Evidence map›Paper›PMID 29388044›Full record

ArticleEndocrine2018

MiR-145 improves macrophage-mediated inflammation through targeting Arf6.

Rumei Li, Qiwei Shen, Nan Wu, Min He, Naijia Liu, Jinya Huang, Bin Lu, Qiyuan Yao, Yehong Yang, Renming Hu

Abstract read
PubMed Publisher
In one paragraph

Article in Endocrine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

26 citing papers in PubMed, 43 citations in OpenAlex.

  1. Trial
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  8. International journal of molecular sciences · 2023
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  15. Comparison of the Effects of Essential Oil Obtained from the Crude and Bran-ProcessedEvidence-based complementary and alternative medicine : eCAM · 2021
    Article
  16. Review
  17. Article
  18. 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

10 authors at 1 institution in 1 country.

Rumei LiDepartment of Endocrinology, Huashan Hospital, Fudan University, Shanghai, 200040, China.
Qiwei ShenDepartment of General Surgery, Huashan Hospital, Fudan University, Shanghai, 200040, China.
Nan WuDepartment of Endocrinology, Huashan Hospital, Fudan University, Shanghai, 200040, China.
Min HeDepartment of Endocrinology, Huashan Hospital, Fudan University, Shanghai, 200040, China.
Naijia LiuDepartment of Endocrinology, Huashan Hospital, Fudan University, Shanghai, 200040, China.
Jinya HuangDepartment of Endocrinology, Huashan Hospital, Fudan University, Shanghai, 200040, China.
Bin LuDepartment of Endocrinology, Huashan Hospital, Fudan University, Shanghai, 200040, China.
Qiyuan YaoDepartment of General Surgery, Huashan Hospital, Fudan University, Shanghai, 200040, China.
Yehong YangDepartment of Endocrinology, Huashan Hospital, Fudan University, Shanghai, 200040, China. yehongyang@126.com.
Renming HuDepartment of Endocrinology, Huashan Hospital, Fudan University, Shanghai, 200040, China. renminghu@fudan.edu.cn.ORCID 0000-0002-1827-3600
Fudan University · CN

Funding

National Natural Science Foundation of China 81471057National Natural Science Foundation of China (CN) 81270902
6 · The paper itself

Abstract

purposeTo explore the relationship between miR-145 and ADP ribosylation factor 6 (Arf6) in regulating macrophage-mediated inflammation.

methodsTHP-1 cells were induced by 160 nM of phorbol 12

resultsDual-luciferase reporter assays showed the direct down-regulation of Arf6 by miR-145. Forty-eight-hour-transfection of miR-145 inhibitor resulted in significant increase of Arf6, IL-1beta, TNF-alpha and IL-6 as well as phosphorylation of p65 in NF-kappaB pathway in THP-1 cells, which, inversely, were reversed by overexpressing miR-145. In addition, down-regulation of Arf6 in macrophages reduced expression and secretion of cytokines. Expression of miR-145 was found to be attenuated in the omental adipose tissue of obese patients and diabetics with greater Arf6 expression, confirming the role of miR-145 in regulating macrophage-mediated inflammation targeting Arf6.

conclusionsBy means of reducing the expression of Arf6 and subsequent signal transduction via NF-kappaB, miR-145 plays a role in inhibiting the secretion of inflammatory factors and then improving the inflammatory status. MiR-145 might be one of the candidates for anti-inflammatory treatment for metabolic diseases.

Indexed as

ADP-Ribosylation Factor 6ADP-Ribosylation FactorsHumansInflammationInflammation MediatorsInterleukin-1betaInterleukin-6MacrophagesMicroRNAsNF-kappa BPhosphorylationRNA, Small InterferingTumor Necrosis Factor-alphaADP-Ribosylation Factor 6ADP-Ribosylation FactorsARF6 protein, humanInflammation MediatorsInterleukin-1betaInterleukin-6MicroRNAsMIRN145 microRNA, humanNF-kappa BRNA, Small InterferingTumor Necrosis Factor-alphaARF6CytokineMacrophagesMetabolic inflammationMiR-145

Identifiers

PMID29388044
OpenAlexW2792169028

What OpenQuestion holds

Textmetadata
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 OpenQuestion graph.