Evidence map›Paper›PMID 36632449›Full record

ArticleInternational journal of biological sciences2023

Inhibition of IGF2BP1 attenuates renal injury and inflammation by alleviating m6A modifications and E2F1/MIF pathway.

Yan Mao, Feng Jiang, Xue-Jiao Xu, Lan-Bo Zhou, Rui Jin, Li-Li Zhuang, Chen-Xia Juan, Guo-Ping Zhou

Open access · goldAbstract read
In one paragraph

Article in International journal of biological sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
7.7field-weighted citation impact, top 2% 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

33 citing papers in PubMed, 47 citations in OpenAlex.

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  14. Decoding mJournal of translational medicine · 2025
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  19. YTHDF2-mediated mFrontiers in cellular and infection microbiology · 2025
    Article
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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

8 authors at 4 institutions in 1 country.

Yan MaoDepartment of Pediatrics, The First Affiliated Hospital, Nanjing Medical University, Nanjing, China.
Feng JiangDepartment of Neonatology, Obstetrics and Gynecology Hospital of Fudan University, Shanghai, China.
Xue-Jiao XuDepartment of Pediatrics, The First Affiliated Hospital, Nanjing Medical University, Nanjing, China.
Lan-Bo ZhouDepartment of Dermatology, Suzhou Hospital, Nanjing Medical University, Suzhou, China.
Rui JinDepartment of Pediatrics, The First Affiliated Hospital, Nanjing Medical University, Nanjing, China.
Li-Li ZhuangDepartment of Pediatrics, The First Affiliated Hospital, Nanjing Medical University, Nanjing, China.
Chen-Xia JuanDepartment of Nephrology, Jiangsu Province Hospital of Chinese Medicine, Affiliated Hospital of Nanjing University of Chinese Medicine, Nanjing, China.
Guo-Ping ZhouDepartment of Pediatrics, The First Affiliated Hospital, Nanjing Medical University, Nanjing, China.
Nanjing Medical University · CNNanjing University of Chinese Medicine · CNObstetrics and Gynecology Hospital of Fudan University · CNSuzhou Municipal Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Septic acute kidney injury (AKI) is characterized by inflammation. Pyroptosis often occurs during AKI and is associated with the development of septic AKI. This study found that induction of insulin-like growth factor 2 mRNA binding protein 1 (IGF2BP1) to a higher level can induce pyroptosis in renal tubular cells. Meanwhile, macrophage migration inhibitory factor (MIF), a subunit of NLRP3 inflammasomes, was essential for IGF2BP1-induced pyroptosis. A putative m6A recognition site was identified at the 3'-UTR region of E2F transcription factor 1 (E2F1) mRNA via bioinformatics analyses and validated using mutation and luciferase experiments. Further actinomycin D (Act D) chase experiments showed that IGF2BP1 stabilized E2F1 mRNA dependent on m6A. Electrophoretic mobility shift assay (EMSA) and chromatin immunoprecipitation (ChIP) indicated that E2F1 acted as a transcription factor to promote MIF expression. Thus, IGF2BP1 upregulated MIF through directly upregulating E2F1 expression via m6A modification. Experiments on mice with cecum ligation puncture (CLP) surgery verified the relationships between IGF2BP1, E2F1, and MIF and demonstrated the significance of IGF2BP1 in MIF-associated pyroptosis

Indexed as

Acute Kidney InjuryMacrophage Migration-Inhibitory FactorsNLR Family, Pyrin Domain-Containing 3 ProteinAdenosineAnimalsE2F1 Transcription FactorInflammasomesInflammationKidneyMiceRNA-Binding ProteinsRNA, MessengerAdenosineCRD-BP protein, mouseE2f1 protein, mouseE2F1 Transcription FactorInflammasomesMacrophage Migration-Inhibitory FactorsNLR Family, Pyrin Domain-Containing 3 ProteinN-methyladenosineRNA-Binding ProteinsRNA, MessengerIGF2BP1m6A RNA methylationpyroptosisseptic acute kidney injuryTranscriptional regulation

Identifiers

PMID36632449
PMCPMC9830505
OpenAlexW4313439050

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.