmRNAs

Identifiers

PMID33300279
PMCPMC7812259
OpenAlexW3110961658

What OpenQuestion holds

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LicenceCC BY
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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.