Evidence map›Paper›PMID 31199066›Full record

ArticleJournal of cellular and molecular medicine2019

MiR-140 modulates the inflammatory responses of Mycobacterium tuberculosis-infected macrophages by targeting TRAF6.

Xiaofei Li, Shan Huang, Tingting Yu, Guiliang Liang, Hongwei Liu, Dong Pu, Niancai Peng

Open access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.5field-weighted citation impact, top 17% 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

17 citing papers in PubMed, 21 citations in OpenAlex.

  1. Review
  2. Diagnostic value and prognostic effect of has-miR-151a-3p in tuberculosis.Journal of research in medical sciences : the official journal of Isfahan University of Medical Sciences · 2026
    Article
  3. Journal of clinical tuberculosis and other mycobacterial diseases · 2024
    Review
  4. [TRAF6 promotesNan fang yi ke da xue xue bao = Journal of Southern Medical University · 2022
    Article
  5. Article
  6. Article
  7. Review
  8. Review
  9. Review
  10. Article
  11. Article
  12. MicroRNA‑502‑3p promotesMolecular medicine reports · 2021
    Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
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

7 authors at 2 institutions in 1 country.

Xiaofei LiSchool of Life Science and Technology, Xi'an Jiaotong University, Xi'an City, China.ORCID 0000-0002-0912-2050
Shan HuangDepartment of Clinical Laboratory, The Third People's Hospital of Kunming City, Kunming, China.
Tingting YuDepartment of Clinical Laboratory, The Third People's Hospital of Kunming City, Kunming, China.
Guiliang LiangDepartment of Clinical Laboratory, The Third People's Hospital of Kunming City, Kunming, China.
Hongwei LiuDepartment of Clinical Laboratory, The Third People's Hospital of Kunming City, Kunming, China.
Dong PuDepartment of Clinical Laboratory, The Third People's Hospital of Kunming City, Kunming, China.
Niancai PengSchool of Life Science and Technology, Xi'an Jiaotong University, Xi'an City, China.
Kunming Third People's Hospital · CNXi'an Jiaotong University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study aimed to examine miR-140 expression in clinical samples from tuberculosis (TB) patients and to explore the molecular mechanisms of miR-140 in host-bacterial interactions during Mycobacterium tuberculosis (M tb) infections. The miR-140 expression and relevant mRNA expression were detected by quantitative real-time PCR (qRT-PCR); the protein expression levels were analysed by ELISA and western blot; M tb survival was measured by colony formation unit assay; potential interactions between miR-140 and the 3' untranslated region (UTR) of tumour necrosis factor receptor-associated factor 6 (TRAF6) was confirmed by luciferase reporter assay. MiR-140 was up-regulated in the human peripheral blood mononuclear cells (PBMCs) from TB patients and in THP-1 and U937 cells with M tb infection. Overexpression of miR-140 promoted M tb survival; on the other hand, miR-140 knockdown attenuated M tb survival. The pro-inflammatory cytokines including interleukin 6, tumour necrosis-α, interleukin-1β and interferon-γ were enhanced by M tb infection in THP-1 and U937 cells. MiR-140 overexpression reduced these pro-inflammatory cytokines levels in THP-1 and U937 cells with M tb infection; while knockdown of miR-140 exerted the opposite actions. TRAF6 was identified to be a downstream target of miR-140 and was negatively modulated by miR-140. TRAF6 overexpression increased the pro-inflammatory cytokines levels and partially restored the suppressive effects of miR-140 overexpression on pro-inflammatory cytokines levels in THP-1 and U937 cells with M tb infection. In conclusion, our results implied that miR-140 promoted M tb survival and reduced the pro-inflammatory cytokines levels in macrophages with M tb infection partially via modulating TRAF6 expression.

Indexed as

3' Untranslated RegionsBase SequenceCytokinesHumansInflammationInflammation MediatorsMacrophagesMicrobial ViabilityMicroRNAsMycobacterium tuberculosisRNA, MessengerTHP-1 CellsTNF Receptor-Associated Factor 6U937 CellsUp-Regulation3' Untranslated RegionsCytokinesInflammation MediatorsMicroRNAsMirn140 microRNA, humanRNA, MessengerTNF Receptor-Associated Factor 6human peripheral blood mononuclear cellsmiR-140M tb survivalMycobacterium tuberculosispro-inflammatory cytokinesTRAF6

Identifiers

PMID31199066
PMCPMC6653720
OpenAlexW2950288456

What OpenQuestion 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 OpenQuestion graph.